Jobs at UCB Pharma

Principal Statistical Methodologist (Raleigh, North Carolina, US)

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We are looking for a Principal Statistical Methodologist who is curious, collaborative, and strategic to join our Statistical Innovation team within Biometric and Data Sciences (BDS), based in Raleigh (US).

About the role
You will help shape how evidence is generated and communicated across the drug development lifecycle—from early clinical development to regulatory approval and lifecycle work. You will provide expert statistical consultation on trial design and analysis, develop and apply advanced methods, and translate complex quantitative concepts into clear insights for cross-functional partners. You will also contribute to scientific communications and external collaboration through publications and industry initiatives.

Who you will work with
You will be part of a team that provides statistical consultancy across therapy areas and development stages, partnering closely with colleagues in clinical development, regulatory strategy, data science, and medical affairs. The team values curiosity and problem solving, practical innovation, clear communication, and collaboration—bringing novel statistical approaches into real study decisions and sharing learnings with the wider scientific community.

What you will do

Provide statistical consultation on clinical trial design and analysis across multiple development stages and therapy areas.
Develop and implement innovative statistical approaches, including model-based methods using frequentist and Bayesian techniques.
Run or guide advanced analyses and simulations to inform design options, sample size, and power trade-offs.
Communicate complex quantitative topics clearly using visuals, simulations, and plain language for diverse audiences.
Contribute to internal learning by delivering training on advanced statistical concepts for non-statisticians and statisticians.
Contribute to the group’s external profile through scientific publications, conference presentations, and participation in cross-industry initiatives and working groups.

Interested? Here is what we are looking for

Doctoral degree in statistics, mathematics, or a closely related scientific discipline.
3+ years of experience working in biostatistics within the pharmaceutical industry. Experience in statistical methodology for clinical development (early to late stage) is an advantage.
Expertise in advanced statistical methods and innovative trial design; experience with causal inference and estimands is an advantage.
Strong statistical programming skills (R preferred; equivalent tools considered).
Sound knowledge of ICH guidelines and understanding of regulatory requirements from major health authorities.
Ability to work effectively with autonomy, manage multiple priorities, and deliver timely, high-quality outputs.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Medical Science Liaison / Florida Region (Miami, Florida, US)

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UCB is looking for an experienced, science-driven and patient-focused Medical Science Liaison (MSL) to work with the Myasthenia Gravis Team to strengthen our neurological Rare Disease Organization’s (RDO) mission for the team in the Florida Region, which currently includes Florida, Alabama coastal region & Puerto Rico.

About the Role

The MSL provides peer-level scientific exchange with clinicians and researchers working in neuromuscular diseases. This role fosters collaborative, science-driven partnerships with key stakeholders to support optimized patient care. The MSL will provide scientific exchange, contribute insights to medical strategies, and drive patient-focused initiatives within the local health ecosystem.

Who you will work with

Internal partners: Medical Affairs (including Medical Directors), Real-World Evidence (RWE), Clinical Development/Operations, Medical Information, Compliance/Legal, and cross-functional commercial colleagues (e.g., sales, marketing, market access).

External partners: healthcare providers and key opinion leaders (KOLs), clinical investigators, medical decision-makers in health systems/IDNs, and patient advocacy organizations.

What you’ll do

Maintain deep therapeutic-area expertise by staying current on pre-clinical and clinical data, treatment options, emerging standards of care, and competitive landscape for myasthenia gravis and other neuromuscular disorders.

Develop and manage trusted, peer-to-peer relationships with key stakeholders (e.g., KOLs, clinical investigators, medical groups/IDNs, patient advocacy groups) and execute tailored engagement plans to identify local needs and opportunities.

Deliver balanced scientific exchange and clinical value propositions, including addressing medical information inquiries and providing effective, audience-tailored presentations to internal and external audiences.

Generate and communicate meaningful medical insights from the field to inform medical strategy and tactics, including input for creation and updates of Standard Response Letters.

Represent UCB as a scientific expert at local, regional, and national conferences where issues related to the diagnosis and treatment of neuromuscular diseases are addressed.

Identify and support research and educational collaboration opportunities, including feasibility assessment and primary liaison support for unsolicited Investigator-Initiated Studies (IIS) from inception through publication.

Collaborate cross-functionally (e.g., Medical, RWE, access, and other partners) to enhance patient care, support access engagements with medical expertise as needed, and contribute to broader Medical Affairs projects.

Interested? For this position, you'll need the following education, experience and skills:

Minimum Qualifications:

Doctoral level degree (PharmD, PhD, MD, DO, or DNP); Nurse Practitioners with research and/or clinical expertise in a related field and advanced training/education may be considered.

Minimum 1+ years of medical affairs experience in the biopharmaceutical industry.

Must reside within the assigned territory.

Valid driver’s license and ability to travel up to 80% in the designated territory.

Preferred Qualifications:

Relevant therapeutic area experience in neurology, neuromuscular, and/or rare diseases
Bilingual: Spanish/English

Strong business acumen with a solid understanding of the pharmaceutical industry.

Ability to clearly articulate complex scientific concepts in 1:1 and group settings.

Basic knowledge and understanding of health, economic principles and clinical trials.

Experience in partnership with Global and local therapy area experts and external organizations

Must be a strong team player and effectively interface with other internal departments including regional business units, marketing, sales, medical affairs, and clinical operations.

Creative approach to problem solving and able to work effectively in a constantly changing environment.

Strong interpersonal skills and excellent verbal and written communication skills.

Strong time management and organizational skills with proficiency in Microsoft applications.

Ability to work independently and manage a large territory with multiple stakeholders

This position's reasonably anticipated base salary range is $156,000.00-$204,000.00 annually. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Associate Director, US Federal Government Affairs (Washington, District of Columbia, US)

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We are looking for a Associate Director, U.S. Federal Government Affairs who is strategic, collaborative, and results-driven to join our U.S. Government Affairs & Public Policy (GAPP) team, based in our Washington, DC office.

About the role

You will be responsible for initiating and executing comprehensive strategies to engage with federal policymakers to help advance public policies that support patients’ access to innovative therapies. You will work across complex legislative environments, building relationships and influencing policy outcomes that align with patient-focused priorities.

Who you’ll work with

You will collaborate closely with colleagues across corporate affairs, regulatory, commercial, and market access functions, as well as external partners including policymakers, trade associations, and coalitions. You’ll be part of a highly collaborative team focused on aligning priorities and driving meaningful impact for patients.

What you’ll do

Represent UCB before the U.S. Congress and the Executive Branch on company specific issues as well as issues of importance to the biopharma industry.
Shape policy strategies supporting access to innovative therapies
Monitor federal policy trends and assess business impact
Collaborate internally to align priorities across functions
Engage trade associations and external partners to influence decisions
Help manage federal engagement by UCB lobbying consultants
Communicate policy developments and insights to key stakeholders
Participate in political fundraisers on behalf of UCB’s political action committee. Outreach to eligible employees to encourage participation in PAC membership.

Interested? For this role we’re looking for the following

Minimum requirements

Bachelor’s degree required; advanced degree preferred
8–10 years federal policy or Capitol Hill experience
Experience in healthcare public policy at the federal level
Strong communication and stakeholder management skills
Ability to manage multiple priorities independently
Proven ability to build relationships and drive collaboration

Preferred requirements

Strong research and analysis skills in public policy, particularly health care
Advanced problem-solving and analytical capabilities
Strong written communication and presentation skills
Established network within Congressional offices and policy stakeholders, particularly Republican offices
Comfort and ability to present information internally and externally on behalf of UCB

This positions reasonably anticipated base salary range is $148,000-194,300. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Marketing Solutions Lead, Rare Disease (Oakville, Ontario, CA)

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We are looking for a Rare Disease Marketing Solutions Lead with a proven track record of providing commercial and marketing leadership to join our Rare Disease Organization based out of our office in Oakville, ON

About the role

This critical business leadership role will evaluate, build and execute best in class integrated strategic plans for a portfolio of target treatments approved for generalized Myasthenia Gravis (gMG). This individual will maintain a very high level of category knowledge including but not limited to product / treatment landscape, patient journey and market access to design marketing plans that will drive business goals. This role will collaborate with members of the Rare Disease cross functional team to build and lead the strategy, create programs and materials that are executed with excellence to deliver patient value and allow UCB to achieve its financial and non-financial objectives over the life of the franchise.

Who you’ll work with

As part of a multidisciplinary team, you’ll partner with all internal stakeholders to build best in class market plans. You will partner with external stakeholders via commercial consultations to build go-to-market strategies and tactics that are clinically relevant.

What you’ll do

Set the Canadian patient and financial ambition for rare assets through deep understanding and collaboration with cross-functional partners, including sales, medical, finance, PSP, regulatory, and supply chain.
Create integrated brand and portfolio business plans that result in strategic initiatives and tactical programs that maximize the value of the brands in the marketplace.
Develop commercial execution strategies consistent with Global and Regional brand strategy for 2 products that will optimize brand and UCB’s portfolio position in the Canadian marketplace
Lead and execute a strategic KOL engagement and commercial advisory board / consult plan, generating high impact insights and incorporating these into the brand plans and commercial strategies
Guide and monitor the most impactful quantitative and qualitative performance measures, inclusive of financial, market, and operational execution to ensure delivery on the plans.
Analyze and integrate market data to derive insights that drive the development of strategic plans
Champion customer excellence through all channels and create high quality, high impact, individualized omnichannel plans to drive growth.
Lead a marketing vision for digital care transformations and pilots or projects that would create health system change for patients.
Manage OPEX budget associated with program development and execution.
Provide leadership to develop the next generation of leaders at UCB.

Qualifications

Bachelors’ degree in health sciences, business or related field is required.
Minimum 10+ years in pharmaceutical industry, with track record of progressive experience
Minimum 5+ years biopharma product leadership and launch experience on complex, Rare Disease products required.
Leadership experience in specialty / biologic commercial strategy and execution
Deep understanding of market access environment for specialty/biologic or rare (preferred)
Product launch experience required.
Specialty sales experience is strongly preferred.
Demonstrated leadership skills, with a proven ability to drive results and act with a sense of urgency and accountability, are essential. We are seeking a proactive leader who inspires teams and delivers outcomes efficiently and effectively.
Bilingual (English/French) is considered an asset; Experience in Neurology and/or Rare Disease preferred.
Travel is required (15-20%) – Congress, Advisory Board Meetings, Territory and Stakeholder field visits.

This positions reasonably anticipated base salary range is $150,000 - $180,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

We’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

We are committed to fostering an inclusive, accessible environment, where all employees and members feel valued, respected, and supported. We are committed to meeting the accessibility needs of persons with disabilities.

If you require an accommodation for the recruitment/interview process (e.g. alternate formats of materials, accessible meeting rooms or other accommodation), please contact HRAnswers@ucb.com and we will work with you to meet your needs.

Please note that our hiring process includes the use of artificial intelligence (AI). All final hiring decisions are made by our hiring teams.

Downstream Manager (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Downstream Manager who is an inspiring leader, operationally strong, and quality‑driven to join our Clinical Manufacturing Sciences team, based at our UCB campus located in Braine‑l’Alleud, Belgium.

About the role
In this role, you are going to lead Downstream and Buffer Production activities within our Biologics Pilot Plant. You will also ensure safe, compliant, and efficient cGMP manufacturing of Drug Substance for clinical trials (Phases I–III). You will combine people leadership, operational excellence, and continuous improvement to deliver high‑quality results while preparing our operations for future growth.

Who you will work with
You will work closely with a passionate Downstream Production team and collaborate daily with Quality, Validation, Engineering, Process Development, and external partners. You are going to be part of a cross‑functional, international environment where teamwork, knowledge sharing, and trust are at the core of everything we do.

What you will do

Lead and develop a ~30‑person Downstream Production team, fostering performance, engagement, resilience, and strong team spirit.
Ensure safe, compliant, and OTIF delivery of Drug Substance for Phase 1–3 clinical programs through robust cGMP downstream operations.
Oversee purification, TFF, chromatography, and Drug Substance filling activities while resolving daily operational issues and supporting effective decision‑making.
Drive quality excellence through solid documentation practices, deviation management, investigations, and CAPA execution.
Promote continuous improvement, operational excellence, cost optimization, and adaptable planning in a fast‑changing manufacturing environment.
Support technology transfer, scale‑up, and implementation of new processes/equipment through close cross‑functional collaboration.

Interested? For this role we're looking for the following education, experience and skills

For this role, we are looking for the following education, experience, and skills:

Master’s degree in Life Sciences, Engineering, or a related scientific field.
Proven leadership experience in biologics or pharmaceutical manufacturing.
Strong knowledge of Downstream processing and cGMP environments.
Ability to drive continuous improvement and data‑based decision making.
Excellent communication, collaboration, and stakeholder management skills.
Fluency in English and French.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Group Leader Neuroinflammation (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Senior Leader in Neuroimmunology Research who is passionate, inspiring and scientifically driven to join us in our Neuroinflammation research team, based in our Braine-l’Alleud office in Belgium.

About the role

You will lead a key expansion area within our neuroimmunology strategy, focusing on how peripheral immune mechanisms influence neurological disease of the peripheral and central nervous systems. You will shape scientific direction, build and lead a high-performing team, and drive the identification and progression of new therapeutic targets. This is a highly visible role where your leadership, scientific excellence and ability to translate research into impactful solutions will directly contribute to advancing our pipeline of innovative treatments.

Who you’ll work with

You will be working in a team that brings together cross-functional experts across neuroinflammation research, collaborating closely with internal stakeholders and external partners from academia and biotechnology. You will interact with scientific leaders, translational specialists and project teams to define and deliver research strategies. You will also build and manage partnerships externally, ensuring strong alignment and impact across the broader scientific ecosystem.

What you’ll do

Lead research strategy in peripheral neuroimmunology and immune-driven neurological diseases
Build, lead and develop a high-performing team of scientists
Drive pipeline projects from target identification to candidate selection
Translate immune biology insights into therapeutic strategies and drug targets
Establish collaborations with academic, biotech and external research partners
Provide scientific leadership across projects and influence cross-functional decisions

Interested? For this role we’re looking for the following education, experience and skills

PhD in immunology, neuroimmunology or related scientific discipline
Proven industry experience in pharmaceutical or biotechnology environments
Expertise in peripheral immune biology within neurological disease context
Experience leading scientific teams and delivering pipeline projects
Strong passion, leadership, communication and stakeholder engagement skills
Ability to translate complex science into impactful research strategies

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Physical Asset Manager (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Global Physical Asset Manager – Biopharma Equipment who is strategic, collaborative, and impact-driven to join our team Global Physical Asset Management Department, based at our UCB campus located in Braine-l’Alleud, Walloon Brabant, Belgium.

About the role

You will oversee the global lifecycle performance of biopharma equipment, ensuring safety, compliance, and efficiency. You will develop a comprehensive view of asset health, risks, and investment needs to optimize total cost of ownership across CAPEX and OPEX and support UCB’s strategy. You will act as a key driver of asset management practices across research, development, and manufacturing environments.

Who you will work with

You will collaborate with cross-functional and international teams, including asset owners, engineering, maintenance, HSE, finance, and external partners. You will also engage with global asset management colleagues to ensure consistency in standards, tools, and methodologies across sites.

What you will do

• You will deploy asset management strategies across manufacturing, development, and clinical sites.
• You will ensure data consistency and reliability within asset registers and reporting tools.
• You will lead equipment assessment programs for safety, compliance, and performance.
• You will manage technical risks and drive mitigation strategies with stakeholders.
• You will develop asset performance insights to support investment and budget decisions.
• You will drive change and foster new ways of working across global teams.

Interested? For this role, we are looking for the following education, experience, and skills:

• You hold a Master’s degree and 10+ years’ experience in pharma, biologics, or medical device manufacturing.
• You bring experience in asset, risk, or maintenance management programs.
• You demonstrate strong project or program management capabilities.
• You can lead cross-functional teams in complex, matrix, multicultural environments.
• You communicate effectively with technical experts and senior leadership.
• You show strategic thinking, influence skills, and a forward-looking mindset.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Physical Asset Manager - Biologics Manufacturing (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

About the role

Who you will work with

What you will do

Interested? For this role, we are looking for the following education, experience, and skills:

• You hold a Master’s degree and 10+ years’ experience in pharma, biologics, or medical device manufacturing.
• You bring experience in asset, risk, or maintenance management programs.
• You demonstrate strong project or program management capabilities.
• You can lead cross-functional teams in complex, matrix, multicultural environments.
• You communicate effectively with technical experts and senior leadership.
• You show strategic thinking, influence skills, and a forward-looking mindset.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Development Quality Ops Data Integrity Partner (Braine L'alleud, Walloon Brabant, BE)

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To strengthen our Clinical Manufacturing Quality department we are looking for a talented profile to fill the position of: Development Quality Operations Data Integrity Partner – Braine l’Alleud, Belgium.

About the role
As part of Clinical Manufacturing Quality, you act as a Dev Quality Lab Ops Data Integrity Partner supporting CMC Development Sciences and Clinical Supply Chain entities. Your primary responsibility is to ensure the establishment, implementation, maintenance and continuous improvement of an effective Quality Management System (QMS) and robust Data Integrity practices across product development, from early clinical phases through to commercialization. This includes providing GMP oversight of laboratories at the Braine site in Belgium and GxP oversight of development entities across the Braine-l’Alleud and UK (e.g. Slough) campuses.

You will work with
In this role, you closely support the Labs & Dev Compliance Quality Lead by contributing to global quality oversight of clinical manufacturing and supply activities, working in close collaboration with both internal (Braine, Slough, Leuven) and external stakeholders.

What you will do

Compliance Support: Ensuring adherence to GMP/GDP regulations, health and safety guidelines.
Data Integrity Management: Active participation in QA forums and lead meetings to manage Data Integrity (DI).
Documentation Systems: Supporting and maintaining compliant documentation processes for UCB development activities.
Issued Copy Process: Acting as Reconciler to verify correct completion of the “issued copy” process and coordinating local instructions with stakeholders to maintain common practices.
Training: Providing GMP/GDP expertise and data integrity training to customer department members.
QA Dev Compliance Oversight: Ensuring QMS compliance with regulations and policies, coordinating daily QA systems and DI activities.
Data Integrity Governance: Leading CMC and CSC data integrity alignment, reviewing risk assessments, remediation plans, and effectiveness checks.
Audit Management: Coordinating audit preparedness, managing responses to audit observations including CAPA activities.
Continuous Improvement: Driving improvement opportunities related to QMS, Data Integrity, and Documentation Control; supporting digitalization initiatives.
Stakeholder Interface: Acting as the operational link between QA-Systems, CMC Development, Clinical Supply Chain, IT, and QA-Management; preparing compliance, KPI, and risk summaries.
Backup Function: Serving as backup for the Dev Quality Lab Ops Partner to ensure continuity in QA Lab Oversight.
Guidance and Issue Resolution: Providing expert advice on GMP regulations, identifying and resolving compliance and quality issues to support training and improvements.
Support for Development Quality Lead: Assisting with laboratory/manufacturing quality systems activities such as deviation closeout, change management, complaints, and quality improvement.
Coaching and Training: Delivering regular data integrity training and coaching across CMC Development and CSC entities

Interested? For this position you’ll need the following education, experience and skills

Bachelor’s, master’s degree or an education in a relevant scientific discipline
At least 5 years’ experience in a QA regulated pharmaceutical environment
Fluent in French and English communication (oral and written); any additional languages are a plus.
Strong knowledge of regulatory requirements (FDA, EudraLex, PIC/S, ICH)
Experience in audit and inspection support
Exhibit effective communication skills when interacting with stakeholders
Capable of working independently and taking initiative
Must be able to act in most circumstances without direct supervision and handle complex/urgent situations.
Analytical and problem-solving capabilities

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Principal Statistical Methodologist (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

What you will do

Provide statistical consultation on clinical trial design and analysis across multiple development stages and therapy areas.
Develop and implement innovative statistical approaches, including model-based methods using frequentist and Bayesian techniques.
Run or guide advanced analyses and simulations to inform design options, sample size, and power trade-offs.
Communicate complex quantitative topics clearly using visuals, simulations, and plain language for diverse audiences.
Contribute to internal learning by delivering training on advanced statistical concepts for non-statisticians and statisticians.
Contribute to the group’s external profile through scientific publications, conference presentations, and participation in cross-industry initiatives and working groups.

Interested? Here is what we are looking for

Doctoral degree in statistics, mathematics, or a closely related scientific discipline.
3+ years of experience working in biostatistics within the pharmaceutical industry. Experience in statistical methodology for clinical development (early to late stage) is an advantage.
Expertise in advanced statistical methods and innovative trial design; experience with causal inference and estimands is an advantage.
Strong statistical programming skills (R preferred; equivalent tools considered).
Sound knowledge of ICH guidelines and understanding of regulatory requirements from major health authorities.
Ability to work effectively with autonomy, manage multiple priorities, and deliver timely, high-quality outputs.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of Global Compensation (Anderlecht, Brussels, BE)

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We are looking for a forward-thinking Head of Global Compensation who will redefine how we design, deliver, and continuously evolve our reward strategy, in support of our Patient Value Strategy, on a global scale. This is an exciting opportunity for a professional who is strategic, collaborative, and data-driven to join us in our HR Operations & Global Reward leadership team, based in our Brussels office in Belgium.

About the role

You will play a pivotal role in strengthening the foundations of our reward architecture while accelerating digital transformation and automation across the function. Your mandate is to build a future-ready compensation ecosystem - data-driven, scalable, deeply aligned with business strategy.

You and your team will lead the design and delivery of our Global Compensation Strategy, ensuring it supports business goals and attracts, engages, and retains talent. You will drive competitive, equitable, and transparent reward practices. This is a key leadership role with a strong focus on governance, analytics, and continuous improvement across compensation policy and frameworks.

Who you’ll work with

As part of the Global Reward Center of Expertise, you will work within a team that partners closely with Human Resources colleagues, business leaders, digital and technology teams, legal, and finance across multiple markets. You will also collaborate with external partners to benchmark and strengthen our reward practices in support of our reward principles.

What you’ll own

The development and execution of Global Compensation Strategy aligned with organizational goals and leading market practices, ensuring consistency, competitiveness, and simplicity across regions and business areas
Design of competitive and inclusive reward frameworks in partnership with senior stakeholders across UCB and external experts
Modernization of compensation processes and tools, driving automation, digitization, and improved employee and manager experience
In partnership with IT and digital teams, the design and implementation of scalable, integrated reward solutions (e.g., platforms, analytics, AI-enabled insights)
Building out strong data and analytics capabilities to inform decision-making and elevate compensation as a strategic lever
Innovative scalable approaches through pilots and experimentation - continuously improving effectiveness and efficiency
Robust governance and compliance practices that promote fair and equitable pay practices across all regions while simplifying frameworks and enhancing usability
Leadership, mentoring, and development of an effective and engaged global compensation team and indirectly, ensure a strong local reward delivery network.
Robust annual compensation cycles, including salary review, short and long term incentives and recognition programs.

What sets you apart?

For this role we’re looking for:

A future-oriented compensation/rewards leader with a global mindset, capable of operating across diverse markets with complexity and nuance
A track record of designing and transforming reward functions at scale in global & regional setups
Strong digital and data acumen, with the ability to bridge HR, IT, and data ecosystems
Strong analytical skills with the ability to translate data into actionable business insights.
A proven change agent, comfortable challenging established practices and driving adoption of new ways of working
Recognized ability to lead through influence at all levels and position Compensation as a critical business driver
A leadership style grounded in empathy and active listening, enabling integration of diverse perspectives, taking principle-based decisions and building trust across stakeholders
A strong commitment to inclusive leadership, ensuring fair, equitable, and transparent reward practices
A highly collaborative approach, working seamlessly across HR, IT, and business teams to co-create impactful solutions
Knowledge of pharma industry preferred, or adjacent, high expertise-driven industry.
Strong knowledge of regulatory requirements and best practices in pay equity and transparency.
Strong academic and/or professional background in Human Resources, Business, Finance, Legal, Economics, or a related discipline, combined with deep global compensation expertise.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Regulatory CMC Scientist (Anderlecht, Brussels, BE)

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We are looking for a Regulatory CMC Scientist to join us in our Global Regulatory team, based in any of our Brussels (Belgium), Slough (UK) or Raleigh/Atlanta (US) offices.

About the role

Define the strategy, planning and preparation (writing and review) of CMC submission documentation for regulatory submissions (new marketing applications, variations) from a global/regional perspective to achieve timely approvals to meet business needs.

Who you’ll work with

You will work within the Regulatory CMC team and partner with other technical and regulatory functions across the business.

What you’ll do

Responsible for regional and global CMC submissions in line with agreed global regulatory strategy, and within agreed timelines.

Contribute and ensure adequate provision of regulatory CMC input to all Health Authority (HA) interactions on CMC matters in all regions

Ensures effective communication of CMC regulatory strategy, risks, and overall plan to GRA Teams, Technical, Development and Commercial Teams

Highlights anticipated and ongoing critical issues arising through the product life cycle in a timely manner to senior management to enable communication to key stakeholders

Lead or contribute to ongoing process improvement and department initiatives within the CMC Regulatory Affairs function, including process improvements, SOP review and development, and evaluation/implementation of digital strategies and tools.

Interested? For this position you’ll need the following education, experience and skills:

Bachelor’s degree, Master’s preferred in a relevant life science or business-related discipline

Demonstrated ability to leverage digital tools, structured data, and regulatory information systems to enhance CMC and Device regulatory strategy, submission quality, lifecycle management, and decision‑making across global markets

Significant relevant experience in the pharmaceutical industry preferably in Regulatory Affairs CMC with focus on biological entities

Proven track record of successful authoring and contribution to delivering CMC sections of marketing authorisations for new biological entities

Knowledge of GMP requirements, standard systems (e.g. change management systems and tools)

Effective interpersonal, presentation and communication skills with established internal and external stakeholders

Proven leadership, problem-solving ability, flexibility, influence, and effective teamwork skills.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien.ne Biomanufacturing - Media & Buffer (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons plusieurs Technicien.nes Biomanufacturing – Media & Buffer (semaine shift de jour) talentueux.ses et motivé.es pour rejoindre notre Belgium Biomanufacturing Operations Center à Braine-L’Alleud, Belgique.

Ici, vous pouvez réellement enrichir votre expertise dans un environnement dynamique et porteur, où votre épanouissement et votre développement sont prioritaires. En travaillant avec les technologies les plus récentes et des techniques inédites, vous contribuerez à produire des médicaments révolutionnaires pour apporter des améliorations réelles aux patients, aujourd’hui et à l’avenir.

Le rôle s’effectue à 100% sur site et comprend des horaires en shift, du lundi au vendredi (6h-14h et 14h-22h).

Concernant le rôle :

Vous contribuerez aux opérations de fabrication biotechnologique, de la préparation des milieux et tampons à la culture et purification des biomolécules, dans le respect des standards qualité, sécurité et réglementaires.

Vous travaillerez avec :

Vous intégrerez une équipe compétente et dynamique et interagirez quotidiennement avec l’ensemble des fonctions en charge du développement de notre nouvelle usine de production biotech.

Vos activités :

Réaliser les opérations de production conformément aux procédures
Mettre en service, surveiller et nettoyer les équipements
Ajuster les paramètres critiques du procédé
Produire des lots commerciaux en respectant les GMP (Good Manufacturing Practice)
Participer aux réunions opérationnelles et maintenir la zone de travail
Contribuer aux projets
Effectuer le nettoyage des locaux, la maintenance de premier niveau et les contrôles en cours de fabrication
Soutenir la réalisation des objectifs de l’équipe et assurer la coordination en cas d’absence du responsable
Identifier et signaler les risques liés à la sécurité, qualité ou délais
Initier des déviations qualité et participer aux audits internes/externes
Documenter rigoureusement les activités dans les systèmes
Respecter et promouvoir les bonnes pratiques de sécurité
Suivre le plan de formation et proposer des améliorations
Contribuer à l’amélioration continue et à l’intégration des nouveaux membres
Assurer la liaison avec les intervenants internes/externes pour les activités quotidiennes

Intéressé.e ? Pour ce poste, nous recherchons la formation, l’expérience et les compétences suivantes :

Expérience en production biotech ou pharma
Une précédente expérience en Media & Buffer est vivement souhaitée
Bonne connaissance des GMP (Good Manufacturing Practice)
Excellent esprit d’équipe et capacité à prendre des initiatives
Prise de décision et responsabilité à son niveau
Capacité à travailler dans un environnement dynamique et à gérer les urgences
Maitrise du français

#Biomanufacturing

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

UCB est une société biopharmaceutique mondiale, spécialisée dans la neurologie et l'immunologie. Nous sommes plus que 9.000 personnes aux quatre coins du monde, inspirées par les patients et motivées par la science.  

Pourquoi travailler pour nous ?

Chez UCB, nous ne nous limitons pas à réaliser des tâches, nous créons de la valeur. Nous ne craignons pas d'aller de l'avant, de collaborer et d'innover pour faire la différence auprès des patients. Nous avons une culture de bienveillance et solidarité où chacun se sent inclus, respecté et a des chances égales de faire de son mieux. Nous allons au-delà pour créer de la valeur pour nos patients, et toujours dans une optique humaine, que ce soit pour nos patients, nos employés ou notre planète. En travaillant pour nous, vous découvrirez un monde où vous pourrez grandir et aurez la liberté de tracer votre propre parcours professionnel et accomplir votre plein potentiel.

Chez UCB, nous avons adopté une approche hybride du travail, réunissant les équipes dans des hubs locaux pour favoriser la curiosité collaborative. Sauf mention contraire dans la description du poste ou incompatibilité avec ses missions, ce poste est hybride, avec 40 % du temps de travail effectué au bureau.

UCB est un employeur qui promeut l'égalité des chances. Toutes les décisions d'embauche seront prises sans tenir compte de toute caractéristique protégée par les lois applicables. Si vous avez besoin d'ajustements à notre processus de recrutement afin de mettre en valeur vos compétences, veuillez nous contacter à l'adresse EMEA-Reasonable_Accommodation@ucb.com. À noter que si votre message ne concerne pas une demande d'ajustements, nous ne pourrons pas vous assister par ce biais.

VIE_CPLO Digital Operations & Process Improvement Associate (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

UCB est une entreprise biopharmaceutique internationale ayant pour activités principales la recherche, le développement et la commercialisation de produits pharmaceutiques et biotechnologiques. Elle est spécialisée dans la recherche de solutions thérapeutiques pour des patients souffrant de maladies sévères, traitées par des spécialistes, plus particulièrement dans le domaine du système nerveux central (en ce compris l'épilepsie) et des inflammations (y compris les allergies).

Le site de Braine-l’Alleud est spécialisé dans la synthèse chimique, le développement, la fabrication et le conditionnement de produits pharmaceutiques.

Pour plus d’information : www.ucb.com

Votre mission consistera en:

Contribuer à l’amélioration continue de la performance opérationnelle des activités de conditionnement clinique et de logistique, dans un environnement GMP exigeant.
Développer des supports de formation innovants afin de renforcer la culture GMP et favoriser l’adoption des bonnes pratiques.
Formaliser, standardiser et digitaliser les processus opérationnels et documentaires.
Améliorer les outils de pilotage, de planification et les tableaux de bord de suivi de performance.
Assurer le suivi, la structuration et le reporting des plans d’actions liés aux initiatives d’amélioration continue.
Participer activement à des projets transversaux visant la transformation des processus, l’optimisation opérationnelle et l’amélioration de la performance globale.
Evoluer dans un contexte offrant une exposition à la fois opérationnelle et stratégique, avec une autonomie croissante.

Votre profil :

Formation supérieure (école d’ingénieur, supply chain, pharmacie, business ou équivalent).
Intérêt marqué pour les environnements opérationnels, complexes et fortement réglementés (type GMP).
Solides capacités d’analyse, de synthèse et de structuration.
Appétence pour l’amélioration continue et la digitalisation des processus.
Bonne maîtrise des outils digitaux et aisance dans la gestion et l’analyse de données.
Excellentes compétences en communication, avec capacité à interagir avec des interlocuteurs variés.
Esprit d’initiative, curiosité et orientation solution.
Français courant et anglais intermédiaire avancé, permettant d’évoluer dans un environnement partiellement anglophone.

Merci de bien vouloir noter que les conditions strictes d’éligibilité à ce programme sont les suivantes :

Avoir entre 18 et 28 ans;
Détenir la nationalité d’un pays membre de l’Espace Economique Européen;
Ne pas avoir travaillé ou vécu dans le pays où aura lieu la mission;
Etre disponible pour se consacrer à la mission à temps plein;
Si vous êtes de nationalité ou de double nationalité française, être en règle vis à vis des obligations de service national de la France (Numéro Identifiant Défense);
Avoir un casier judiciaire vierge.

Si vous ne remplissez pas l'ensemble de ces conditions, nous ne pourrons pas tenir compte de votre candidature.

VIE Bioanalytical Scientist (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

UCB is an international biopharmaceutical company primarily engaged in the research, development, and commercialization of pharmaceutical and biotechnological products. It specializes in researching therapeutic solutions for patients suffering from severe diseases, treated by specialists, particularly in the fields of the central nervous system (including epilepsy) and inflammation (including allergies). 

The Braine-l'Alleud site specializes in chemical synthesis, development, manufacturing, and packaging of pharmaceutical products.

More information at: www.ucb.com 

Your mission:

We are looking for a junior scientist to join the Bioanalysis team within the Precision Medicine department in Braine-l’Alleud. You will contribute to the development of pharmacokinetic (PK) bioanalytical methods, primarily using Ligand Binding Assays (LBA, MSD platform), with potential exposure to LC-MS, to support the transition of drug candidates into clinical development.

Key responsibilities:

Participate in the development, optimization, and troubleshooting of bioanalytical methods (mainly LBA).
Build an understanding of PK bioanalysis and its role in NBE projects.
Contribute to laboratory activities, from method development to data analysis and interpretation.
Collaborate with multidisciplinary teams.
Apply good laboratory practices, quality requirements, and data integrity standards.
Gradually develop autonomy in a dynamic and supervised environment.

Your profile :

Minimum a Bachelor’s degree, with experience in LBA and/or mass spectrometry (other laboratory techniques are also considered).
Position based in Braine-l’Alleud for a duration of 12 months, with possible extension.
Contribution to the development of pharmacokinetic (PK) assays, primarily using LBA technologies (MSD), with potential exposure to LC-MS.
Participation in bioanalytical development activities: method setup, optimization, and data analysis.
Integration into the bioanalysis laboratory with progressive development towards increased autonomy in experimental work and results interpretation.

Please note that this program is in partnership with Business France, and we follow the prerequisites required by Business France to carry out a VIE assignment. The main participation prerequisites are as follows:

Be between 18 and 28 years old;

Hold the nationality of a member country of the European Economic Area;

Have not worked or lived in the country where the mission will take place;

Be available to dedicate yourself to the mission full-time;

If you have French nationality or dual nationality, be in compliance with the national service obligations of France (Numéro Identifiant Défense);

Have a clean criminal record.

If you do not meet all these conditions, we will not be able to consider your application.

Material Planner (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Material Planner who is organized, proactive and collaborative to join us in our Clinical Manufacturing team, based in our Braine-l’Alleud campus, in Belgium.

About the role

You will be working in a team that ensures the timely supply of materials needed to support manufacturing activities. You will coordinate material planning, procurement, and stock management to enable smooth production operations while minimizing risks and ensuring compliance.

Who you’ll work with

You will work closely with supply chain colleagues, quality teams, production teams, and external suppliers. The role involves daily collaboration with multiple stakeholders to ensure materials are available and aligned with production needs.

What you’ll do

Coordinate material planning from forecasting to delivery, ensuring supply continuity for manufacturing activities.
Manage purchase orders in SAP, including creation, follow-up, and invoice validation.
Monitor stock levels and identify risks of shortages, taking proactive actions.
Collaborate with quality and production teams to ensure timely material release aligned with production needs.
Maintain accurate master data and supplier information.
Contribute to continuous improvement initiatives and support operational excellence.

Interested? For this role we’re looking for the following education, experience and skills

Bachelor’s degree in supply chain, logistics, or a related field.
Experience in a regulated manufacturing environment (such as biopharma or similar).
Experience in operational procurement or material planning.
Strong organizational and communication skills, with the ability to work cross-functionally.
Proficiency in SAP, Excel, and Microsoft Office tools.
Fluent in French and English.

#genetherapy

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Internal Gene Therapy Manufacturing Operations Quality Partner (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

To strengthen our External and Clinical Supply Quality department, we are looking for a talented profile to fill the position of: Internal Gene Therapy Manufacturing Operations Quality Partner – Braine l’Alleud, Belgium.

About the role
As a key member of the Internal Gene Therapy (GT) Operations Quality team, you will be reporting to the Head of Internal Gene Therapy Manufacturing Operations Quality. You will be responsible for overseeing Drug Substance (DS) development and manufacturing activities within the Gene Therapy Pilot Plant (T4). The position drives continuous QA improvement by ensuring that the Quality Management System and all CMC‑related development activities operate efficiently, consistently deliver high product quality, safety, efficacy and fully meet regulatory expectations.

In addition, the role ensures that all operational and quality activities remain compliant with applicable regulations while supporting strong overall business performance.

You will work with
In this role, you will collaborate closely with the Clinical Manufacturing team, as well as CMC Development, QC, Engineering and Technical Transfer groups to ensure high‑quality Drug Product operations. They will also interact regularly with manufacturing, facility operations, logistics and laboratory teams to resolve deviations, manage changes, and maintain compliance. In addition, the role works in alignment with the broader Internal Gene Therapy Operations Quality team and various stakeholders to support inspection readiness and drive continuous quality improvement.

What you will do

Work closely with Internal Gene Therapy Pilot Plant Clinical Manufacturing Team in charge of the Drug Substance (DS) activities
Ensure quality review of master and executed batch records for drug product supporting clinical trial studies and commercial launch.
Be partner with other departments to identify, mitigate and subsequently resolve compliance and quality issues (Investigations / deviations / out-of-specifications) that may affect UCB development activities and products.
Support Change Control and perform the QA evaluation
Drive the continuous QA improvement process. Ensure adequate documentation processes and systems are available and followed for development projects (SOPs / Protocols / Report review /approval Tech Transfer).
Plan and manage compliance tours and on the floor spot-check of the GMP area, offering quality assurance support including but not limited to inspection

Interested? For this position you’ll need the following education, experience and skills

Bachelor’s/master’s degree or an education in a relevant scientific discipline
Fluent English and French communication (oral and written); any additional languages are a plus.
Extensive experience in pharmaceutical regulated environments, including ATMP and Drug Product manufacturing, isolator technologies and related quality requirements
Deep expertise in Drug Substance, single use technologies and pharmaceutical development processes quality assurance.
Experience managing regulatory inspections (including PAI) and ensuring compliance across manufacturing, facility operations, logistics, laboratory, and quality systems.
Skilled in compliance, quality assurance/control, validation, technical services, and at least one scientific discipline related to pharmaceutical sciences
Understands practical applications of GMP, compliance principles and theories including risk management
Demonstrated autonomy and effectiveness in complex situations, influencing stakeholders and driving results across departments
Excellent interpersonal, verbal and written communication skills at all organizational levels.
Generate commitment from within teams, encourage and support new ideas and act as a role model for others in driving the departmental/company vision.
Develops innovative solutions using sound judgment and extensive quality experience.
Experienced in failure investigations and root cause analysis; coaches others to resolve problems creatively and effectively.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Team Leader Mesure et Instrumentation (pôle biologie) (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Team Leader Mesure & Instrumentation (Pôle Biologique) orienté·e équipe, organisé·e et techniquement solide pour rejoindre notre équipe basée sur notre campus UCB à Braine‑l’Alleud, Wallonie, Belgique.

À propos du rôle

Vous allez encadrer, organiser et coordonner les équipes techniques en charge des activités de contrôle périodique des équipements et des locaux du site UCB Belgium. Vous garantirez la bonne exécution des interventions en thermie et métrologie dans le respect des exigences GxP, qualité et sécurité. Vous assurerez également un rôle de backup technique et organisationnel en l’absence de votre responsable.

Avec qui vous allez collaborer

Vous travaillerez en étroite collaboration avec les équipes BelTech, engineering, maintenance, IT, HSE et production. Vous interagirez avec les sous‑traitants et les utilisateurs internes en tant qu’interface opérationnelle clé. Vous jouerez un rôle central dans la coordination et la communication entre les différents services du site.

Ce que vous allez faire

Vous allez gérer et encadrer les équipes techniques et sous‑traitants en thermie et métrologie
Vous serez responsable de la planification et de l’exécution des contrôles périodiques des équipements (USP, DSP, laboratoires, bioréacteurs, centrifugeuses, BSC,…).
Vous allez superviser les contrôles préventives et curatives des équipements.
Vous veillerez au respect des exigences GxP, qualité, sécurité et environnement.
Vous piloterez la performance au travers de KPI et assurerez l’alignement avec les objectifs du service.
Vous allez rédiger et/ou revoir et/ approuver les documents de contrôle périodique conformément aux Bonnes Pratiques de Fabrication
Vous allez garantir la conformité GMP, HSE et la qualité documentaire.
Vous allez développer les compétences de l’équipe et assurer leur formation continue.
Vous assurerez la gestion des déviations, audits et actions correctives dans les délais.
Vous allez suivre les Actions Correctives et Préventives (CAPAs) et les Changes Controls (CC).
Vous allez participer activement aux audits et inspections réglementaires.
Vous favoriserez un environnement de travail collaboratif et performant.

Intéressé·e ? Pour ce rôle, nous recherchons les compétences et qualifications suivantes

Diplôme de Bachelier en électromécanique ou expérience équivalente.
Expérience en thermie, métrologie ou contrôle technique en environnement réglementé.
Bonne connaissance des exigences GxP, HSE et des systèmes qualité.
Expérience en management d’équipe technique.
Capacité à analyser des processus et à identifier des axes d’amélioration.
Excellentes compétences en communication, assertivité et gestion des parties prenantes.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Local Supply Chain and Warehousing Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

This is a unique opportunity to contribute to one of UCB’s most strategic manufacturing projects and play a key role in shaping the future of biologics manufacturing. We are looking for someone who combines strong operational expertise with the ability to influence complex project decisions, challenge existing thinking, and bring innovative solutions to the table. The ideal candidate is equally comfortable discussing high-level strategic concepts as they are diving into operational details and understands how today’s decisions will impact manufacturing performance for years to come.

About the role:

This role is part of the Manufacturing project, a strategic initiative to build UCB’s next-generation biologics manufacturing facility in Georgia, USA.

As Local Supply Chain & Warehousing Lead, you will represent Internal Manufacturing throughout the design and delivery of the facility, ensuring that supply chain and warehousing requirements are fully integrated into project decisions from concept through implementation. Acting as the voice of operations, you will bring practical expertise, operational insight, and industry best practices to help shape a facility that is efficient, compliant, scalable, and ready to support future manufacturing needs.

Who you’ll work with:

You will be part of the Internal Manufacturing team and work closely with Supply Chain, Manufacturing, Engineering, Quality, Digital, Automation, and Project Delivery teams across UCB.

You will also collaborate with manufacturing sites and global functions to gather operational insights, benchmark best practices, and ensure lessons learned are incorporated into the future facility design. Working across multiple stakeholders, you will act as a key link between project teams and manufacturing operations, helping translate operational needs into effective project solutions.

What you’ll do:

Represent Internal Manufacturing throughout the project, ensuring supply chain and warehousing requirements are embedded into facility design and project decisions.
Define user requirements and translate operational, technical, and business needs into practical, compliant, and future-ready solutions.
Provide subject matter expertise across planning, procurement, warehousing, inventory management, material flows, logistics, and distribution processes.
Collaborate with manufacturing sites and global stakeholders to gather best practices, operational knowledge, and lessons learned from existing operations.
Review technical documentation, process designs, layouts, and operational concepts to ensure they support long-term manufacturing performance and business objectives.
Identify gaps, risks, and improvement opportunities, while actively influencing project teams to develop robust and sustainable solutions.
Contribute to the design of efficient and scalable supply chain and warehousing operations that support both current and future manufacturing requirements.
Monitor industry trends, emerging technologies, and innovative practices to help shape future-ready manufacturing capabilities.
Ensure Quality, GMP, HSE, and compliance requirements are considered and embedded throughout all project phases.
Promote operational excellence and support project decisions that enable safe, reliable, and efficient manufacturing operations from day one.

Interested? For this role, we’re looking for the following education, experience and skills:

Bachelor’s or Master’s degree in Supply Chain, Engineering, Life Sciences, Operations Management, or a related field.
Relevant experience within biopharmaceutical operations and regulated manufacturing environments.
Strong expertise in supply chain and warehousing operations, including planning, procurement, inventory management, storage, logistics, and distribution.
Experience supporting large-scale pharmaceutical or biotechnology projects, facility start-ups, capital projects, or manufacturing transformations.
Strong understanding of the systems, processes, and technologies supporting modern supply chain and warehouse operations.
Ability to translate operational requirements into clear business, technical, and project requirements.
Strong stakeholder management skills with the ability to influence and collaborate effectively across functions and organizational levels.
Ability to balance strategic thinking with operational detail and navigate complex project environments.
Excellent communication and technical writing skills.
Self-motivated, proactive, and solution-oriented, with a strong continuous improvement and innovation mindset.
Ability to work effectively in a rapidly evolving environment with changing priorities and project needs.
Fluent in English, both written and spoken. French is an advantage.
Occasional travel to the United States may be required during the project phases.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

US Bio Manuf. Drug Substance Expert (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Senior Biomanufacturing Process Expert who is collaborative, innovative, and strategic to join our Biomanufacturing Project Team, based in the United States and supporting our future biologics manufacturing site in the Atlanta, Georgia metropolitan area.

About the role

UCB is investing in a new state-of-the-art biologics manufacturing facility in the United States to support our growing number of patients. As a Senior Biomanufacturing Process Expert, you will play a key role in shaping the design and future startup of this high-volume mammalian antibody manufacturing site. You will bring deep technical expertise to ensure manufacturing processes, facility design, and operational strategies align with UCB's biologics pipeline and long-term manufacturing goals.

Who you'll work with

You will work with a highly collaborative and multidisciplinary team spanning Manufacturing, Manufacturing Science and Technology, Development, Engineering, Industrialization, Quality, and project leadership. You will partner closely with engineering design firms, process engineers, and future site users to deliver a facility that supports UCB's future biologics portfolio and operational excellence.

What you'll do

Serve as biomanufacturing process expert for facility design decisions.
Align manufacturing capabilities with future biologics pipeline requirements.
Provide technical guidance on process equipment and facility layouts.
Lead cross-functional reviews and technical decision-making activities.
Author and review technical documentation and operational standards.
Support startup readiness and successful facility implementation.

Interested? For this role we're looking for the following

Minimum requirements

Doctorate with 6+, master's with 10+, or bachelor's with 15+ years' experience.
Experience in biologics development, manufacturing, engineering, or process sciences.
Expertise in mammalian antibody drug substance manufacturing processes.
Experience leading technical decisions within complex cross-functional organizations.
Strong technical writing and document review experience.
Willingness to travel and eventually relocate to Georgia.

Preferred requirements

Expertise in upstream processing, including cell culture and bioreactors.
Expertise in downstream purification and filtration technologies.
Experience supporting large-scale biologics facility design projects.
Knowledge of quality, compliance, and regulatory requirements.
Experience influencing senior stakeholders across global organizations.
Experience supporting greenfield manufacturing facility startups.

This positions reasonably anticipated base salary range is $148,000 - $195,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Communication Specialist, Atlanta, GA (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Medical Communication Specialist who is scientifically curious, customer-focused, and compliance-minded to join us in our Epilepsy & Rare Syndromes US team, based in our Atlanta, GA headquarters.

About the role

As a Medical Communication Specialist, you will provide accurate and timely medical information to healthcare professionals, patients, and internal UCB stakeholders. You will serve as a trusted resource and subject matter expert, responding to medical inquiries, interpreting scientific literature and clinical data, and ensuring responses are balanced, compliant, and aligned with applicable regulations and company policies.

Who you’ll work with

You’ll collaborate with teams across Medical Affairs, Clinical Development, Regulatory Affairs, and Pharmacovigilance to gather information and provide consistent, accurate responses. You’ll also work with internal stakeholders on training, standard response materials, customer support needs, and medical congress activities.

What you’ll do

Deliver accurate medical information to healthcare professionals, patients, and internal stakeholders.
Respond to inquiries using approved resources and compliant documentation practices.
Interpret scientific literature, clinical data, and product information.
Collaborate across Medical Affairs, Clinical Development, Regulatory Affairs, and Pharmacovigilance.
Support medical congress booths, scientific exhibits, and pre-congress training.
Improve medical information resources, processes, and customer experiences.

Interested? For this role we’re looking for the following education, experience and skills

Minimum Qualifications

Degree in pharmacy, life sciences, nursing or related field.
2+ years of experience conducting literature searches and critically evaluating scientific literature.
1+ year of experience using medical information databases, software, and office productivity tools.

Preferred Qualifications

Advanced degree such as PharmD, MD, or PhD.
Strong knowledge of medical terminology, pharmacology, and therapeutic areas, with excellent communication, organizational, and documentation skills.
Experience in neurology or epilepsy.
Product launch experience.
Prior experience in medical information, medical affairs, or a related field.
Ability to work independently and collaboratively.
Occasional overnight travel; up to 10% may be required.

This position's reasonably anticipated base salary range is $108k-$141k per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Key Account Manager / Raleigh NC (Raleigh, North Carolina, US)

Make your mark for patients

We are looking for a Key Account Manager (KAM) in Rare Diseases who is patient-focused, exceeds sales objectives, and has worked in a complex selling environment to join us in our Rare Syndromes ∙ Epilepsy US team, based in Raleigh, NC.

About the role

You will keep the marketing & sales objectives and key performance indicators at the forefront for customer segments in the assigned territory. Act decisively and responsively by prioritizing budget allocation to meet territory objectives. As well as effectively implementing marketing initiatives to achieve sales goals.

Who you’ll work with?

Effectively collaborate with cross-functional partners (medical, reimbursement support, managed market team, and specialty pharmacy, and others) to communicate customer needs help build and deliver appropriate solutions to meet those needs. Partner with advocacy groups to support patient education and disease state awareness in the local community.

What you’ll do

Exceed sales objectives by implementing marketing initiatives by developing and implementing business plans
Maximize impact by leveraging all available data sets and stakeholder input
Seek qualified leads and effectively profile new accounts, refine call planning/routing to optimize schedules
Working knowledge of the local managed care reimbursement
Emphasizes accountability and the highest standard of ethical conduct.

Interested? For this role, we’re looking for the following education, experience, and skills

Minimum qualifications

Bachelor's degree BA/BS
7+ years of Biotechnology/Biopharmaceutical sales experience
Proven, documented track record of delivering consistent sales results
Experience calling on customers at a variety of call points (i.e., academic centers, community-based hospitals and private practice offices) both in person and virtual

Preferred Qualifications:

Promoting products specific to CNS/neuroscience, including epilepsy
New product launch experience
Specialty pharmacy/REMS experience

This positions reasonably anticipated base salary range is $144,000 - $189,000 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Lead Immunology ECE (Prague, Prague, CZ)

Make your mark for patients

We are looking for a Medical Lead Immunology for ECE region (East Central Europe) who demonstrates visionary leadership, empowers teams, and champions patient-centric innovation to join our Medical Affairs Team. The successful candidate will inspire collaboration, drive excellence, and embody integrity, core values that reflect our culture.

This role is based at our UCB offices in Warsaw, Poland or in Prague, Czech Republic.

About the role

As Medical Lead Immunology ECE (East Central Europe), you will provide strategic, scientific, and people leadership for the Immunology medical organization in the East Central Europe Cluster (Poland, Czech Republic, Slovakia, Hungary).

You will be accountable for setting and executing the medical strategy across the region, ensuring alignment with global and regional priorities, and for leading, developing, and inspiring a team of Medical Science Liaisons (MSLs) and Medical Solution Leads.

You will act as a senior medical leader and scientific expert, shaping the value story of UCB’s immunology portfolio and ensuring high-quality scientific exchange with both internal and external stakeholders, always in line with the highest ethical and compliance standards.

Who you’ll work with

You will work with the Head of Medical for the East Central Europe Cluster, regional and global Immunology and Medical Affairs colleagues, and supportive cross-functional partners across commercial, market access, evidence generation, and ecosystem teams. And collaborate with external healthcare experts, advocacy partners, and decision-makers, building trusted scientific dialogue grounded in ethics and compliance.

The Immunology MSLs and Medical Solution Leads in the ECE Cluster report directly to this role.

What you’ll do

Enable regional medical strategic direction aligned with global and European priorities.
Foster development for your team of Medical Science Liaisons and Medical Solution Leads.
Welcome and support medical talent across countries in the cluster.
Subject matter expert in immunology, ensuring strong therapeutic area acumen across the organization
Ensure high-quality field planning, execution, and activity follow-up.
Translate complex evidence and data into clear, patient-relevant insights for stakeholders.
Cultivate compliant collaboration with partners and external healthcare experts.

Interested? For this role we’re looking for the following education, experience and skills

Master or PhD in a scientific discipline; advanced medical or doctoral degree is valued.
Strong Medical Affairs, and leadership experience enabling teams’ growth, coaching, and supportive performance conversations.
Expertise in immunology or a closely related therapeutic area.
Strong understanding of clinical development, study management, and real‑world evidence.
Experience working in cross‑functional, regional, or matrix environments.
Digital literacy and comfort working in evolving medical ecosystems.
Successful experience in shaping strategic medical plans and following through from idea to patient impact.
Fluency in English, Polish and or Czech depending on your location, and travel readiness in the region are valued.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

HS Marketing Manager (Tokyo, Tokyo, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

Job Summary
Geographical scope : Japan
Responsible product : BIMZELX (Dermatology HS and all formulation)
Regulatory responsibilities: Financial outcome and all operation

Major Accountabilities/Responsibilities

LeadとともにBIMZELXに関する統合戦略プランおよび戦術プランを策定・実行する（新規適応およびライフサイクルマネジメントを含む）
グローバルのコマーシャル戦略を、日本市場に適したローカライズされたアクションプランへと落とし込む
グローバルチーム、メディカルチーム、サプライチーム、ファイナンスチーム、セールスチームなど関連部門と連携し、中長期計画（ISP）および戦術プランを実行する
ビジネスパートナーとの交渉を通じ、BIMZELXの患者価値およびインパクトを最大化する
患者価値およびインパクト最大化のためのイノベーションを探求する
市場調査および競合分析、製品ポジショニングを含む戦略的マーケティング活動を実施する
BIMZELX HSに関するすべてのオペレーションをLeadとともに主導・管理する
予算および費用の管理を行う
MRおよびデジタルMR向けのトレーニングプランを策定・実行する

Education & Qualifications

Education Level : Bachelor's Degree
Other Qualifications :製薬でのマーケティング経験3年以上
戦略立案の経験有（中長期Plan/Global Planでなくても翌年の活動方針レベルも可）

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBは、神経および免疫領域に注力するグローバルなバイオ医薬品企業です。世界中で約8,500人の社員が、患者さんからインスピレーションを受け、科学の力で前進しています。

UCBで働く魅力

UCBでは、単に業務をこなすのではなく、価値を創造することを大切にしています。私たちは挑戦を恐れず、協力し合い、革新を追求しながら、患者さんのために成果を出すことを目指しています。
誰もが尊重され、受け入れられ、最善を尽くせる平等な機会がある、思いやりと支援に満ちた文化が根付いています。
私たちは常に「その先」を目指し、患者さん、社員、そして地球に対して人間らしさを大切にした価値を提供しています。
UCBで働くことで、自分自身の成長を実感し、自由にキャリアを築き、可能性を最大限に引き出すことができます。

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

External Manufacturing - Alliance Manager (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

To strengthen our External Manufacturing – Drug Product and Devices department, we are looking for a talented and motivated individual to fill the position of: Alliance Manager based in Braine-L’Alleud, Belgium.

About the role :

You will lead the relationship and daily collaboration with an external manufacturing partner across ongoing and future divestment projects. You will coordinate manufacturing-related activities across supply chain, quality, regulatory, technical, legal, finance, and other partner teams to support business continuity, compliant delivery, and successful transfer activities. You will also oversee planning, risk management, issue resolution, and alignment with contractual commitments.

Who you’ll work with :

You will be working in a team that partners closely with colleagues across external manufacturing, supply chain, quality, regulatory affairs, finance, legal, procurement, and technical functions. You will also work day to day with external manufacturing partner contacts and support governance meetings, action tracking, and decision-making across multiple workstreams. The role includes close alignment with the alliance lead and the broader cross-functional project team.

What you’ll do :

Build and manage integrated project plans covering scope, timelines, milestones, resources, budget, and key dependencies for external manufacturing activities within divestments.
Coordinate manufacturing and transfer activities across internal teams and external partners to support continuity, compliance, and delivery.
Identify project risks and interdependencies early, escalate issues when needed, and support practical mitigation and corrective actions.
Maintain open and consistent communication with internal stakeholders and external partners, including governance meetings, minutes, and action follow-up.
Monitor delivery against contractual commitments, service expectations, pricing terms, and change requests in partnership with legal and procurement teams.
Provide cover for the alliance lead when required to support continuity in communication, decisions, and stakeholder alignment.

Interested ? For this role we’re looking for the following education, experience and skills :

Master’s degree in a technical or scientific field.
Experience in the chemical, pharmaceutical, or biopharmaceutical industry, with significant exposure to cross-functional project delivery.
Strong project management experience, including planning, cost control, timelines, change management, procurement, outsourcing, and contracting.
Experience working with external manufacturing, transfer activities, or related operational programs; transfer management experience is an advantage.
Strong relationship-building skills and the ability to work effectively across internal teams and external partners.
Clear communication skills in French and English, with confidence working across functions and cultures.
Solid technical understanding, good judgment, and a focus on ethical, compliant, and high-quality delivery.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Shift Leader Biomanufacturing - Upstream (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un.e Shift Leader Upstream talentueux.se et motivé.e pour rejoindre notre Belgium Biomanufacturing Operations Center à Braine-L’Alleud, Belgique.

Le rôle s’effectue à 100% sur site et comprend des horaires en shift, du lundi au vendredi (6h>14h et 14h>22h).

Concernant le rôle :

En tant que Shift Leader USP, vous jouez un rôle clé dans le lancement et la réussite des phases du projet afin d’atteindre les objectifs de production. Vous coordonnez les activités de votre équipe, planifiez les tâches et soutenez les technicien.nes de production. Vos responsabilités incluent d’assurer la qualité et le respect des délais de production, d’initier et gérer les notifications HSE (Health, Safety, Environment), qualité et maintenance, et de promouvoir un environnement de travail sûr et de haute qualité. Vous êtes un modèle pour votre équipe, et encouragez un esprit de sécurité et de qualité.

Vous travaillerez avec :

Vous intégrez une équipe d’une quinzaine de personnes composée de 2 Shift Leader USP dans laquelle vous encadrez plusieurs technicien.nes. Vous rapportez au USP Team Leader.

Vos activités :

Réaliser les activités de production selon le planning établi
Accompagner et soutenir les technicien.nes sur le terrain
Contrôler le respect des paramètres du procédé et l’enregistrement des données brutes
Guider, coacher et motiver les technicien.nes de production
Encadrer et former les nouveaux.elles engagé.es
Organiser et coordonner les activités hebdomadaires de l’équipe
Remonter les difficultés et réalisations à la hiérarchie
Animer les réunions de coordination de tier 1 et participer aux réunions de tier 2
Encoder les situations dangereuses ou les « quality event » dans l’outil Source
Participer à la préparation et à la revue des documents de production
Encoder les notifications et maintenances de 1er niveau dans SAP PM
Autoriser les interventions techniques sur les équipements
Communiquer efficacement vers les départements de support
Montrer l’exemple en matière de qualité et de sécurité, et faire respecter les règles GMP (Good Manufacturing Practices)
Proposer et mettre en oeuvre des améliorations continues et des actions correctives

Intéressé.e ? Pour ce poste, vous devez posséder la formation, l’expérience et les compétences suivantes :

Bachelier ou équivalent par expérience
Précédente expérience dans un environnement de production pharmaceutique
Précédente expérience dans les activités upstream est un sérieux atout
Excellentes compétences en leadership avec une précédente expérience en gestion d’équipe
Bonnes aptitudes organisationnelles
Bonnes capacités d’adaptation et de résistance au stress
Engagement envers la qualité et la sécurité
Maitrise du Français avec des notions d’Anglais

#Biomanufacturing

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Peer-to-Peer Marketing Lead Dermatology (Atlanta, Georgia, US)

Make your mark for patients

About the role:

The US iDERM Peer-to-Peer (P2P) Lead is a remote or hybrid role that will hold responsibility for design and delivery of best-in-class HCP education/P2P experience for the Psoriasis (PsO) and Hidradenitis Suppurativa (HS) indications. This includes applying P2P/HCP education capabilities, customer, and TA/Brand insight to design and deliver HCP educational experiences. These educational experiences should educate, engage, and enable HCPs to gain comfort in appropriately prescribing UCB’s Dermatology Biologics Products. The role also entails working cross functionally with internal stakeholders such as Dermatology Marketing, Dermatology Medical Affairs, Dermatology Sales Leadership and the Immunology Ecosystem Partnership Leads to ensure optimal engagement at medical meetings, commercial advisory boards and other related activities which ultimately will help position UCB as a future market leader and true partner within Dermatology delivering on the Patient Value Strategy.

Who you’ll work with:

Share operational insights and knowledge from HCP education efforts to the TA/Brand and HCP Marketers to improve impact.
Cultivates and deepen relationships with PsO and HS communities to understand the appropriate partnerships develop a successful initiative that are meaningful for that specific HCP target.
Partners with the HS and PSO Brand Leads to execute successful insight driven activities that will inform overall Brand strategy (i.e Ad boards, HS Congress attendance).
Partner closely with HCP facing functions and teams to achieve HCP education objectives and deliver an integrated education experience, including across the field.
Partner effectively with the HCP Marketers and the Customer Engagement teams to support HCP Education and field communication and training, activities, as appropriate.

What you will do:

Day to Day development and delivery of HCP educational tactical program efforts that enable the achievement of the overall brand strategy and defined metrics.
Define key performance standards and drive effective and efficient approaches in HCP education delivery.
Own day-to-day Peer to Peer operational & logistics required for effective Project Management of key initiatives (i.e. ANF & Quarterly Planning submissions, Ad board & Congress logistics)
Consistently apply industry best practices and ways of working to deliver leading HCP education.
Develops and maintain a keen understanding of the Dermatology business including customers, brand marketing for both the PSO and HS indications.
Operates at the highest level of UCB compliance and professional standards.

Interested? For this position you’ll need the following education, experience and skills:

Minimum Qualifications:

Minimum 7 years’ experience in dermatology sales, marketing, KOL development and/or other directly related roles.
Overnight travel required. Up to 50% of time.

Preferred Qualifications:

Experience working successfully with commercial and clinical functions.

Proven experience in process building and project management.
Ability to interface and collaborate with a variety of external and internal partners in a highly professional manner, serving as the “face” of the company at key conference and events.
Strong influencing skills with those over whom there is no immediate supervisory capacity to achieve objectives.
Results oriented, attention to accuracy and detail, able to set priorities, take appropriate risks in a compliant manner.
Ability to interface with key customers, accounts, physicians, practitioners, industry contacts, and consultants, accomplish corporate objectives.
Ability to understand marketing terminology, trends and adjust accordingly.
Strong project management skills with the ability to manage multiple high priorities and evaluate results making go/no-go decisions.
Excellent interpersonal, oral, and written communication skills. Highly skilled in presenting in front of groups.

This positions reasonably anticipated base salary range is $164,000 to $215,000 per year. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Local Supply Chain and Warehousing Lead (Atlanta, Georgia, US)

Make your mark for patients

UCB is embarking on one of the most significant investments in its history through the development of a new state-of-the-art biologics manufacturing campus in Georgia, USA.

Designed to power the future of biologics, this new facility will strengthen UCB's global manufacturing network, expand supply capabilities for future medicines, and support our long-term ambition of bringing innovative treatments to patients around the world. The project combines cutting-edge technology, sustainability, digital innovation, and operational excellence to create a future-ready manufacturing ecosystem.

As a true greenfield initiative, it offers a unique opportunity to help design, build, and launch a world-class biologics manufacturing facility from the ground up while working within a diverse international team spanning the United States and Europe.

We are looking for talented, curious and ambitious individuals who want to make a lasting impact and contribute to shaping the future of biologics manufacturing at UCB.

We are looking for a Local Supply Chain & Warehousing Lead who is collaborative, proactive, and forward-thinking to join our Internal Manufacturing team, based at our UCB campus in Atlanta, Giorgia.

This is a unique opportunity to contribute to one of UCB’s most strategic manufacturing projects and play a key role in shaping the future of biologics manufacturing. We are looking for someone who combines strong operational expertise with the ability to influence complex project decisions, challenge existing thinking, and bring innovative solutions to the table. The ideal candidate is equally comfortable discussing high-level strategic concepts as they are diving into operational details and understands how today’s decisions will impact manufacturing performance for years to come.

About the role:

This role is part of the Manufacturing project, a strategic initiative to build UCB’s next-generation biologics manufacturing facility in Georgia, USA.

Who you’ll work with:

You will be part of the Internal Manufacturing team and work closely with Supply Chain, Manufacturing, Engineering, Quality, Digital, Automation, and Project Delivery teams across UCB.

What you’ll do:

Represent Internal Manufacturing throughout the project, ensuring supply chain and warehousing requirements are embedded into facility design and project decisions.
Define user requirements and translate operational, technical, and business needs into practical, compliant, and future-ready solutions.
Provide subject matter expertise across planning, procurement, warehousing, inventory management, material flows, logistics, and distribution processes.
Collaborate with manufacturing sites and global stakeholders to gather best practices, operational knowledge, and lessons learned from existing operations.
Review technical documentation, process designs, layouts, and operational concepts to ensure they support long-term manufacturing performance and business objectives.
Identify gaps, risks, and improvement opportunities, while actively influencing project teams to develop robust and sustainable solutions.
Contribute to the design of efficient and scalable supply chain and warehousing operations that support both current and future manufacturing requirements.
Monitor industry trends, emerging technologies, and innovative practices to help shape future-ready manufacturing capabilities.
Ensure Quality, GMP, HSE, and compliance requirements are considered and embedded throughout all project phases.
Promote operational excellence and support project decisions that enable safe, reliable, and efficient manufacturing operations from day one.

Interested? For this role, we’re looking for the following education, experience and skills:

Mandatory skills:

Bachelor’s or Master’s degree in Supply Chain, Engineering, Life Sciences, Operations Management, or a related field.
+10 years of Relevant experience within biopharmaceutical operations and regulated manufacturing environments.
+6 years of experience supporting large-scale pharmaceutical or biotechnology projects, facility start-ups, capital projects, or manufacturing transformations.
Strong expertise in supply chain and warehousing operations, including planning, procurement, inventory management, storage, logistics, and distribution.
Strong understanding of the systems, processes, and technologies supporting modern supply chain and warehouse operations.
Ability to translate operational requirements into clear business, technical, and project requirements.
Ability to balance strategic thinking with operational detail and navigate complex project environments.
Excellent communication and technical writing skills.
Self-motivated, proactive, and solution-oriented, with a strong continuous improvement and innovation mindset.
Ability to work effectively in a rapidly evolving environment with changing priorities and project needs.
Regular travel to Belgium and Switzerland may be required during conceptual design and basic design phases.

Strong advantages:

Ability to communicate in French.

The reasonably anticipated salary range for this position is $ 148,000-194,300 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Principal Computational Methodologist (Belgium) (Anderlecht, Brussels, BE)

Make your mark for patients

We are looking for a Principal Computational Methodologist who is curious, collaborative, and impact-driven to join our Advanced Methods and Data Science team within Biometrics and Data Science, based in any of our Brussels (Belgium), Slough (UK) or Raleigh (US).

About the role

You will help shape how advanced AI, machine learning, and computational methods support clinical development. You will design, validate, and deploy models that help teams make evidence-based decisions in areas such as biomarker discovery, clinical trial design, operational efficiency, and patient experience. You will guide scientific thinking, turn complex methods into practical solutions, and help build scalable tools that meet scientific, technical, and regulatory expectations.

Who you will work with

You will join Advanced Methods and Data Science, part of Biometrics and Data Science within Patient Evidence. You will work with clinical, statistical, molecular, operational, engineering, IT, governance, and compliance colleagues across countries. You will also connect with academic, technology, and industry partners. Together, you will explore new methods, share scientific learning, and support teams that use data to improve decision-making across the drug development value chain.

What you will do

You will lead AI and machine learning projects that address clinical development, biomarker, operational, and decision-support needs.
You will design, build, test, and refine modern deep learning models for text, graphs, biological sequences, and clinical data.
You will develop generative AI applications using foundation models, pre-trained models, and large language models.
You will run rigorous, reproducible AI experiments on internal and public datasets to generate publishable scientific results.
You will partner with engineering teams to package methods into applications, platforms, and scalable validated solutions.
You will mentor colleagues, share knowledge, and represent the team through publications, presentations, and external collaborations.

Interested? For this role, we are looking for the following education, experience, and skills:

You have a PhD in Statistics, Computer Science, Engineering, Computational Biology, Statistical Genetics, Mathematics, or a related scientific field.
You bring experience in industry, ideally within pharma, clinical development, life sciences, or another regulated data-focused environment.
You can program confidently in Python, R, or similar languages, and you can support others with practical coding guidance.
You understand supervised, unsupervised, Bayesian, and deep learning methods, and can apply them to real-world scientific questions.
You have experience with ML infrastructure, reproducible research, Linux or HPC environments, and software or platform development.
You communicate clearly with scientific, technical, medical, and business partners, and enjoy working in a collaborative, multidisciplinary team.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

AI Product Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for an AI Product Lead who is strategic, results-driven, and collaborative to join our Patient Supply Digital Transformation team, based at our UCB campus located in Braine-l’Alleud, Belgium.

About the role

In this role, you will be at the intersection of AI, product leadership, and biopharma operations. You will help bring practical AI solutions into the processes that support how UCB manufactures and supplies medicines, with a strong focus on business value, user adoption, and measurable impact. This is a role for someone who can connect complex operational needs with the possibilities of AI, while making sure solutions are trusted, scalable, and fit for use in a regulated environment.

Who you will work with:

As a member of the Digital Innovation team, you will connect and align multidisciplinary AI product delivery squads, working with talented colleagues such as:

Process development, manufacturing and supply experts who bring operational context, priorities, and adoption needs.
Data & technology partners who help design, build, integrate, and scale AI products.
Quality, validation, and compliance experts who help ensure solutions are fit for use in a regulated biopharma environment.

What you will do:

Define the direction and roadmap for AI products that support transformation priorities across process development, manufacturing, and supply.
Make product decisions that balance business value, user needs, technical feasibility, scalability, and fitness for use in a regulated environment.
Work with data and technology teams to move AI products from early exploration to deployment, adoption, and continuous improvement.
Coordinate across multidisciplinary teams to keep priorities, dependencies, decisions, and delivery progress clear.
Drive adoption and measurable impact by embedding AI products into ways of working and monitoring performance over time.

Interested? For this role, we are looking for the following education, experience, and skills:

You hold a Master’s degree or equivalent experience in AI, engineering, computer science, or a related field.
You bring practical experience shaping and delivering AI (incl. generative and agentic AI) products, with a practical understanding of what it takes to move from idea to adoption.
You have proven experience leading products or digital solutions end to end, including discovery, roadmap definition, MVP delivery, scale-up, adoption, and continuous improvement.
You can connect business priorities with user needs, data realities, technical feasibility, and quality expectations to make sound product decisions.
You communicate clearly with both technical and non-technical audiences and can align stakeholders around outcomes, trade-offs, risks, and delivery priorities.
You are comfortable working in regulated, quality-focused environments, ideally in biopharma, life sciences, process development, manufacturing, supply, or related operational settings.
You bring a collaborative mindset, strong ownership, and the ability to create structure in ambiguity while helping teams deliver practical, responsible AI products.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Digital Marketing Lead ECE (Warsaw, Warsaw, PL)

Make your mark for patients

We are looking for a Digital Marketing Lead East Central Europe who is eager to join our Patient Impact Mid-Market department, based in our site in Warsaw, Poland.

About the role

As a Digital Marketing Lead East Central Europe (ECE), you will drive omnichannel campaigns based on the strategic imperatives of the country’s brand and marketing plans across therapeutic areas (TAs). You will work closely with local marketing and brand manager roles and support the local medical and market access teams.

Your main objective is to drive and implement multichannel and omnichannel engagement with stakeholders based on the brand plans (ISP) in the local market.

Who you’ll work with

You will collaborate cross-functionally to ensure alignment, execution, and implementation of digital initiatives that enhance patient value and stakeholder engagement, especially for healthcare professionals (HCPs).

This role works closely with the Mid Market digital business excellence partner and global omnichannel teams to implement and localize marketing campaigns based on local needs and strategy.

Building and maintaining strong relationships with local marketing and media agencies is crucial.

What you’ll do

Implement and localize centrally developed EU omnichannel campaigns in line with local ecosystem insights, requirements, drivers, local regulations, and brand plan strategic imperatives (ISP).
Build, implement, and manage local digital omnichannel solutions (projects & activities) in the ECE Cluster, from KPI and success definition to performance and ROI monitoring.
Align and discuss local ECE Cluster digital initiatives, issues, and solutions with the Digital Business Excellence Partner Mid Markets to ensure a coherent digital business transformation.
Collaborate with IBM, digital factory, and other internal stakeholders in regular grooming sessions to enable development and/or implementation of locally created digital material.
Analyse and track outcomes of omnichannel campaigns together with marketing brand teams and appropriate stakeholders to ensure ROI and warrant success of campaign KPIs, benchmarking with previous activities.
Leverage digital channels such as social media, CRM systems, websites, and digital education platforms to drive engagement and create unique customer journeys for HCPs and patients.
Align omnichannel patient-focused solutions across the cluster markets and ensure integration of Patient Support Programs, UCBCares, and HCP Portals.

Interested? For this role we’re looking for the following education, experience and skills

Bachelor’s degree in business, digital marketing, digital communication, or life sciences (master’s preferred).
3-4 years of relevant experience in a digital marketing environment.
Experience working within multidisciplinary, cross-functional teams.
Experience within Pharma is highly recommended.
Content creation skills/Photoshop, product launch, SCRUM/agile, and change management experience are a plus.
Strong comprehension of digital communication tools (e.g., programmatic advertising, website CMS, SFMC, Drupal, webinar tools).
Ability to develop and maintain internal and external networks.
Understanding of compliance and regulatory guidelines.
Ability to explain complex digital activities to less digitally savvy colleagues.
Capability to develop and execute omnichannel campaigns aligned with brand strategy.
Strong business planning, marketing campaign, and tactical execution skills.
Ability to brief creative marketing agencies with a focus on ROI.
Analytical skills to translate digital marketing data into business objectives.
Ability to manage multiple media outlets and campaigns.
Excellent written and verbal communication skills.
Fluent in English, Polish and another East Central European language will be a plus.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Team Leader CAD (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Team Leader CAD (computer aided design) qui est rigoureux·se, organisé·e et orienté·e amélioration continue pour rejoindre notre équipe Belgium Support Services & Braine Campus, basée sur notre campus UCB situé à Braine-l’Alleud, Brabant Wallon.

À propos du rôle

Dans ce rôle, vous allez piloter l’équipe CAD et garantir l’exactitude, la disponibilité et la conformité des plans techniques tout au long de leur cycle de vie. Vous allez coordonner les parties prenantes internes, maintenir des standards de qualité élevés et contribuer à l’amélioration continue des processus et outils. Vous jouerez un rôle clé pour assurer une documentation technique fiable au service des opérations sur les sites belges.

Avec qui vous allez travailler

Vous allez travailler au quotidien avec une équipe CAD dédiée et collaborer étroitement avec plusieurs départements tels que la maintenance, l’ingénierie et les opérations. Vous allez agir comme référent·e technique et assurer l’alignement entre les équipes en fournissant des plans techniques précis et à jour.

Ce que vous allez faire

Vous allez encadrer et développer l’équipe CAD en assurant les priorités, la répartition des tâches et la montée en compétences
Vous serez responsable de la gestion complète du cycle de vie des plans techniques
Vous allez garantir la conformité et la qualité des plans selon les normes internes et réglementaires
Vous allez collaborer avec les équipes transverses pour aligner les plans sur les besoins opérationnels
Vous allez améliorer en continu les outils, processus et indicateurs de performance CAD
Vous allez assurer une gestion structurée, accessible et à jour de la documentation technique

Intéressé·e ?

Pour ce rôle, nous recherchons les qualifications, expériences et compétences suivantes :

Vous êtes titulaire d’un Bachelor ou Master dans un domaine technique pertinent
Vous avez une excellente maîtrise des logiciels CAD et des outils de gestion documentaire (Bentley, autocad, BIM, maquettes 3 D, virtualisation, plan architecture, unifilaire, PID, …)
Vous avez une bonne connaissance des normes techniques et des processus de maintenance industrielle
Vous êtes à l’aise avec SAP-PM et les outils bureautiques (Excel, Word, PowerPoint)
Vous avez démontré votre capacité à encadrer, coacher et développer une équipe
Vous faites preuve d’analyse, d’organisation et d’excellentes compétences en communication

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Warehouse & Logistics Lead - Biomanufacturing (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a talented and motivated Warehouse & Logistics Lead to join our Belgium Biomanufacturing Operations Center in Braine-L’Alleud, Belgium.

Here, you will have the opportunity to truly expand your expertise in a dynamic and forward-looking environment where your growth and development are a priority. By working with the latest technologies and innovative techniques, you will help produce groundbreaking medicines that make a real difference for patients – today and in the future.

About the role :

You will oversee warehouse and logistics operations that support biopharmaceutical manufacturing activities. You will be responsible for ensuring materials are stored, managed and supplied efficiently while maintaining the highest standards of quality, compliance and safety. You will also lead a team of logistics professionals, helping them succeed while driving continuous improvement across warehouse operations.

Who you’ll work with :

You will be working in a team that plays a critical role in ensuring manufacturing operations run smoothly and efficiently. Working closely with manufacturing, quality, technical and supply chain teams, you will help deliver reliable logistics services while supporting a culture of collaboration, continuous improvement and operational excellence.

What you’ll do :

Lead daily warehouse operations including receiving, storage, dispensing, internal deliveries and returns management.
Ensure materials are available to manufacturing teams on time and according to operational priorities.
Maintain compliance with quality, safety and regulatory requirement across all logistics activities.
Manage inventory accuracy and optimize warehouse space, storage capacity and material flow.
Lead, develop and support a team of logistics professionals through coaching, training and performance development.
Drive continuous improvement initiatives and support investigations, audits and operational problem resolution.

Interested ? For this role we’re looking for the following education, experience and skills :

Bachelor’s or Master’s degree in Supply Chain, Logistics, Operations Management or a related field.
Experience in leading warehouse, logistics or supply chain operations within a regulated environment.
Strong knowledge of Good Manufacturing Practices, Good Distribution Practices, and warehouse / supply chain management processes.
Experience using enterprise resource planning systems (SAP preferred) and inventory management tools.
Strong communication, problem-solving and cross functional collaboration skills.
Fluent in French and English.

#Biomanufacturing

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

VIE_Support aux opérations externes (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Le site de Braine-l’Alleud est spécialisé dans la synthèse chimique, le développement, la fabrication et le conditionnement de produits pharmaceutiques.

Pour plus d’information : www.ucb.com

Votre mission consistera à supporter les opérations externes d'UCB transversalement (principe actif et formulation).

Collecter et consolider des données auprès de différents stakeholders
Réaliser des analyses de données afin d’évaluer la performance et l’efficacité des opérations
Fournir des feedbacks et recommandations en vue d’améliorer les processus
Contribuer à la mise en place et au suivi de reportings et indicateurs clés
Participer à la définition et à l’amélioration de processus opérationnels
Supporter un programme stratégique en cours et sa structuration
Contribuer à la digitalisation des activités, avec une perspective d’automatisation et d’utilisation de l’IA à moyen/long terme

Votre profil :

Niveau Master
Français et anglais professionnels requis
Capacité à gérer plusieurs activités en parallèle et à prioriser
Bon esprit d’équipe et aisance dans un environnement transverse
Appétence pour la data et les outils IT (bonnes connaissances ou fort intérêt)

Merci de bien vouloir noter que les conditions strictes d’éligibilité à ce programme sont les suivantes :

Avoir entre 18 et 28 ans;
Détenir la nationalité d’un pays membre de l’Espace Economique Européen;
Ne pas avoir travaillé ou vécu dans le pays où aura lieu la mission;
Etre disponible pour se consacrer à la mission à temps plein;
Si vous êtes de nationalité ou de double nationalité française, être en règle vis à vis des obligations de service national de la France (Numéro Identifiant Défense);
Avoir un casier judiciaire vierge.

Si vous ne remplissez pas l'ensemble de ces conditions, nous ne pourrons pas tenir compte de votre candidature.

Account Executive / Harrisburg (Scranton, Pennsylvania, US)

Make your mark for patients

To strengthen and support our up-and-coming launches within US Rare Disease Organization (RDO), we are seeking an Account Executive - Neuromuscular (AE) for our Harrisburg PA territory. The AE is an expert on the practices, delivery networks, and patient populations within their territory.

They will represent UCB in the communities we serve as we strive toward transforming the lives of those living with Rare Diseases. Playing an integral role in identifying and building collaborative relationships with physicians and clinics, the AE embraces and executes marketing and sales strategies. They will master brand messaging, targeting, and digital technology to deliver persuasive, high-impact customer experiences tailored to distinct user segments while maintaining the highest ethical standards.

Major Accountabilities

Consistently exceed territory sales objectives while operating with the highest level of ethics and integrity
Advocate for Rare Disease patients and serve as the authority on the various tools and resources UCB offers to support physicians, pharmacists, and other health care providers.
Create and execute strategic business plans reflecting a thorough understanding of the local market conditions.
Master targeted disease states which include a deep understanding of patient journeys, standards of care and treatment drivers.
Continuously expand expertise of all treating and referring physicians, as well as payers, hospital systems, pharmacies, labs, and other components of the care continuum; maintain awareness and remain attentive to the dynamics between different stakeholders that influence patient treatment decisions.
Maintain strong relationships within the payer landscape to ensure providers are informed on coverage and reimbursement status; collaborate with the payer access team to ensure all relevant stakeholders are working with the most-up-to-date information to maximize access and affordability for patients using UCB products.
Foster strong relationships with patient advocacy groups and partner to support appropriate patient education and disease state awareness activities in the community.

Interested? For this position, you’ll need the following education, experience, and skills:

Bachelor’s Degree.
8+ years of field-based specialty pharmaceutical experience in sales, account management, and/or field reimbursement in biopharmaceuticals or healthcare, inclusive of 5+ years in a competitive specialty market segment.
Field experience with Buy-and-Bill medical benefits, Specialty Pharmacy, and HUB delivery models.
Verifiable record of sustained high sales performance
Experience with successful product launches.
Comfortable spending up to 40% of time traveling with overnight travel required or based individual territory requirements.

Preferred Experience

2+ years rare/orphan drug experience in competitive market.
Significant CNS/neuroscience sales experience (to include epilepsy); Oncology, Hematology and/or Specialty reimbursement products requiring Specialty Pharmacy knowledge and expertise.
Participation in recent successful product launches.
Experience in supporting biologic therapy administered by a designated health care provider.
Promotional product experience with REMS requirements.

Note: This position's reasonably anticipated salary range is $150,000-$170,000 annually. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

EU Regulatory Science Lead (Anderlecht, Brussels, BE)

Make your mark for patients

We are looking for an EU Regulatory Science Lead who is strategic, collaborative and adaptable to join our Global Regulatory Affairs team, based in our Brussels, Belgium offices.

About the role

You will drive the EU regulatory strategy and activities for assigned products across development, approval and lifecycle activities. You will be the main regulatory contact for EU health authority interactions, including the EMA where relevant. You will help shape practical plans, identify regulatory risks, and work with global and regional partners to support timely submissions and informed decision-making.

Who you will work with

You will work closely with the Global Regulatory Lead, EU affiliates, Global Regulatory Affairs colleagues, submission teams, and cross-functional partners across development, clinical, medical, safety, quality and commercial teams. You will also collaborate with EU health authorities and contribute regional insight into global regulatory planning.

What you will do

You will develop and implement EU regulatory strategies aligned with business objectives and global regulatory plans.

You will be responsible for coordinating EU submission activities in line with regulations, guidelines, timelines and agreed strategies.

You will manage EU regulatory risks by identifying options, recommending practical actions and supporting mitigation plans.

You will act as the key EU contact for assigned products, including EMA and national agency interactions where needed.

You will communicate clear regulatory plans, risks and updates to leadership, affiliates and cross-functional stakeholders.

You will maintain awareness of evolving EU regulations, guidelines, competitor activity and potential impact on product plans.

Interested? For this role, we are looking for the following education, experience, and skills:

You have a degree in life sciences, pharmacy, medicine, law or another relevant scientific or regulatory field.

You bring strong experience in EU regulatory affairs, including product development, marketing authorisations and lifecycle management.

You understand EU regulatory frameworks, procedures, health authority expectations and the evolving policy environment.

You can translate complex regulatory information into clear recommendations for different audiences.

You work well across functions, cultures and organisational boundaries, building alignment through evidence and credibility.

You are curious and aware about digital tools, data science and AI, and their potential impact on regulatory science.

You can adjust to changing conditions, learn quickly, and remain effective in evolving regulatory and scientific landscapes.

You are self-aware and looking for continuous learning and growth of self and others, by seeking and giving constructive feedback.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Material Planner (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Material Planner qui est organisé·e, orienté·e solutions et collaboratif·ve pour rejoindre notre équipe au sein du département de Clinical Manufacturing, basée sur le site de Braine-l’Alleud, Belgique.

À propos du poste

Vous travaillerez au sein d’une équipe qui assure l’approvisionnement en matières nécessaires aux activités de production. Vous coordonnerez la planification des besoins, les commandes et la gestion des stocks afin de garantir la continuité des opérations tout en limitant les risques et en respectant les exigences réglementaires.

Avec qui vous allez travailler

Vous collaborerez étroitement avec les équipes supply&Logisitcs, qualité, production et avec des fournisseurs externes. Le rôle implique des intéractions quotidiennes avec plusieurs parties prenantes pour garantir la disponibilité des matériaux.

Ce que vous allez faire

Coordonner la planification des matières, du forecast jusqu’à la livraison, afin d’assurer la continuité des activités de production.
Gérer les commandes dans SAP, incluant la création, le suivi et la résolution des litiges liés à la facturation
Suivre les niveaux de stock et anticiper les risques de rupture en proposant des actions adaptées.
Collaborer avec les équipes qualité et production pour assurer la disponibilité des matières.
Maintenir les données de référence fournisseurs et articles à jour.
Contribuer aux initiatives d’amélioration continue et à l’efficacité des processus.

Intéressé·e ? Pour ce poste, nous recherchons le profil suivant

Diplôme de niveau Bachelor en supply chain, domaine équivalent.
Expérience dans un environnement de production réglementé (biopharmaceutique ou similaire).
Expérience en gestion des approvisionnements ou planification de l’approvisionnement des matières.
Excellentes capacités d’organisation et de communication, avec un esprit collaboratif.
Bonne maîtrise de SAP, Excel et des outils Microsoft Office.
Maîtrise du français (fluent or native) et de l’anglais.

#genetherapy

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Rheumatology Clinical Account Specialist-Minnesota South (Minneapolis, Minnesota, US)

Make your mark for patients

To strengthen our Rheumatology Sales Team, we are looking for a talented individual to fill the position of: Rheumatology Clinical Account Specialist – Minnesota South. (Including St. Paul, Bloomington and Rochester)

Candidate can live within the geography, preference is Minneapolis or Rochester MN.

About the role

As a Rheumatology Clinical Account Specialist (CAS) you will be responsible for driving demand for the assigned product, by reinforcing the clinical features of the product and UCB value within an assigned territory; engaging and building relationships with clinical decision makers and office support staff to create the best experiences for patients living with severe immunologic diseases who are treated in the home care setting.

Who you’ll work with

Attain sales goals and objectives by product volume as well as other key accountabilities such as reach/frequency with assigned call plan stakeholders
Develops a strong understanding and awareness of the patient journey of care, including the unique needs of patients within the at-home care setting.
Work within the prioritized customer call plan to establish professional working relationships with HCP and support staff.
Offer an outstanding patient experience with our product by communicating clinical information on assigned UCB product and relevant patient support services

What you’ll do

Establishing an understanding of the local ecosystems, including the payor environment, including pharmacy benefits; demonstrating the ability to successfully navigate the complexities of local care delivery systems and models, comprised of multiple payers, with varying degrees of restriction and barriers to patient access for the assigned UCB product.
Maintaining a thorough understanding of the competitive marketplace and drivers of prescriber decisions.
Demonstrating consistent application of the UCB Patient Value Strategy principles by establishing collaborative and team-oriented working relationships, integrating with local UCB ecosystem business partners, in a matrix environment encompassing Field Reimbursement Managers, Immunology Clinical Account Specialist, Partnership Leads, Regional and National Account Executives and Medical Science Liaisons
Knowing when and how to bring in the right expertise at the right time from other UCB matrix roles based on the customer need or opportunity at hand
Conducting account related activities such as profiling, call planning, reviewing UCB sales data, related to at-home administration with assigned stakeholders

Interested? For this role we’re looking for the following
Minimum Qualifications:

Bachelor's degree BA/BS
3 + years direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry
Must have a valid US Driver’s License and with no more than 3 moving violations in the past 2 years
Must reside within assigned territory

Preferred requirements:

Experience selling injectable products
Experience in calling on Rheumatologists
Discussing therapeutic strategies to inform and influence decision makers
Developing and applying clinical and business expertise, and effective selling skills
Executing marketing strategies at the local level
Demonstrated understanding of managed care landscape and how it influences/impacts business

This positions reasonably anticipated base salary range is $132,000-174,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Physical Asset Manager - Infrastructure & HSWB Assets (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Global Physical Asset Manager – Infrastructure & HSWB Assets who is analytical, collaborative, and strategic to join our Global Physical Asset Management / Transversal Asset Fleet Management team, based at our UCB campus located in Braine-l’Alleud, Belgium, or Bulle, Switzerland.

About the role

You will help shape the future of UCB’s infrastructure, underground, and Health, Safety & Well-Being asset landscape at global level. You will define asset strategies that support lifecycle performance, site integrity, workforce protection, operational resilience, regulatory compliance, and long-term business value. You will play a key role in making physical asset decisions more risk-based, data-driven, standardized, maintainable, and aligned with UCB’s growth ambitions.

Who you will work with

You will join the Global Physical Asset Management team and work closely with experts across Business, EHS, Engineering, Facilities Management, QA, Operations, Technical Services, Finance, Procurement, and ISSP. You will collaborate with site and global stakeholders to challenge priorities, align investment decisions, and support practical asset strategies across UCB’s global network.

What you will do

You will co-develop global asset management standards, governance principles, and lifecycle methodologies across infrastructure and HSWB (Health, Safety & Well-Being) assets.
You will lead modernization and renewal strategies using risk-based, data-driven asset insights and prioritization.
You will maintain a consolidated fleet view covering asset condition, compliance, supportability, performance, and investment needs.
You will manage lifecycle strategies for infrastructure, underground assets, and safety-related HSWB systems.
You will ensure asset decisions reflect prevention, protection, compliance, operational safety, and enterprise risk expectations.
You will partner with key functions to build business cases and align investments with enterprise objectives.

Interested? For this role, we are looking for the following education, experience, and skills:

You hold a Master’s degree in engineering, asset management, facilities, or a related technical field.
You bring strong experience in asset management, lifecycle management, and technical risk management.
You understand infrastructure, underground assets, safety systems, lifecycle needs, and degradation mechanisms.
You can build business cases linking asset decisions to resilience, cost competitiveness, COGS, and EBITDA.
You communicate complex technical topics clearly and influence senior stakeholders with practical recommendations.
You are fluent in French and have full professional proficiency in English; IAM certification is a plus.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Team Leader Biomanufacturing - Media Buffer (shift am/pm) (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons plusieurs Team Leaders Biomanufacturing – Media Buffer (semaine shift de jour) talentueux.ses et motivé.es pour rejoindre notre Belgium Biomanufacturing Operations Center à Braine-L’Alleud, Belgique.

Le rôle s’effectue à 100% sur site en horaire en shift, du lundi au vendredi (6h-14h et 14h22h).

Concernant le rôle :

En tant que Team Leader Media Buffer, vous jouerez un rôle clé dans la supervision et l’optimisation des activités de production Buffer & Media. Vous serez responsable de la coordination des opérations, du respect des normes de sécurité et de qualité, et de l’amélioration continue des processus. Ce poste s’inscrit dans un environnement dynamique et collaboratif, où l’accompagnement des équipes et la communication sont essentiels.

Vous travaillerez avec :

Vous travaillerez au quotidien avec une équipe de technicien.ne.s que vous accompagnerez, en collaboration étroite avec les fonctions supports telles que l’assurance qualité, le contrôle qualité, la maintenance et la validation, ainsi qu’avec les nouveaux.elles arrivant.e.s que vous intégrerez et formerez, afin de garantir la continuité, la performance et l’amélioration continue des activités de production.

Vos activités :

Organiser et gérer le planning de production, les horaires et la gestion des installations
Apporter un soutien à l’équipe pour la réalisation des activités de production
Appliquer et faire respecter les règles de sécurité, d’hygiène et de qualité
S’assurer que le personnel est formé et que les équipements sont qualifiés, calibrés et maintenus
Communiquer clairement les informations importantes et signaler les problèmes critiques
Collaborer avec les fonctions supports pour garantir la continuité des opérations
Prendre en charge les actions immédiates en cas de dysfonctionnement ou d’anomalie
Initier et documenter les incidents qualité et EHS (Environment, Health, Safety), et participer aux investigations
Identifier et soutenir des actions d’amélioration continue pour optimiser la production
Participer à l’intégration et à l’accompagnement des nouveaux.elles membres de l’équipe

Intéressé.e ? Pour ce poste, nous recherchons la formation, l’expérience et les compétences suivantes :

Expérience en biotechnologie ou industrie pharmaceutique
Expérience confirmée en management d’équipe
Bonne connaissance des GMP (Good Manufacturing Practice) et des standards qualité
Capacité à faire face à des situations urgentes et prendre des décisions à son niveau
Capacité à travailler dans un environnement dynamique
Excellent esprit d’équipe
Excellentes compétences en Français, niveau intermédiaire en Anglais

#Biomanufacturing

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Reliability Engineer (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Ingénieur·e Fiabilité orienté·e amélioration continue, méthodique et structuré·e pour rejoindre notre équipe basée sur notre campus UCB à Braine‑l’Alleud, Belgique.

À propos du rôle

Vous allez améliorer la fiabilité, la disponibilité et les coûts de maintenance des actifs techniques du site de Braine. Vous garantirez la performance des équipements dans le respect des exigences GMP, HSE et réglementaires. Vous appliquerez les principes d’asset management, les méthodologies de fiabilité et une approche basée sur le risque afin d’optimiser les performances et les décisions techniques.

Avec qui vous allez collaborer

Vous travaillerez en étroite collaboration avec les équipes Maintenance, Production, Engineering, Qualité et HSE. Vous interagirez avec les asset owners et les experts techniques pour soutenir les décisions liées aux performances, aux coûts et aux risques. Vous contribuerez également aux projets, audits et investigations techniques du site.

Ce que vous allez faire

Vous allez définir et améliorer les stratégies de maintenance basées sur la criticité des actifs.
Vous serez responsable de l’analyse des défaillances et de la mise en place de plans d’actions robustes.
Vous contribuerez aux décisions liées au cycle de vie des actifs (remplacement, obsolescence, investissements).
Vous assurerez la conformité aux exigences GMP, HSE et réglementaires et supporterez les audits.
Vous exploiterez les données et contribuerez au développement de la maintenance prédictive.
Vous collaborerez avec les parties prenantes pour optimiser la performance, les coûts et les risques.
Vous suivez les équipes de sous-traitants et vérifiez leur travail.

Intéressé·e ? Pour ce rôle, nous recherchons les compétences et qualifications suivantes

Diplôme d’ingénieur en mécanique, électromécanique ou industriel.
Minimum 5 ans d’expérience en fiabilité, maintenance ou asset management, idéalement dans le secteur pharmaceutique, sur des équipements Pharma/biopharma/clean utilities et équipements de production de froid (jusqu’à -70°). Maîtrise des méthodologies de fiabilité (RCA, FMEA, RCM).
Expérience avec des outils CMMS type SAP PM et analyse de données.
Bonne connaissance des environnements GMP, HSE et réglementés.
Esprit analytique, capacité de résolution de problèmes et forte collaboration transverse

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

VIE_Analyste Environnement & Santé (Environmental & One Health Analyst) (Anderlecht, Brussels, BE)

Faites la différence pour les patients

Le site de Braine-l’Alleud est spécialisé dans la synthèse chimique, le développement, la fabrication et le conditionnement de produits pharmaceutiques.

Pour plus d’information : www.ucb.com

Votre mission consistera à:

Analyser l’impact environnemental des parcours de soins sur différentes aires thérapeutiques (ex : épilepsie)
Réaliser des revues de littérature sur les interactions entre changement climatique, pollution et pathologies ciblées, dans une approche One Health
Appliquer des référentiels et méthodologies du secteur (notamment Sustainable Healthcare Coalition – SHC) à des cas concrets
Identifier les principaux contributeurs à l’empreinte environnementale des parcours patients (hospitalisations, traitements, diagnostics, etc.)
Étendre les analyses à plusieurs pathologies et contribuer à des projets transverses
Participer à la construction de narratives à destination des payeurs et organismes d’évaluation, en valorisant les bénéfices environnementaux
Contribuer à des initiatives visant à rendre les essais cliniques plus durables
Soutenir des programmes européens (ex : PHARMECO) liés à la mesure et à la réduction de l’impact environnemental des médicaments
Présenter les analyses et recommandations aux équipes internes (affaires médicales, accès au marché, sustainability, équipes produit)
Formaliser des méthodologies d’analyse claires, robustes et reproductibles
Développer des supports de formation et de diffusion des bonnes pratiques
Construire des cartographies des parties prenantes et des processus au sein de l’unité « Patient Evidence »
Proposer des pistes d’intégration de l’approche environnementale dans les processus existants
Définir et suivre des indicateurs de performance environnementale (KPIs)
Concevoir des outils de pilotage (ex : dashboards) pour monitorer les progrès dans le temps
Contribuer au développement d’une approche structurée et opérationnelle au service de la stratégie environnementale et d’accès au marché d’UCB

Votre profil :

Diplôme Bac+5 (Master ou diplôme d’ingénieur) dans un domaine scientifique : santé publique, sciences de l’environnement, sciences de la vie ou équivalent
Double compétence environnement & santé fortement appréciée (ex : ingénierie environnementale avec intérêt en santé publique ou inversement)
Maîtrise professionnelle de l’anglais indispensable (langue de travail, littérature scientifique, interactions internationales)
La maîtrise du français constitue un atout, sans être indispensable
Solide rigueur scientifique et capacité d’analyse (revue de littérature, traitement et interprétation de données)
Esprit de synthèse et capacité à structurer des informations complexes
Autonomie, curiosité intellectuelle et proactivité
Bonne maîtrise des outils de la suite Office
Capacité à vulgariser des sujets techniques pour des interlocuteurs non experts
Sensibilité marquée aux enjeux de durabilité et de transition environnementale dans le secteur de la santé
Une première expérience (stage ou alternance) en analyse de cycle de vie (ACV), épidémiologie environnementale ou accès au marché est un plus, sans être obligatoire

Merci de bien vouloir noter que les conditions strictes d’éligibilité à ce programme sont les suivantes :

Avoir entre 18 et 28 ans;
Détenir la nationalité d’un pays membre de l’Espace Economique Européen;
Ne pas avoir travaillé ou vécu dans le pays où aura lieu la mission;
Etre disponible pour se consacrer à la mission à temps plein;
Si vous êtes de nationalité ou de double nationalité française, être en règle vis à vis des obligations de service national de la France (Numéro Identifiant Défense);
Avoir un casier judiciaire vierge.

Si vous ne remplissez pas l'ensemble de ces conditions, nous ne pourrons pas tenir compte de votre candidature.

Contremaître Thermique (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un.e Contremaître Thermique rigoureux.se, organisé.e et orienté.e terrain pour rejoindre notre équipe basée sur notre campus UCB à Braine‑l’Alleud, Wallonie, Belgique.

À propos du rôle

Vous allez jouer un rôle clé de relais opérationnel et technique entre les équipes en assurant la planification, la coordination et l’exécution des activités de vérification des équipements sur le site de Braine. Vous soutiendrez le Team Leader tout en restant actif.ve sur le terrain. Vous garantirez la bonne exécution des activités dans le respect des délais, des coûts et des exigences qualité, sécurité et réglementaires (GMP, GLP, GSP).

Avec qui vous allez collaborer

Vous travaillerez en étroite collaboration avec les équipes techniques, maintenance, engineering, qualification ainsi que les sous‑traitants. Vous serez un point de contact clé entre les utilisateurs et les équipes techniques, en participant aux activités de coordination et de troubleshooting sur le terrain.

Ce que vous allez faire

Vous allez coordonner, planifier et réaliser les activités de vérification, calibrations et ajustements des équipements.
Vous serez responsable de la gestion des plannings à court et moyen terme selon les contraintes opérationnelles.
Vous encadrerez et accompagnerez les équipes techniques et les nouveaux collaborateurs.
Vous apporterez un support technique et participerez activement aux activités de dépannage.
Vous assurerez le respect des normes GMP, qualité et sécurité dans toutes les interventions.
Vous gérerez la documentation, les rapports et les mises à jour dans SAP et Optimu (logiciel de métrologie).

Intéressé.e ?

Pour ce rôle, nous recherchons les compétences et qualifications suivantes

Bachelier en électromécanique ou expérience technique équivalente.
Expérience en environnement technique ou de production, idéalement en industrie réglementée.
Excellente organisation et capacité à prioriser de manière autonome.
Aisance relationnelle avec de multiples parties prenantes.
Flexibilité et capacité d’adaptation à un environnement dynamique.
Connaissances de base en anglais ; expérience SAP et environnement GMP sont des atouts.

Les candidats internes doivent occuper leur poste actuel depuis au moins 12 mois, répondre aux normes de performance et ne pas avoir fait l'objet d'un processus correctif/disciplinaire (PIP), d'un avertissement, d'un avertissement final ou d'une lettre d'avertissement de conformité au cours des 12 derniers mois. Veuillez informer votre responsable ou votre Talent Partner avant de postuler à une offre d'emploi interne.  

Numéro de réquisition du poste (Requisition ID): 93584 

Recruteur (Talent Advisor): Flore Bourlet 

Responsable de l’embauche (Hiring Manager): Sandy Marteleur  

Partenaire RH (Talent Partner): Joelle Coldrick 

Grade: A

System Automation SME (subject matter expert) (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a System Automation SME who is detail-oriented, collaborative, and solution-driven to join our team, based in our Braine-l'Alleud office in Belgium.

About the role

You will play a key role in delivering automation expertise across our manufacturing facilities in Belgium. You’ll ensure quality, compliance, and efficiency in automation deliverables throughout the project lifecycle.

Who you’ll work with

You’ll collaborate closely with automation integrators, production, maintenance, quality, and engineering teams to ensure smooth coordination and optimal outcomes.

What you’ll do

You develop and maintain automation documentation and software.
• You attend workshops and align project disciplines.
• You follow up with automation integrators and vendors.
• You verify deliverables and anticipate cost increases.
• You ensure GMP and HSE compliance.
• You organize operator training and handover to operations.

Interested? For this role, we’re looking for the following education, experience, and skills

Bachelor or Master degree in automation.
• Minimum 5 years’ experience in GMP process automation.
Strong knowledge of PCS7.
• Fluent in French and English.
• Strong design, execution, and validation skills.
• Excellent communication and leadership abilities.
• Risk management and adaptability in dynamic environments.

Be part for 24/7 guard support in hybrid model with Automation Integrators and ready to travel a limited period of time.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Head of China RA (Beijing, Beijing, CN)

Make your mark for patients

Major Accountabilities/Responsibilities：

Define and drive China regulatory strategy for UCB’s candidates and assets, ensuring alignment with global development plans and clear communication of strategic options, risks, and opportunities.
Act as UCB’s China regulatory subject matter expert, maintaining current knowledge of the regulatory environment, shaping policy where possible, and representing UCB in external forums and with key health authority stakeholders.
Lead, develop, and resource a high-performing China regulatory organization that fosters psychological safety, constructive debate, collaboration, and continuous development.
Serve as an active member of the China development team, connecting stakeholders behind a common vision and enabling aligned China development solutions.
Champion change and modern ways of working, including the thoughtful use of technology and AI solutions to accelerate drug development and regulatory approvals.
Build credible internal and external relationships and secure the resources needed to deliver UCB’s China regulatory and development objectives.

Experience:

15+ years in the pharmaceutical industry, including significant regulatory leadership experience in China and a strong track record of regulatory achievements.
Deep understanding of drug development, lifecycle management, and global regulatory requirements, with the ability to connect China and global strategy.
Current knowledge of the China regulatory environment and demonstrated ability to interpret policy, assess impact, and shape the external environment through engagement with authorities and trade associations.
Interest in digital innovation, modern technology, and AI-enabled solutions that can accelerate development and regulatory approvals.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien.ne de maintenance (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

Nous cherchons un.e Technicien.ne de Maintenance qui est proactif.ve, rigoureux.se et orienté.e sécurité pour nous rejoindre sur notre campus UCB situé à Braine-l'Alleud, Belgique.

À propos du rôle

En tant que Technicien.ne de Maintenance, vous allez assurer les interventions de maintenance curative et préventive des équipements. Vous serez responsable de l'exécution des travaux de maintenance selon les ordres de travail et les règles GMP.

Avec qui vous allez travailler

Vous allez collaborer avec une équipe de techniciens et d'opérateurs, ainsi qu'avec le responsable maintenance. Vous serez également en contact avec les responsables des opérations chimiques et les services de métrologie.

Ce que vous allez faire

Vous exécutez les travaux de maintenance individuellement ou en équipe, sur des équipements tels que des vannes, pompes, débit mètres, échangeurs, capteurs, …
Vous avez la charge de la documentation des interventions dans le logbook de l'équipement.
Vous préparez les interventions avec les pièces et accessoires nécessaires.
Vous participez à la rédaction et à l'adaptation des instructions de maintenance.
Vous respectez les règles HSE et participer aux analyses de risques.
Vous contribuez à la mise à jour des dossiers techniques et des plans des équipements.

Intéressé.e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes :

Diplôme technique secondaire supérieur avec expérience en maintenance industrielle ou bachelier en électromécanique.
Proactivité, importance de la sécurité et affinités en informatique.
Connaissance des règles GMP et des procédés industriels.
Capacité à travailler en équipe et à communiquer efficacement.
Connaissance des langues : français et anglais technique.
Disponibilité pour participer aux gardes techniques (1 semaine par mois) et ouvert à l’horaire 6-14/14-22.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Bio Process Equipments SME (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Bio Process Equipment Subject Matter Expert who is innovative, collaborative, and solution-oriented to join our Global Engineering team, based at our UCB campus located in Braine-l’Alleud, Belgium.

About the role

As a Bio Process Equipment Subject Matter Expert, you will play a key role in shaping the future of UCB’s biopharmaceutical manufacturing capabilities. You will provide technical leadership across the entire product lifecycle, from R&D and CMC development to commercial manufacturing. You will influence equipment strategies, support major CAPEX programs, drive innovation, and ensure that bio-process equipment solutions are scalable, compliant, and fit for future business needs.

Who you will work with

You will work closely with Engineering Project Managers, Manufacturing and Operations teams, CMC Development, R&D, Bio Process Development, Quality Assurance, Validation, and Digital Technology teams. You will also collaborate with equipment suppliers and engineering partners worldwide to support strategic projects, technology adoption, and operational excellence across UCB’s manufacturing network.

What you will do

You will provide technical leadership for bio-process equipment across development and manufacturing activities.
You will support global CAPEX projects from feasibility studies through commissioning and start-up.
You will define equipment requirements and ensure robust, scalable, and compliant engineering solutions.
You will drive qualification, validation, and risk assessment activities using quality-by-design principles.
You will manage technical relationships with suppliers and support equipment selection decisions.
You will promote innovation, standardization, and continuous improvement across sites and projects.

Interested? For this role, we are looking for the following education, experience, and skills:

Master’s degree in Biotechnology, Chemical, Mechanical Engineering, or a related scientific discipline.
Significant experience with biopharmaceutical manufacturing equipment and process technologies.
Proven experience delivering engineering and CAPEX projects in regulated environments.
Strong knowledge of GMP, FDA, EMA, qualification, validation, and risk-based approaches.
Ability to influence stakeholders and translate complex technical challenges into pragmatic solutions.
Excellent communication, collaboration, and change leadership skills in multidisciplinary environments.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Artwork & Packaging Strategist Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for an Artwork & Packaging Strategist Lead who is strategic, collaborative, and decisive to join our Devices, Artwork and Packaging team based out of our campus in Braine-l’Alleud, Belgium

About the Role

As a senior expert, you will define and lead the global artwork strategy across the product portfolio, ensuring effective implementation throughout the lifecycle. You’ll guide a team of A&P Strategists, driving daily activities, supporting development, and fostering a culture of collaboration and continuous improvement.

You will oversee strategic planning and execution for artwork implementation, act as the primary contact for Regulatory Affairs, Supply Chain, and Technical Operations, and resolve artwork-related issues. Your responsibilities include ensuring compliance with global and regional regulations, monitoring KPIs, reporting to senior management, and leading process optimization and digital transformation initiatives. You’ll stay ahead of regulatory changes, share insights, and deliver training programs to build team capabilities and promote best practices.

Who You’ll Work With

You will report to the Head of Artwork & Packaging Operations and collaborate with A&P Strategists, A&P Coordination Experts, Regulatory Affairs, Supply Chain, Technical Operations, and senior management across global and regional teams.

What You’ll Do

Lead development and deployment of artwork strategies across product portfolios
Manage and mentor a team of A&P Strategists, promoting excellence and collaboration
Oversee global product portfolio planning and change assessments for timely, compliant execution
Act as senior point of contact for Regulatory Affairs and key stakeholders
Resolve artwork-related deviations, complaints, and change controls, ensuring effective CAPA implementation
Identify and lead process optimization initiatives for artwork and packaging operations
Maintain expert-level knowledge of global and regional regulatory requirements
Develop and deliver training programs to enhance team capabilities and promote best practices
Monitor KPIs, prepare reports for senior management, and ensure governance standards are upheld

Interested? For this role, you’ll need:

Bachelor’s degree in Life Sciences, Regulatory Affairs, Supply Chain, or related field (Master’s or PhD preferred)
Extensive experience in pharmaceutical artwork and packaging strategy
Proven leadership experience in a global or matrixed environment
Strong understanding of regulatory and supply chain processes
Fluent in English; additional languages are an asset

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Process Engineer (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Process Engineer who is collaborative, solution‑oriented, and quality‑driven to join our Sterile Process Engineering team, based at our UCB campus located in Braine‑l’Alleud, Belgium.

About the role
You are going to play a key role in shaping the future of sterile manufacturing at UCB. As a Process Engineer, you will act as the user representative and project leader for digital and non‑digital initiatives impacting the Sterile Manufacturing Plant. You will drive projects from feasibility to deployment, ensure compliance with GMP and data integrity requirements, and support production teams with strong technical and IT expertise.

Who you will work with
You will work closely with a multidisciplinary network including Production, Engineering, Quality, IT and HSE. You are going to collaborate daily with suppliers, internal experts, project teams, and stakeholders across UCB, contributing to a shared vision of operational excellence, compliance, and continuous improvement within a highly matrixed environment.

What you will do

You will lead or support sterile manufacturing projects from feasibility, risk analysis, and execution to operational handover.
You will lead digitalization initiatives impacting sterile manufacturing in Braine.
You will write, review, and approve GMP documentation supporting production, validation, and regulatory submissions.
You will ensure data integrity, cybersecurity compliance, and 21 CFR Part 11 alignment across departmental activities.
You will provide first‑line IT and process support to production teams, investigations, deviations, and CAPA.
You will drive continuous improvement, technology watch, and contribute to a safer, greener manufacturing environment.

Interested?

For this role, we are looking for the following education, experience, and skills:

You hold a Master’s degree in Engineering, Pharmacy, IT, or equivalent relevant experience.
You bring strong knowledge of GMP requirements and sterile manufacturing environments.
You are experienced in project management and cross‑functional coordination.
You have a very good command of both French and English
You can translate operational needs into IT solutions and IT concepts into manufacturing reality.
You are autonomous, rigorous, and comfortable working in a dynamic, matrixed environment.
You demonstrate strong communication skills, a collaborative mindset, and a proactive approach to problem‑solving.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global SME Clean et Black Utilities (Bulle, Gruyere, CH)

Make your mark for patients

We are looking for a Global Clean & Black Utilities Expert, who is eager to join our Engineering & Sites and Facilities department, based in our manufacturing site in Bulle, Switzerland.

About the role

UCB is transforming the way we manage physical assets across all sites worldwide. As part of this transformation, we are looking for a Global Clean & Black Utilities Expert to join our Physical Asset Management organization within Engineering & Sites & Facilities (ESF).

In this global expert role, you will shape UCB’s strategy for clean utilities and selected non-GMP utility and waste systems, ensuring consistency, innovation, compliance, and safety across all CAPEX and lifecycle projects.

You will be the reference for Clean Utilities globally and play a critical role in defining standards, driving innovation, and influencing major engineering programs across Belgium, Switzerland, the US, Japan, and the UK.

Who you’ll work with

The Physical Asset Management / Asset Technical Standards & Expertise Team.
Engineering & Sites & Facilities project leads.
Global network of experts and external partners (e.g., ISPE).
Asset owners, users, and design engineering leads.
EHS, Quality, and manufacturing stakeholders worldwide.

Your expertise will directly contribute to UCB’s global technical excellence and long-term asset strategy.

What you’ll do

Define and develop global technical standards for clean utilities, gas systems, water pretreatment, and waste systems, integrating safety, sustainability, and regulatory requirements.
Lead the global strategy for utility-related systems on all engineering CAPEX projects and contribute expertise during design reviews and technical assessments.
Provide expert guidance to engineering teams, asset owners, and project leads to ensure robust technical solutions aligned with cGxP, EHS, and Good Engineering Practices.
Monitor technological trends and drive innovation in equipment lifecycle management, digitalization, and sustainable engineering solutions.
Build and lead a global network of internal and external experts, fostering knowledge flow and best-practice sharing across UCB.
Support transformation initiatives across UCB sites worldwide and contribute to technical peer reviews, gap assessments, and competency matrix development.
Act as SME for one Safety / Potential Life-Changing Activity topic (e.g., pressurized equipment, chemical storage & handling, LOTO).
Ensure technical oversight and follow-up of projects managed by Engineering & Sites & Facilities.

Interested? For this role we’re looking for the following education, experience and skills

Bachelor’s or master’s degree in engineering, Chemistry, Pharmaceutical Sciences, or a related technical field.
10+ years of experience in utilities, engineering, or technical operations in the pharmaceutical or regulated industry.
Strong technical background in clean utilities, gas systems, and waste systems in cGxP environments.
Deep expertise in clean utilities (WFI, RO, purified water, clean steam, gases) and waste systems (chemical, process, biowaste).
Strong knowledge of engineering standards, cGMP/GLP, ICH, FDA CMC, ISPE/PDA guidance.
Experience with qualification & validation (V-cycle, ASTM E2500).
Ability to interpret and set up P&IDs and Process Flow Diagrams.
Strong communication skills and ability to influence across multiple levels and functions.
Proven leadership and experience working in large, complex, international projects.
Full professional proficiency in English and French.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Dermatology APP Medical Liaison - East (Field Based, Field Based, US)

Make your mark for patients

About the role:

As a Dermatology Advanced Practice Provider (APP) Medical Affairs Liaison, you will serve as a key field-based scientific partner to dermatology NPs and PAs, supporting the launch and lifecycle management of innovative therapies for chronic skin conditions such as psoriasis, hidradenitis suppurativa and atopic dermatitis. This role reports into the Medical Affairs organization, ensuring scientific integrity and alignment with UCB’s mission to create value for patients.

Who you’ll work with:

Partnering with Dermatology MSLs, Medical Outcome Liaisons, and other field teams in regional/local projects.
Conducting peer-to-peer scientific discussions with dermatology APPs
Supporting APPs at national/regional congresses and local society meetings
Gathering and communicating actionable insights from the APP community to inform medical strategy
Collaborating with cross-functional teams to ensure alignment and responsiveness to field needs

What you’ll do:

Contributing to territory-level medical plans and educational initiatives
Upholding UCB’s core values and ethical standards in all interactions
Ensuring compliance with all applicable laws, regulations, and internal policies
Extensive travel (up to 70%) required, including overnights and some weekends.
Delivering medical education aligned with UCB’s dermatology portfolio and pipeline

Interested? For this role we’re looking for the following education, experience and skills:

Minimum Education/Experience Requirements:

Bachelor’s degree plus NP/PA Degree (MSN, PA).
5 years clinical experience as a Nurse Practitioner (NP) or Physician Assistant (PA) in dermatology, rheumatology or gastroenterology.
Minimum of 3 years of prior pharmaceutical industry experience
Ability to travel up to 70%, including occasional weekends for conferences

Preferred Requirements:

• Doctorate degree.

• Familiarity with payer landscapes including Medicare, Medicaid, and commercial plans.

• Strong understanding of psoriasis, hidradenitis suppurativa and atopic dermatitis.

Core Competencies:

Clinical credibility and ability to engage in peer-level dialogue
Strategic thinking and insight generation
Collaborative mindset and ability to work cross-functionally
Strong communication and presentation skills
Commitment to compliance and ethical standards

*This position's reasonably anticipated base salary range is $134,000 - $176,000 annually. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills and experience, among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Device Documentation Specialist (CH) (Bulle, Gruyere, CH)

Make your mark for patients

We are looking for a Device Documentation Specialist who is methodical, detail-oriented, with excellent interrelation skills to join us in our Devices, Artwork and Packaging (DAP) team.

The position can be based in one of our campuses in Braine l’Alleud (BE), or Bulle (CH).

About the Role

This role operates within cross‑functional technical project teams responsible for the design, development, industrialization and life cycle management of drug–device combination products. The Device Documentation Specialist supports device development programs by coordinating documentation activities, tracking key deliverables, and ensuring the integrity, consistency and availability of development data required for design reviews and regulatory submissions.

Who you’ll work with 

Reporting to the Head of Device Transversal Services, you will act as a documentation and project support specialist, partnering with technical teams, project leaders, and regulatory stakeholders to support device and packaging documentation activities. You will help ensure that development documentation and project deliverables remain organized, traceable, and aligned with project timelines and submission requirements.

What You’ll Do

Documentation & Deliverables Coordination :

Support documentation activities across drug-device combination product development programs.

Maintain and track documentation plans and deliverables in alignment with project timelines and key development milestones.

Coordinate the collection, organization and consolidation of technical documentation required for Design Reviews and regulatory submissions.

Monitor documentation readiness and escalate potential delays, gaps or inconsistencies to project teams.

Support the preparation of development and submission documentation packages by ensuring required documents are available and up to date.

Data Integrity & Documentation Quality :

Perform documentation consistency and completeness checks across device and packaging development records.

Support data integrity activities by verifying that documentation is accurate, traceable and aligned across multiple sources.

Assist in identifying documentation gaps, missing information or discrepancies that may impact project deliverables.

Maintain documentation trackers and dashboards to provide visibility on deliverable status and readiness.

Contribute to the implementation of documentation management and data governance best practices.

Cross-Functional Project Support :

Collaborate with technical SMEs, project leaders, quality, regulatory and external partners to coordinate documentation activities.

Organize and facilitate documentation review meetings, follow-up actions and status updates.

Support project teams in planning and tracking documentation-related activities and deliverables.

Provide regular updates on documentation progress, risks and readiness to stakeholders.

Continuous Improvement :

Contribute to the development and maintenance of procedures, guidance documents and working practices related to device documentation activities.

Support initiatives to improve documentation processes, data management and deliverable tracking.

Participate in digitization and process improvement projects related to device and packaging documentation.

Promote consistent documentation practices across development programs.

 Interested? For this role we’re looking for the following education, experience and skills  

Education & Experience :

Bachelor's or Master's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related discipline.

3-7 years of experience in medical devices, drug-device combination products and/or pharmaceuticals.

Experience supporting technical documentation, development projects, regulatory submissions, or quality systems.

Familiarity with design control documentation and regulated product development environments is an advantage.

Knowledge of data integrity and document management principles is desirable.

Understanding of drug‑delivery device regulatory frameworks, including EU MDR, Article 117, GSPR, 21 CFR Part 820, 21 CFR Part 4, ISO 13485, and GMP requirements is an advantage.

Skills & Competencies :

Strong organizational and coordination skills.

Attention to detail and ability to manage multiple deliverables simultaneously.

Ability to track progress and maintain accurate project documentation.

Effective communication and stakeholder-management skills.

Collaborative mindset and ability to work within cross-functional teams.

Proficiency with document management systems and project tracking tools.

Structured and proactive approach to problem solving.

Interest in drug-device combination product development.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Science Liaison, Neurology, Gulf Coast region 1 (Birmingham, Alabama, US)

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UCB is looking for a clinically experienced, science-driven, and patient-focused Medical Science Liaison (MSL) to work on the Epilepsy & Rare Syndromes team for the Gulf Coast geography.

To ensure optimal coverage and engagement within the territory, candidates are ideally based in major hub cities in Memphis, TN, Arkansas, Louisiana, Mississippi, and Alabama.

About the role

The Medical Science Liaison (MSL), Gulf Coast will engage with key scientific and medical influencers to advance understanding of UCB’s Epilepsy and Rare Syndromes portfolio. This role fosters collaborative, science-driven partnerships with key stakeholders to support optimized patient care. The MSL will provide scientific exchange, contribute insights to medical strategies, and drive patient-focused initiatives within the local health ecosystem.

What You’ll Do:

Stay current with research and clinical data related to epilepsy and rare syndromes.

Execute targeted stakeholder engagement strategies to identify local needs and opportunities.
Provide meaningful medical insights to support medical strategies and initiatives.
Represent UCB at scientific conferences and educational events.
Collaborate cross-functionally to enhance patient care and contribute to medical projects as needed.

May lead/support other Medical Affairs projects or activities as assigned.

Who You’ll Work with:

Build and manage trusted, peer-level relationships with Key Opinion Leaders (KOLs), clinical investigators, and patient advocacy groups

Interested? For this role, we’re looking for the following education, experience, and skills

Minimum Requirements:

Doctorate (PhD, PharmD, MD, DPM, or DO) with a minimum of 3 years’ experience as an MSL

NP/PA with a minimum of 3 years’ experience as an MSL or minimum of 3 years of direct clinical experience in relevant therapeutic area or 5 years in the pharmaceutical industry.
Must reside within the assigned territory.

Valid driver’s license and ability to travel 60-80% in the designated territory.

Preferred Qualifications:

Clinical or professional experience in epilepsy and/or rare syndromes.
Strong scientific communication and presentation skills.
Ability to actively listen, identify opportunities, and deliver solutions.
Self-motivated, able to work independently and collaboratively within a cross-functional team.

This role requires 70-80% in-field engagement across the Gulf Coast region

This position's reasonably anticipated salary range is $134k-$204k per year. The actual salary offered will take into account internal equity and also may vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Digital Technology Lead Data Enablement - Master Data (Anderlecht, Brussels, BE)

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We are looking for a DT Lead Data Enablement - Master Data who is strategic, collaborative, and outcome‑focused to join us in our Digital Technology Data Enablement team, based in our HQ in Brussels, Belgium.

About the role

You will shape and steward the enterprise‑wide approach to master and reference data, turning governance strategy into scalable, technology‑enabled capabilities. Working closely with the Data Office, you will define target architectures, guide multi‑year roadmaps, and lead technical delivery across domains. Your work will ensure trusted, secure, and well‑governed data flows reliably across the organization, supporting long‑term value creation and patient impact. This role combines architectural leadership, product thinking, and strong stakeholder partnership at enterprise scale.

Who you’ll work with

You will be working in a team that partners closely with the Data Office, digital delivery teams, enterprise architects, and senior business stakeholders. You will collaborate with internal technology teams and external partners across research, manufacturing, and commercial domains, fostering inclusive collaboration and shared accountability to deliver sustainable, enterprise‑wide data capabilities.

What you’ll do

Define and evolve the enterprise target architecture and long‑term strategy for global master and reference data management
Translate data governance priorities into outcome‑driven technology roadmaps, investment cases, and delivery plans
Lead the technical direction of master data platforms, including data modeling, matching, workflows, and golden record delivery
Design and govern reference architectures, integration patterns, and technical standards aligned with enterprise and cloud strategies
Guide vendor and tooling choices, balancing scalability, security, usability, cost, and long‑term value
Act as trusted advisor, translating complex technical options and trade‑offs into clear, decision‑ready recommendations

Interested? For this role we’re looking for the following education, experience and skills

Master’s degree in computer science, engineering, information systems, or a related field
At least 7 years of experience leading enterprise‑scale master data or data governance technology initiatives
Experience working in GxP evironments would be a strong asset
Strong expertise in data architecture, integration design, and modern data management platforms
Proven ability to translate governance and business strategy into technical solutions and roadmaps
Solid understanding of data privacy, security, and regulatory requirements in regulated environments
Excellent communication and influencing skills with senior technical and business stakeholders

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Value & Access Contracting Lead - Commercial PBM, Payer (Field Based, Field Based, US)

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We are looking for a Value & Access Contracting Lead – Commercial Pharmacy Benefit Manager and Payer to join our Value & Market Access Contracting team located in our Atlanta, GA Headquarters. This position will consider remote candidates (with up to 20% onsite presence).

About the role

The Value and Access Lead is a people leader accountable for leading the multi-channel Market Access & Pricing contracting language strategy and execution, leading a team of 3 Contracting Partners to deliver compliant, timely, and commercially optimized agreements for enterprise-critical books of business.

Who you’ll work with

In a demanding, fast-paced environment, this role serves as the senior cross-functional contracting liaison with Account Management, Analytics, Legal, Finance, Pricing Committee, and Operations—leading high-stakes negotiations and continuously reprioritizing to identify risk, quantify financial impacts, and manage high-value, high-complexity agreements with strong controls, documentation discipline, and a focus on scalable execution and compliance.

What you’ll do

Set multi-channel value & access contracting language strategy across 3 channels (GPOs, Trade, and Specialty Pharmacy); translate brand/access objectives into contracting priorities, negotiation stances, and execution roadmaps.
Own end-to-end contract lifecycle accountability for assigned portfolio(s), including providing inputs and feedback into the Analytics-led modeling deal(s) process, term sheets, and conditions to rebate. In addition, providing negotiation oversight, approvals routing, execution, amendments, and renewals—ensuring timelines, quality, and audit-ready documentation.
Lead and develop a team of 3 Contracting Partners through clear performance expectations, coaching, training and onboarding, workload prioritization, review of work, and capability building; ensure consistent application of negotiating principles, processes, and contract standards.
Manage a high-volume, fast-paced portfolio by continuously triaging and reprioritizing workstreams across channels; align stakeholders on priorities, timelines, and trade-offs; and communicate proactive updates/escalations to ensure timely decisions and execution.
Serve as the senior contracting voice in cross-functional governance with Account Management, Pricing, Finance, Legal, Compliance, and Operations; own the contracting position and recommendation (informed by Analytics-led modeling and approvals) and align on deal economics, access trade-offs, and operational feasibility prior to execution.
Drive contract economics and risk trade-offs by identifying contractual and operational risks, understanding and communicating financial impact/exposure, evaluating financial terms, developing scenario-based recommendations, and escalating decisions that impact P&L, exposure, or channel strategy.
Ensure compliance, controls, and appropriate risk mitigation across all agreements
Oversee operational readiness and issue resolution for executed agreements (implementation requirements, eligibility, adjudication, chargeback/rebate implications); lead timely negotiation and resolution of disputes and contract performance exceptions.
Establish performance management and reporting for the contracting portfolio workflow; communicate clear insights and recommendations to the Head and leadership stakeholders.
Standardize contracting ways of working by implementing templates, playbooks, clause libraries, and training/enablement materials (e.g., onboarding guides, negotiation toolkits) and driving continuous improvement initiatives that reduce variability, improve speed, and increase negotiation leverage.
Represent the function with executive-level presence in internal and external discussions; anticipate channel and payer dynamics, proactively surface risks/opportunities, and influence decisions to protect access, compliance, and enterprise value.

Interested? For this role we’re looking for the following education, experience and skills

Required:

Bachelors Degree
10+ years of experience in Market Access/Value & Access Contracting, Pricing, Reimbursement, Market Access Strategy, Payer/Account Management, or related areas within pharmaceuticals/biotech.
Minimum of (1) 3+ years direct people leadership experience; (2) 1–2 years direct people leadership AND 3+ years leading on cross-functional teams and/or major negotiations with clear accountability for outcomes; (3) 8-10+ years account leadership (deal strategy ownership, governance leadership, delivery against timelines and financial targets); OR (4) 8-10+ years of experience in market access/trade contract redlining and negotiations.

Preferred:

Demonstrated experience developing and delivering training and onboarding for contracting and/or market access teams (e.g., negotiating principles, contracting SOPs, governance pathways, and contracting tools/templates) to drive consistent execution and compliance.
Demonstrated expertise negotiating, drafting, redlining, and operationalizing complex agreements (e.g., rebates/fees, price protection, admin/service fees, dispute terms) with success balancing access, economics, and risk.
Strong working knowledge and commitment to pricing/contracting governance and compliance requirements, including required approval pathways, documentation standards, peer reviews, and partnering effectively with Legal/Compliance.
Advanced financial and analytical acumen to interpret deal models, identify risks, identify and understand financial impacts/exposure, evaluate scenarios, and make clear recommendations to stakeholders and leadership.
Advanced communication and influencing skills with a track record of aligning cross-functional stakeholders
Experience contracting across multiple US market access channels (e.g., Trade/Distribution, GPO/IDN, Specialty Pharmacy, and/or 340B).
Prior ownership of contracting strategy for a brand launch, major indication expansion, or significant access shift (e.g., formulary wins/losses, channel re-architecture).
Exposure to advanced contracting constructs such as outcomes-based/value-based arrangements, performance guarantees, innovative pull-through programs, and complex dispute/true-up mechanisms.
Experience in specialty and/or rare disease market access dynamics strongly preferred.
Strong understanding of contracting operations and financial flows (rebate processing, chargebacks, fees/admin, eligibility, and audit/dispute management) and ability to partner effectively with internal operations teams.

This positions reasonably anticipated base salary range is $164,000 - $215,300. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of Quality Systems & Continuous Improvement (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Head of Quality Assurance Compliance who is strategic, collaborative, and relentlessly quality-driven to join our Site Quality – QA Compliance team, based at our UCB campus located in Braine-l’Alleud, Walloon Brabant, Belgium.

About the role

You are going to set the pace for regulatory compliance and inspection readiness across our pharmaceutical manufacturing site. You will lead the site Quality Management System governance, strengthen a proactive and risk-based compliance approach, and champion a culture where quality is everyone’s responsibility. You will oversee key compliance processes—audits, deviations, corrective and preventive actions, change control, data integrity, and risk management—so you will help protect patients, products, and reliable supply.

Who you will work with

You will work closely with the Site Quality leadership and partner daily with Manufacturing, Technical Operations, Regulatory Affairs, and global Quality colleagues to keep the site in a sustained state of control. You will also collaborate with quality systems and continuous improvement experts who focus on optimizing quality processes, reinforcing standards, and enabling operational excellence across site activities and supporting services.

What you will do

• You will drive inspection readiness and sustained compliance across manufacturing, testing, and all supporting site services.
• You will lead Quality Management System governance, ensuring robust oversight of deviations, corrective actions, and change control.
• You will coordinate regulatory and customer inspections, including preparation, hosting, and timely, high-quality response packages.
• You will lead internal and external audit strategy, ensuring effective follow-up, risk mitigation, and continuous improvement outcomes.
• You will manage the site data integrity office, define the roadmap, and strengthen oversight for equipment-related data.
• You will build, coach, and inspire a high-performing compliance team and develop a practical learning and training culture.

… Interested?
For this role, we are looking for the following education, experience, and skills:
• You will bring a Master’s degree in Chemistry, Life Sciences, or a closely related scientific discipline.
• You will have 10+ years in a regulated pharmaceutical or life-sciences environment, including 5+ years in Quality Assurance.
• You will demonstrate strong people leadership experience, motivating and developing teams of quality professionals.
• You will show expertise in quality systems governance and internal/external auditing within manufacturing environments.
• You will apply risk analysis and mitigation methods with confidence and sound, fact-based decision making.
• You will communicate fluently in French and English, influencing stakeholders with clarity, diplomacy, and accountability.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Pharmacometrics Team Lead (UK) (Slough, Berkshire, GB)

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We are looking for a Pharmacometrics Lead, who is innovative and agile to strengthen our Quantitative Clinical Pharmacology group, based at our research site in Slough (UK), Monheim (Germany) or Braine (Belgium).

About the role

Bringing experience in the application of pharmacometrics to pediatric drug development, Neurology and Immunology, with the aspiration to lead/manage more junior staff, to contribute to the teams’ development and grow expertise and skills in these areas.

Who you’ll work with

Reporting to the Global Head of Pharmacometrics, you’ll be leading a team of Pharmacometricians, from both a technical and scientific perspective, to ensure state of the art pharmacometrics approaches are applied to optimize drug discovery and development.

Working closely with the QCP Leads assigned to the various projects, to ensure clear integration of the pharmacometrics aspects into the programs.

What you’ll do

Coaching and mentoring junior staff on how to navigate within a project and matrix organization.
Leading and delivering the Pharmacometrics strategy to support development of our assets. extrapolation (where appropriate), dose selection, trial design, PIP development and ongoing evaluation of data as generated.
Performing hands-on population PK/PD, exposure-response modeling and clinical trial simulations on an assigned project.
Developing submission ready fit for purpose Pharmacometrics analysis plans and reports.
Initiating and overseeing outsourced pharmacometrics activities and further internalizing the work as needed.
Having a working knowledge about the regulatory pathways on a global basis and opportunities for collaboration with health authorities (either through working parties, advice meetings, and other initiatives) in pediatrics, Neurology and Immunology.
Promoting MID3 internally and externally.

Interested? For this role you’ll need the following education, experience and skills

Doctorate (PhD or MD) in the related disciplines of Pharmaceutical Sciences, Statistics or Engineering.
8+ years (Bio)pharmaceutical industry experience in Pharmacometrics with minimum of 2 years line management responsibilities.
Hands-on experience in population PK/PD, disease progression modeling, and clinical trial simulations.
Strong understanding and knowledge of Bayesian methodologies, model-based meta-analyses, PBPK, QSP, and AI/ML in Pharmacometrics.
Expertise in R, NONMEM or related pharmacometrics software.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

RIM Operations Systems Manager (Anderlecht, Brussels, BE)

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We are looking for a RIM Operations Systems Manager curious, structured, and people-focused to join us in our Regulatory Community Excellence team, based in our HQ in Brussels (Belgium)

About the role

You will advance our Regulatory Information Management (RIM) systems, supporting their high-impact performance and innovation, with an emphasis on Veeva Vault RIM.

You are going to support RIM system users and turn business needs into system changes, support releases, and make sure our tools stay compliant and easy to use. You will also help bring in smarter ways of working, including automation and AI-enabled features.

Who you’ll work with

You will work with system owners and the RIM Operations team. You will partner with IT, Quality, and stakeholders across the business to improve how regulatory work is supported by data and technology, while driving user adoption and compliance with RIM systems.

What you’ll do

You will support and guide system users by contributing to user guidance and training, managing a shared mailbox, and focusing on change management to help increase adoption and satisfaction.

You will support system ownership activities for the RIM toolset, including Veeva Vault RIM, system integrations, authoring tools, and reporting interfaces

You will coordinate configuration changes, enhancements, testing, and releases to keep the platform stable and fit for purpose.

You will turn operational needs into clear requirements and user stories that teams can build and validate.

You will help improve workflows, prepare user acceptance testing, and confirm changes meet quality and compliance needs.

You will support data and access governance, validation documents, and audit materials to meet GxP expectations.

Interested? For this position you’ll need the following education, experience and skills:

You will bring several years’ experience in Regulatory Operations, RIM, or regulatory systems management in a regulated environment and across global regions.

You will have hands-on experience with Veeva Vault RIM (required).

You will have experience with configuration, releases, testing, and deployments in enterprise systems.

You will understand data integrity and computerized system validation in GxP environments.

You will be experienced working with integrations, vendors, and cross-functional partners to solve issues and improve service levels.

You will be comfortable providing end user support and providing process and system expertise to guide users to compliant use of regulatory systems.

You are knowledgeable about product data submissions (eg, XEVMPD and IDMP) and familiar with global Health Authority submission standards (eg, controlled vocabularies and eCTD)

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Digital Technology Lead Process Excellence & Automation (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Digital Technology Lead Process Excellence & Automation who is strategic, collaborative, and forward-thinking to join us in our Digital Technology team, based in our HQ in Brussels, Belgium.

About the role

In this global role, you will help shape how Digital Technology delivers work more efficiently, consistently, and sustainably across the organization. You will lead the roadmap for process excellence and automation, helping teams improve how platforms and applications are deployed, governed, and supported. You will work across functional and technology teams to turn improvement opportunities into practical, scalable solutions. This role combines leadership, coordination, and innovation, with a strong focus on continuous improvement, modern delivery practices, and long-term value creation in a secure and regulated environment.

Who you’ll work with

You will be working in a team that partners closely with Digital Technology stakeholders, functional leaders, delivery teams, and external partners across multiple regions. You will collaborate with colleagues supporting cloud applications, platforms, cybersecurity and enterprise services, bringing together technical and functional perspectives. The team values curiosity, shared accountability, and practical problem-solving, and works across a diverse stakeholder landscape to deliver reliable, scalable, and future-ready solutions.

What you’ll do

Define and evolve the process excellence and Devops automation roadmap, aligned with Digital Technology strategy, business priorities, and long-term operational goals
Lead the improvement of platform and application deployment practices through automation, standardization, and modern ways of working
Design and support scalable automation and artificial intelligence-enabled solutions that improve efficiency, quality, resilience, and user experience
Coordinate internal and external contributors, ensuring clear priorities, strong collaboration, and consistent delivery across a global scope
Partner with stakeholders to identify improvement opportunities and translate business needs into practical, sustainable, and well-governed solutions
Monitor performance indicators, support budget and resource planning, and drive adoption of new processes, tools, and ways of working

Interested? For this role we’re looking for the following education, experience and skills

Bachelor’s degree in information systems, engineering, computer science, or another relevant field
At least 7 years of experience in process improvement, Devops tooling and processes, automation pipelines, digital transformation, or technology leadership roles within complex organizations
Strong understanding of modern software delivery, platform enablement, automation, and cloud-based technology environments, especially Microsoft platforms (Azure Devops, Github, etc...)
Experience leading cross-functional initiatives and engaging both technical and functional stakeholders across a global environment
Ability to balance innovation, governance, compliance, and risk management in regulated environments
Excellent communication skills, with the ability to explain complex topics clearly and influence decisions at different levels

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of Digital Technology Data and Architecture (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Head of Digital Technology Data and Architecture who is strategic, collaborative and driven to join us in our Digital Technology Manufacturing and Engineering team, based in our Braine l’Alleud office in Belgium.

About the role

You will play a key leadership role in shaping and delivering the digital data and architecture strategy supporting manufacturing, laboratories and patient supply operations. Working in a global and highly regulated environment, you will define standards, guide transformation programs and ensure secure, integrated and high‑quality data solutions. You will balance strategic vision with practical delivery, lead a talented team, and partner closely with business leaders and technology experts to move the organization forward in an increasingly digital and industrial landscape.

Who you’ll work with

You will be working in a diverse, international team of digital technology, data and architecture professionals, closely connected to manufacturing, laboratories, infrastructure and transformation teams. You will collaborate with senior leaders, internal experts and external partners, gaining access to world‑class knowledge while influencing how digital solutions are designed and adopted across patient supply.

What you’ll do

Define, own and communicate the digital data and architecture strategy for manufacturing, laboratories and patient supply, including roadmaps and standards
Lead and prioritise a portfolio of data and technology initiatives, ensuring delivery on time, on budget and aligned with business value
Drive integration, standardisation and simplification of the digital application landscape across patient supply
Act as a trusted partner to stakeholders, translating business needs into scalable, secure and compliant digital solutions
Lead and develop data and architecture professionals, fostering collaboration, innovation and continuous learning
Ensure high levels of data integrity, cybersecurity awareness and compliance within regulated industrial environments

Interested? For this role we’re looking for the following education, experience and skills

Master’s degree in a relevant field such as information systems, engineering or data‑related disciplines
At least 7 years of experience in digital technology roles within global, regulated manufacturing or industrial environments
Strong background in data strategy, application architecture and complex system integration
Experience leading international programs and managing diverse teams and external partners
Ability to influence, navigate ambiguity and bring people on board around a shared digital vision
Strong understanding of manufacturing, laboratory or supply chain processes and data usage

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Projects Automation Lead (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Projects Automation Lead – Engineering who is strategic, collaborative, and delivery‑oriented to join our team based at our UCB campus in Braine‑l’Alleud, Belgium.

About the role

You are going to define and drive UCB’s automation vision across engineering projects and manufacturing sites. You will translate strategic ambitions into a clear multi‑year automation roadmap and ensure its execution through a dedicated automation team. Combining leadership and hands‑on accountability, you will ensure automation solutions are compliant, standardized where needed, and consistently deployed to support long‑term site performance, digitalization, and sustainability.

Who you will work with

You will work closely with engineering project managers, site manufacturing, utilities and facilities teams. You will collaborate with system integrators and suppliers while animating a cross‑site automation network to share best practices, standards, and reusable solutions.

What you will do

You will define and maintain the automation vision, strategy, and multi‑year roadmap for engineering projects and sites.
You will be responsible for building, leading, and developing a central or federated automation team.
You will act as automation discipline owner across capital projects, from concept to handover.
You will ensure automation packages, standards, specifications, and architectures are fit‑for‑purpose and compliant.
You will govern automation initiatives, balancing project delivery with long‑term standardization and sustainability.
You will act as the single point of accountability for automation with internal and external stakeholders.

Interested? For this role, we are looking for the following education, experience, and skills

Master’s degree in Engineering (Automation, Electrical, Industrial, Chemical, or similar).
10+ years of experience in industrial automation within regulated manufacturing environments.
Proven experience leading automation teams or disciplines within capital projects.
Strong understanding of automation systems, validation principles, and project lifecycles.
Ability to translate strategy into execution with a pragmatic, delivery‑focused mindset.

Clear and impactful communication skills, translating complex technical topics for diverse audiences.

Excellent stakeholder management and matrix leadership skills.
Fluent in French and English + willing to travel to UK, Switzerland, Japan (20% of the time).

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Outcomes Liaison, Central (Saint Louis, Missouri, US)

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We are seeking a Medical Outcomes Liaison (MOL), Central to serve as a key scientific partner within our US Medical Affairs Epilepsy and Rare Syndromes team. This field‑based role focuses on building strong relationships with decisionmakers, delivering clinical and economic value, and identifying strategic opportunities that positively impact patients living with Epilepsy and Rare Syndromes. This territory covers AL, AR, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, ND, NE, OH, OK, SD, TN, TX, WI.

Candidates must reside within the territory and live near a hub airport in the territory.

Up to 75% of travel required, including overnights and some weekends.

About the Role

The Medical Outcomes Liaison (MOL) provides clinical insights, Health Economics and Outcomes Research (HEOR) expertise, and real‑world evidence to external stakeholders including integrated delivery networks (IDNs), large medical groups, top‑tier research institutions, and regional payers. You will cultivate high‑value partnerships, assess data gaps, and drive field‑based research collaborations to support strategic medical initiatives.

What You’ll Do

Lead execution of the Epilepsy & Rare Syndromes outcomes and RWE engagement strategy across key accounts.
Build and maintain relationships with C‑suite stakeholders, researchers, and payer decision‑makers.
Identify and develop institutional data opportunities that align with strategic evidence needs.
Support field‑based research collaborations and HEOR data generation.
Serve as an expert communicator delivering clinical and economic value propositions across settings of care.
Partner cross‑functionally to address clinical and HEOR data needs at key accounts.

Who you’ll work with

Senior healthcare leaders, including C‑suite and D‑suite decision‑makers within large medical groups, to support high‑level strategic engagements.
Top‑tier research institutions to advance scientific and outcomes‑focused initiatives.
Pharmacy and medical directors at regional payers, providing clinical and economic insights that inform access and value discussions.
Integrated delivery networks (IDNs) and large medical groups to drive outcomes‑ and RWE‑aligned strategies.
Internal cross‑functional partners—regional business units, marketing, sales, medical affairs, and corporate functions—to ensure coordinated execution across the organization.

Interested? For this role we’re looking for the following education, experience, and skills

Minimum Qualifications

Clinically focused graduate degree (MPH, NP, PA). Doctorate degree (PharmD, MD, DO, PhD, DNP) preferred.
Doctoral candidates: Minimum 8 years industry experience + 3 years HEOR/RWE/Outcomes experience.
Non‑doctoral candidates: Minimum 10 years industry experience + 5 years HEOR/RWE/Outcomes experience.

Preferred Qualifications

Doctorate preferred (PharmD, MD, DO, PhD); non‑doctoral clinicians considered with relevant expertise.
Strong background in external stakeholder engagement and decisionmaker relationship management.
Ability to analyze clinical and HEOR data gaps and deliver meaningful solutions.

This position's reasonably anticipated salary range is $156,000-$238,400 annually. The actual salary offered will consider internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Automation Engineer (Braine L'alleud, Walloon Brabant, BE)

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We are looking for an Automation Engineer who is detail-oriented, collaborative, and solution-driven to join our team, based in our Braine-l'Alleud office in Belgium.

Note that 2 roles are now open : 1 specialized in PCS7 (system engineer) and 1 specialized in PCS7 and Aveva (alarm engineer).

About the role

Who you’ll work with

You’ll collaborate closely with primarily Production, followed by Quality teams (QA and Qualification), and finally IT for compliance with cybersecurity and virtualization regulations in order to ensure smooth coordination and optimal outcomes.

Major projects you could participate in

PCS7: We have 4 infrastructures in Belgium where PCS7 is used,in which there are numerous projects such as the implementation of new molecule production, new equipment, and production optimizations. We also have upgrade projects to keep installations up to date.

What you’ll do

•You attend workshops and align project disciplines.

•You develop and maintain automation documentation and software.
• You follow up with automation integrators and vendors.
• You verify deliverables and anticipate cost increases.
• You ensure GMP and HSE compliance.
• You organize operator training and handover to operations.

Evolution in the role

BelTech Automation was officially created in January 2025. It is a team under construction and expansion, with the ambition to align our support models for production and projects in Belgium.

This could lead to growth opportunities in technical, project, and management areas. The team currently consists of 15 internal members and more than 80 external collaborators.

Interested? For this role, we’re looking for the following education, experience, and skills

Bachelor or Master degree in automation.
Minimum 5 years’ experience in GMP process automation.
Strong knowledge of PCS7 and/or AVEVA SP
Fluent in French and English.
Strong design, execution, and validation skills.
Excellent communication and leadership abilities.
Risk management and adaptability in dynamic environments.

Be part for 24/7 guard support (level 2) in hybrid model with Automation Integrators, and ready to travel a limited period of time.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

RWE Strategy Lead, Developed Brands (BE) (Anderlecht, Brussels, BE)

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We are looking for a RWE Strategy Lead Developed Brands, Immunology who is collaborative, solutions-oriented, and passionate about leveraging real world data to improve the patient experience to join our HTA and Payer Team. This role can be based in Europe, either at our headquarters in Brussels, Belgium, or at one of our primary hubs in Monheim, Germany or Slough, United Kingdom. The position is also available in multiple locations across the United States. This hybrid role requires a minimum of 40% on-site presence and 5-10% domestic and international travel.

About the Role
You will lead the development and execution of global real-world evidence (RWE) strategies that support the value, safety, effectiveness, and patient impact of UCB’s therapies. You will identify critical evidence needs for existing product lifecycle and translate them into further integrated RWE, epidemiology, outcomes research, and data strategies that inform regulatory, market access, reimbursement, and business decisions, while supporting and expanding our patient access reach. This strategic leadership role requires a deep understanding of evidence generation, healthcare data, and the evolving external landscape. You will drive the use of innovative study designs, registries, real-world data sources, and emerging technologies to address key evidence gaps and ensure decision-makers have the insights needed to improve outcomes for patients. Success in this role requires scientific expertise, strategic thinking, and the ability to influence complex evidence agendas while balancing diverse stakeholder needs and long-term business priorities.

Who you’ll work with

Internally, you will work with colleagues across Real World Evidence, Medical Affairs, Clinical Development, Pharmacovigilance, HEOR, Market Access, Safety, Epidemiology, Patient Impact, and Data & Analytics functions to shape evidence strategies, identify evidence gaps, and generate insights that support and defend , reimbursement, and business decisions.

Externally, you will work with academic researchers, healthcare data providers, registry organizations, contract research organizations (CROs), scientific experts, and industry stakeholders to advance evidence-generation initiatives, access relevant data sources, and ensure the delivery of high-quality, decision-grade evidence.

What you’ll do

Develop and co lead integrated real-world evidence (RWE), epidemiology, outcomes research, and data strategies that support UCB’s assets across the product lifecycle.
Identify evidence gaps and define research plans that address regulatory, market access, reimbursement, safety, and patient-centered evidence needs.
Shape evidence-generation strategies using real-world data, registries, external control arms, innovative study designs, and other fit-for-purpose methodologies.
Anticipate evolving scientific, regulatory, and business challenges and translate them into actionable evidence solutions and investments.
Oversee the execution of RWE studies and programs, ensuring delivery on time, within budget, and in accordance with quality and governance standards.
Drive alignment across complex evidence-generation activities, balancing the needs of multiple stakeholders while maximizing impact and efficiency.
Provide strategic guidance on topics including disease burden, natural history, comparative effectiveness, long-term outcomes, drug utilization, safety commitments, and health technology assessment requirements.
Leverage emerging technologies, including AI-enabled approaches, to enhance data strategy, evidence generation, and decision-making.
Mentor and develop RWE talent while contributing to the continued growth of evidence-generation capabilities across the broader organization.
Represent UCB externally through engagement with scientific experts, research partners, and industry initiatives to advance the use and impact of real-world evidence.

Interested? For this role we’re looking for the following education, experience and skills
Minimum Experience/Skills Required:

Master's degree, PhD, MD, or equivalent advanced degree in Epidemiology, Public Health, Health Economics & Outcomes Research (HEOR), Biostatistics, Life Sciences, or a related discipline.
8+ years of experience within the pharmaceutical, biotechnology, healthcare, or academic sectors with demonstrated involvement in evidence generation, clinical development, market access, regulatory, and/or payer-related initiatives. Experience with Big Data and AI is an advantage
Strong understanding of real-world evidence (RWE), epidemiology, outcomes research, and healthcare data sources.
Experience developing evidence strategies that support regulatory, reimbursement, clinical, and business decision-making.
Demonstrated ability to lead complex initiatives and influence stakeholders in a matrix environment.

Preferred Qualifications

Formal training in epidemiological research methods, outcomes research, health economics, or related quantitative disciplines.
Experience developing and executing integrated RWE strategies for or with pharmaceutical assets across multiple stages of the product lifecycle.
Prior leadership experience, including mentoring, coaching, and developing individuals or leading cross-functional teams.
Expertise supporting health authority, payer, HTA, or market access interactions through evidence generation.
Experience in Immunology, Dermatology, Respiratory, or other specialty therapeutic areas.
Familiarity with innovative study designs, registries, external data sources, AI-enabled technologies, and advanced evidence-generation methodologies.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

QC External Partner Lead BE (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a QC External Partner Lead who is collaborative, strategic, and quality-driven to join our Patient Supply Quality Control team, based at our UCB campus located in Braine-l’Alleud, Belgium or in Bulle, Switzerland.

About the role

As QC External Partner Lead, you will play a key role in strengthening and governing UCB’s global external Quality Control network. You will build strong partnerships with third-party laboratories and service providers, lead governance and improvement initiatives, and drive projects that enhance quality, compliance and efficiency, across the Patient Supply Quality Control organization. You will work in a highly collaborative environment where your expertise, leadership, and problem-solving skills will help shape the future of QC operations.

Who you will work with

You will work closely with Quality Control laboratories, Patient Supply Quality teams, Procurement, Regulatory Affairs, and external partners worldwide. You will lead cross-functional committees, collaborate with internal and external stakeholders, and contribute to a culture of operational excellence, innovation, compliance, and continuous improvement.

What you will do

You will manage UCB’s global network of external QC partners and laboratory service providers.
You will lead governance activities and chair the Analytical Supplies & Services Network Committee.
You will negotiate and oversee contracts, budgets, and performance indicators with external partners.
You will identify risks, coordinate mitigation plans, and ensure regulatory and quality compliance.
You will lead transformation programs and projects that improve QC capabilities, processes, and efficiency.
You will foster a culture of operational excellence, empowerment, safety, and continuous improvement.

Interested? For this role, we are looking for the following education, experience, and skills:

Master’s degree in Science, Pharmacy, Chemistry, Biotechnology, or a related discipline.
Significant experience within pharmaceutical Quality Control and analytical testing environments.
Experience managing external partners such as CMOs, CROs, laboratories, or suppliers.
Strong project management, risk assessment, and cross-functional stakeholder leadership skills.
Excellent communication and negotiation abilities in both French and English.
Proven ability to drive quality improvements, governance, and decision-making in complex environments.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien·ne de laboratoire en microbiologie (Bulle, Gruyere, CH)

Faites la différence pour les patients

Nous recherchons un·e Technicien·ne de laboratoire en microbiologie (Microbiology Laboratory Technician), une personne curieuse, autonome et dotée d’un fort esprit d’équipe, pour rejoindre notre département Quality Operations, basé sur notre site de production biotechnologique, pharmaceutique et chimique de Bulle, en Suisse.

Concernant le rôle

Le poste consiste à effectuer les essais analytiques conformément aux instructions reçues et dans le respect des exigences de qualité (résultats exacts et fiables), des délais, de la conformité technique, ainsi que des règles d’hygiène, de sécurité et de protection de l’environnement.

Le rôle est principalement basé sur des horaires de journée, avec un week-end travaillé par mois.

Vous travaillerez avec…

Vous reporterez au QC Microbiology & EM Team Leader et ferez partie d’une équipe de 10 personnes évoluant dans un environnement collaboratif, dynamique et bienveillant.

Vos activités

Effectuer les tests microbiologiques (bioburden, pureté de culture, endotoxines) pour la production (IPC, DS et autres), conformément aux instructions de travail, aux procédures établies et aux Pharmacopées en vigueur (européenne, américaine et japonaise).
Effectuer les analyses d’eau (WFI, eau purifiée, eau process, etc.) : TOC, pH, conductivité, bioburden et endotoxines.
Réaliser les prélèvements d’air et de surface en zone de production.
Réaliser les prélèvements d’eau en zone de production ou en zone technique.
Participer aux audits internes et externes.
Initier des incidents et des déviations dans le système qualité et contribuer aux investigations associées.
Participer à la rédaction des procédures et méthodes du département.

Intéressé/e ? Pour ce poste, vous devez posséder la formation, l'expérience et les compétences suivantes :

CFC de laborantin·e en microbiologie ou titre jugé équivalent (CFC en biologie ou diplôme technique de niveau Bac+2).
Au moins 2 ans d’expérience dans un laboratoire qualité ; une expérience en environnement GMP constitue un atout.
Maîtrise des techniques d’analyse liées aux activités du poste (H-UPLC, GC, KF, UV, IR, ELISA, potentiométrie, bioburden, endotoxines, TOC, etc.).
Maîtrise des outils Microsoft Office (Excel, Word, Access) ; la connaissance d’un LIMS (Laboratory Information Management System) constitue un atout.
Grand sens de l’organisation et rigueur dans l’application des procédures.
Excellentes compétences en communication et parfaite maîtrise du français, à l’écrit comme à l’oral.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Key Account Manager Sr. / Huntington WV (Huntington, West Virginia, US)

Make your mark for patients

We are looking for a Key Account Manager Sr. (KAM) in Rare Diseases who is patient-focused, exceeds sales objectives, and has worked in a complex selling environment to join us in our Rare Syndromes ∙ Epilepsy US team, based in Huntington, WV.

About the role

Who you’ll work with?

What you’ll do

Exceed sales objectives by implementing marketing initiatives by developing and implementing business plans
Maximize impact by leveraging all available data sets and stakeholder input
Seek qualified leads and effectively profile new accounts, refine call planning/routing to optimize schedules
Working knowledge of the local managed care reimbursement
Emphasizes accountability and the highest standard of ethical conduct.

Interested? For this role, we’re looking for the following education, experience, and skills

Minimum qualifications

Bachelor's degree BA/BS
7+ years of Biotechnology/Biopharmaceutical sales experience
4-6+ years years of rare/orphan drug experience
Proven, documented track record of delivering consistent sales results
Experience calling on customers at a variety of call points (i.e., academic centers, community-based hospitals and private practice offices) both in person and virtual

Preferred Qualifications:

Promoting products specific to CNS/neuroscience, including epilepsy
New product launch experience
Specialty pharmacy/REMS experience

This positions reasonably anticipated base salary range is $150,000 - $210,000 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Non-Clinical Safety Lead - Belgium (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

To strengthen our Non-Clinical Safety Evaluation group within Early Clinical Development and Translational Science, we are looking for a talented individual for the role of Non-Clinical Safety Lead, based in Braine L'alleud, Belgium or Slough, UK or Cambridge, MA (USA).

About the role

As a Non-clinical Safety Lead, you will provide scientific leadership for non-clinical safety across discovery and development programs. You will shape non-clinical strategies, ensure high-quality execution, and support regulatory interactions from early development through clinical progression and post approval. You will:

Lead, communicate, and execute non-clinical safety strategies aligned with clinical development goals.
Develop integrated non-clinical safety plans supporting innovative programs. Ensure timely delivery of high-quality non-clinical data and global regulatory documentation.
Represent UCB in interactions with regulatory authorities and external partners.

This role is well suited to an experienced toxicologist—ideally with exposure to gene and cell therapy or other novel modalities—who enjoys working at the interface of science, development strategy, and regulation. You will thrive in an environment where you can share expertise across functions and global UCB sites, engage with cutting-edge science and build collaborative networks to drive cross-functional success.

What you'll do

Provide non-clinical safety expertise to discovery and development projects
Define, lead, and implement non-clinical safety strategies across programs.
Partner with clinical teams to ensure robust preclinical data supports clinical trial design.
Contribute to global regulatory submissions (e.g., IBs, Briefing Books, INDs, NDA/BLAs) and interact with regulatory authorities.
Oversee the design, review, and interpretation of non-clinical studies.
Manage non-clinical safety programs, including budgets.

Interested? For this role you’ll need the following education, experience and skills

PhD in Toxicology, Pharmacology, or related discipline (or equivalent MS/DVM with experience).
5+ years in non-clinical safety (preferably in pharma or biotech).
Deep understanding of regulatory processes and regulatory toxicology.
Experience managing and forecasting non-clinical safety budgets.
Ability to produce high-quality reports and submission documents with subject matter expert support.

Preferred Qualifications:

Accredited or registered toxicologist.
Experience in gene and cell therapy and/or other novel modalities.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Principal Programmer, Raleigh, NC (Raleigh, North Carolina, US)

Make your mark for patients

We are looking for a Senior Principal Programmer (Statistical Computing Environment Business Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization and Reporting team, based inRaleigh, NC or Atlanta, GA.

About the role

You will help clinical programming teams move to and work confidently within UCB’s modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups, support compliant platform operations, and help improve the way teams generate, validate, and deliver clinical trial analysis and reporting outputs.

Who you’ll work with

You will work with the Programming, Visualization and Reporting team, statistical programming teams, platform administrators, Biometrics partners, and business stakeholders. You will connect technical and business needs, support users through onboarding and daily operations, and help teams follow consistent, compliant, and practical ways of working.

What you’ll do

You will review and coordinate clinical trial analysis and reporting setup requests, making sure they are complete, accurate, and delivered on time.

You will configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements.

You will manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes.

You will coordinate environment provisioning with platform administrators so study teams can begin work in a ready and reliable environment.

You will support programming teams during onboarding, transition from legacy systems, and ongoing operations as a first-line technical contact.

You will improve lifecycle management and workflows by documenting processes, supporting validation activities, and automating practical solutions that enhance quality and user experience.

Interested? For this position you’ll need the following education, experience and skills:

You bring 5+ years of experience in clinical trial results generation, reporting, and submission processes.

You have experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements.

You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings.

You have worked in regulated pharmaceutical environments and understand SDLC, validation, audit readiness, and compliant configuration expectations.

You can communicate clearly with technical teams and business stakeholders, while tracking setup processes across systems and teams.

You bring practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Grants Lead (US) (Smyrna, Georgia, US)

Make your mark for patients

We are looking for a Senior Medical Grants Lead who is curious, collaborative, and purpose-driven to join our Medical Grants and External Funding team, based either out of our offices in Raleigh, NC or Atlanta, GA. This is not a remote role.

About the role:

As the Senior Medical Grants Lead, you will serve as UCB’s global subject matter expert for medical grants and external funding, leading grant review and approval processes while driving operational excellence, governance, and continuous improvement to ensure funding decisions align with medical strategy, scientific merit, patient benefit, and compliance requirements.

Who you will work with:

You will join a global Medical Grants and External Funding team that values trust, curiosity, and shared purpose, working closely with medical, compliance, legal, finance to support clear, balanced, and responsible funding decisions.

What you will do:

Facilitate the review process of medical grant requests, ensuring decisions are based upon scientific / medical merit and safeguarding patient’s welfare

Identify and drive process and system related improvements leading to efficiencies and process excellence

Partner with internal stakeholders and external healthcare organizations.

Provide training that builds funding knowledge and confidence.

Lead, coach, and mentor funding professionals to support high-performance, care, and shared accountability.

Interested? For this role, we are looking for the following education, experience, and skills

Degree in life sciences, pharmacy, healthcare, public health, business, or related field.

Advanced degree in science, public health, business, pharmacy, or equivalent preferred.

8+ years of experience in grants, external funding, medical affairs, or related work.

Experience in global, matrixed organizations with cross-functional collaboration.

Knowledge of healthcare regulations, funding governance, audits, and compliance expectations.

Curious, collaborative approach with strong communication and process improvement skills.

Salary Range:

This position’s reasonably anticipated base salary range is $148,000 to $194,300 per year. The actual salary offered will consider internal equity and may also vary depending on the candidate’s region, job-related knowledge, skills and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

RWE Strategy Lead, Developed Brands (UK) (Slough, Berkshire, GB)

Make your mark for patients

What you’ll do

Develop and co lead integrated real-world evidence (RWE), epidemiology, outcomes research, and data strategies that support UCB’s assets across the product lifecycle.
Identify evidence gaps and define research plans that address regulatory, market access, reimbursement, safety, and patient-centered evidence needs.
Shape evidence-generation strategies using real-world data, registries, external control arms, innovative study designs, and other fit-for-purpose methodologies.
Anticipate evolving scientific, regulatory, and business challenges and translate them into actionable evidence solutions and investments.
Oversee the execution of RWE studies and programs, ensuring delivery on time, within budget, and in accordance with quality and governance standards.
Drive alignment across complex evidence-generation activities, balancing the needs of multiple stakeholders while maximizing impact and efficiency.
Provide strategic guidance on topics including disease burden, natural history, comparative effectiveness, long-term outcomes, drug utilization, safety commitments, and health technology assessment requirements.
Leverage emerging technologies, including AI-enabled approaches, to enhance data strategy, evidence generation, and decision-making.
Mentor and develop RWE talent while contributing to the continued growth of evidence-generation capabilities across the broader organization.
Represent UCB externally through engagement with scientific experts, research partners, and industry initiatives to advance the use and impact of real-world evidence.

Interested? For this role we’re looking for the following education, experience and skills
Minimum Experience/Skills Required:

Master's degree, PhD, MD, or equivalent advanced degree in Epidemiology, Public Health, Health Economics & Outcomes Research (HEOR), Biostatistics, Life Sciences, or a related discipline.
8+ years of experience within the pharmaceutical, biotechnology, healthcare, or academic sectors with demonstrated involvement in evidence generation, clinical development, market access, regulatory, and/or payer-related initiatives. Experience with Big Data and AI is an advantage
Strong understanding of real-world evidence (RWE), epidemiology, outcomes research, and healthcare data sources.
Experience developing evidence strategies that support regulatory, reimbursement, clinical, and business decision-making.
Demonstrated ability to lead complex initiatives and influence stakeholders in a matrix environment.

Preferred Qualifications

Formal training in epidemiological research methods, outcomes research, health economics, or related quantitative disciplines.
Experience developing and executing integrated RWE strategies for or with pharmaceutical assets across multiple stages of the product lifecycle.
Prior leadership experience, including mentoring, coaching, and developing individuals or leading cross-functional teams.
Expertise supporting health authority, payer, HTA, or market access interactions through evidence generation.
Experience in Immunology, Dermatology, Respiratory, or other specialty therapeutic areas.
Familiarity with innovative study designs, registries, external data sources, AI-enabled technologies, and advanced evidence-generation methodologies.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technical Lead, Patient Support Solutions (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Technical Lead, Patient Support Solutions to join our Digital Technology team based out of Atlanta, GA (hybrid, 40% onsite)

About the role

The Technical Lead, Patient Support Solutions partners with the UCB business unit teams to lead projects, use technology systems, and manage technical support resources (internal and/or external) to support patient support/experience programs.

Who you’ll work with

This role will work closely with internal stakeholders (Patient Support Program, Data & Reporting, Marketing etc.) as well as external vendors & partners.

What you’ll do

Possesses the ability to analyze, manage, implement, train end-users, and support technical systems and associated business processes.
Assists with technology specifications and implementation plans.
Provides technical and business analyst expertise involving the design, development, construction and on-going support of systems, processes, integrations, or methods.
Provide technical support in the deployment of purchased application as well as overseeing system design, development, implementation, and maintenance of internally developed applications. Involved in defining, managing, and supporting interfaces between multiple vendors and systems.
Provides strategic business analyst expertise of systems, processes, or methods.
Responsible for delivering attainment of project plans, milestones, deliverables, and financial targets for assigned projects and programs.
Engage with key stakeholders to develop trusted relationships
Serve as the IT SME for U.S. Patient Support Programs. Maintain awareness of industry trends, identify opportunities for business process and technology improvements and value creation.
Support the evaluation, selection, and management of vendors and partners.

Interested? For this role we’re looking for the following education, experience and skills

Required:

Bachelors Degree
7+ years’ experience in full systems life cycle management and deployment experience
4+ years of experience in the pharmaceutical or healthcare industry related to Patient Support/Experience Programs (Data aggregators, co-pay and reimbursement partners, specialty pharmacies and third-party data sources, etc.)

Preferred:

Experience in the support of computerized System Validation, part 11 compliance
Experience with technology systems to support commercial/go-to-market teams in the life sciences industry
Strong understanding of HIPAA requirements (Data Security, Encryption, storage, handling, etc) and associated system impacts.
Thorough understanding of project management methodology and system development lifecycle principles, validation & qualification

This positions reasonably anticipated base salary range is $124,000-163,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

埼玉：QA Manager (Saitama, Saitama, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

【チームについて】

埼玉工場の関連部門と日常的に協働し、品質を起点に現場の課題解決をリードします。また、国内だけでなく海外の品質チームとも連携しながら、より良い結果に向けて議論し、合意形成を進める組織環境です。

【主な業務内容】

本ポジションは、埼玉工場での品質の仕組みを最新状態に保ち、日本市場への安定供給を支える役割です。現場に根差した視点で品質と生産性の両面を高め、メンバーの成長も後押しします。

・製造所および市場向けの出荷判定を行う
・日本市場へ高品質な製品を安定供給する
・品質の仕組みを整備し、法規制と社内基準へ適合させる
・主要指標の目標達成に向けて改善を推進する
・メンバーを支援し、教育とスキル向上を促進する
・安全・衛生・環境の活動に参画し、影響を低減する

【応募資格】

・医薬品又は医薬品部外品のQA経験３年以上
・英語力（英語での会議参加、資料作成、メール対応ができること）

（あれば尚可）
・薬剤師資格
・出荷判定業務経験

（求める人物像）
・医薬品に関する専門知識、経験をお持ちの方
・文書の作成・照査を体系的に行い、適切に運用できる方
・部門横断の課題に対する原因究明と再発防止を推進できる方
・国内外の関係者と戦略的に連携できるコミュニケーション力のある方

【応募方法】
・日本語の履歴書、職務経歴書と英語のCVを1つのファイルにまとめ、システムにアップロードしてください
・UCB社員からの紹介がある場合は、応募時にその旨をシステム上でご記載ください

（English follow）

Job Summary

Assure Quality of products manufactured at Saitama site and released to Japan market by developing and maintaining the up-to-date Quality System per the local regulations and UCB requirements.

Major Accountabilities/Responsibilities

1. Quality Assurance
- Supply good-quality products seamlessly to Japan market.
- Develop and maintain the up-to-date Quality System at Saitama site and assure that Quality System is fully aligned with the latest requirements by local HA, guidelines related to pharmaceutical industry and UCB Quality Policies/Standards.
- Achieve the relevant KPI targets.
- Made decision of batch release from the site and for the market.
2. Support and Training
- Support associates to achieve site/team/manager/personal goals.
- Develop associate’s knowledge and skills.
3. Continuous improvement
- Engage in OE activities and enhance quality and/or productivity at Saitama site.
4. HSE
- Engage in HSE activities and assure own and associate’s health/safety.
- Minimize the impact on environment.
5. Corroboration with Global QA organization and other organizations.
- Raise awareness of other organizations and work together to achieve better results.

Experience : More than 5 years’ experience working under GMP (QA, QC, Production or equivalent), General knowledge about pharmaceutical drugs and production

Competencies

【GMP／専門知識】
• GMPに基づく文書を体系的に、また適切な内容で作成する能力を有する。また、照査する能力を有する。
• 他部門も関わるプロジェクトのリーダーとして適切にGMP業務の遂行を管理監督できる能力を有する。大規模な工程・施設・設備・装置に関わるプロジェクトをプロジェクトリーダーとして遂行できる能力を有する。
• 全般的にGMPを広く理解しており、製造所全体の業務に反映することができる能力を有する。
• GMP以外のGxP分野との関係性全般を理解している。
• PIC/S、ICH等国際的な規制を理解し業務に反映できる能力を有する。
• 製造所全体の品質システムの改善を提案、遂行できる能力を有する。
• 関係する法規制、ガイドラインについて、自部門内および他部門に対して指示/教育することができる能力を有する。
• グローバルの活動に貢献できる工程、施設、設備、装置の知識を有する。
• 安全および５Sに関する深い知識を有し、実際の作業・工程・施設・設備・装置に反映することができる能力を有する。
• 工程、施設、設備、装置を深く理解し作業の全体を管理、遂行できる能力を有する。
• 工程のトラブルに適切に対応する能力を有する。
• 日本や埼玉工場のGMPオペレーションや法規制について説明することができ、プロセス変更等の協議に参加し、着地点を見つけることができる。

【ビジネスリテラシー、コミュニケーション能力、リーダーシップ】
• 法規・法令と会社および職場のルール・マナーを自ら遵守するともにチームメンバーにもルール順守を徹底させることができる。
• 期待される業務を遂行できるように自らの生活・健康を管理することができる。また、チームメンバーの健康に配慮することができる。健全な職場環境づくりを主導できる。
• 業務遂行のため工場内、関連部署およびグローバルのコミュニケーションを戦略的に行える能力を有するとともに、外部ステークホルダーと有益な関係を構築するコミュニケーション能力を有する。
• グローバルおよび埼玉工場のObjectivesを理解し、自部門および自分個人のObjectivesと関連付けられる能力を有する。
• 埼玉工場の概要を理解し、Visitorに説明できる。特に自部門の業務内容に関しては深く理解し、説明できる知識を有する。英語でも説明できる。
• グローバルの会議に参加し、協議できる英会話能力を有する。英語で説明資料を作成することができる。英語でメールでのコミュニケーションができる。また、英語のGMP文書などを理解することができる能力を有する。
• 基本的な経理・財務の仕組みや用語を理解でき、予算管理、発注業務や、投資効果や損益の評価を実行できる能力を有する。

• 報告、連絡、相談を適切に行えるだけでなく、戦略的にコミュニケーション能力を発揮し、利害関係者や、チームメンバーと良好な関係を確立し、スムースに業務を進める能力を有する。
• 相互尊重を具現化できる。他者の意見を積極的に求めて真摯に受け止め、議論を尽くして結論を導き出すことができる。また、チームに相互尊重の場を展開できる。
• 自部門内および部門を横断する高度な、またグローバルも関わる問題・課題に対して、問題解決・原因究明・再発防止の策定および実行を主導できる。
• 担当業務の責任範囲において多面的な情報と自らの経験および知識を活用して適切なリスクを取りながら最適な判断をすることができる。
• 皆で決定することに貢献し、決定したことは責任をもって実行するとともに、部門を横断して（工場内、関連部署内）他者にも明示して実行させることができる。
• 個々人の能力を引き出し、チームの能力を最大限引き出す能力を有する。
• PVSプリンシプルを理解し、実行する能力を有する。
• チームメンバーにPVSプリンシプルを説明し、実行を求めることができる。
• 成長に対する情熱をもち、計画的に学習できる能力を有する。
• チームメンバーを鼓舞し、チームのモチベーションを醸成する能力を有する。
• 関係者からの相談から、前向きな思考となるように助言できる。

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBで働く魅力

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

Directeur des Ventes - Region Ouest (Field Based, Field Based, FR)

Faites la différence pour les patients

Nous recherchons un(e) Directeur(trice) des Opérations Terrain / Ecosystem Lead qui soit un leader collaboratif, stratégique et orienté résultats pour rejoindre notre équipe Direction Immunologie – Franchises Dermatologie. Régions Ouest et Sud-Ouest de la France.

À propos du poste

Le/la Directeur(trice) des Opérations Terrain / Ecosystem Lead pilote une équipe dédiée à la promotion des produits et solutions UCB afin d’atteindre les objectifs stratégiques de la franchise. Il/elle développe les compétences de son équipe, garantit l’excellence opérationnelle et coordonne l’écosystème des parties prenantes afin de maximiser la valeur pour les patients, les professionnels de santé et l’entreprise. Il/elle collecte également les insights terrain et contribue à l’évolution de la stratégie UCB.

Avec qui travaillerez-vous ?

Vous intégrerez la Direction Immunologie, en collaboration étroite avec les équipes terrain, les fonctions siège, les équipes européennes et les différentes parties prenantes de l’écosystème de santé. Vous travaillerez avec les équipes Marketing, Médical, Accès au Marché et les fonctions transverses afin de développer des stratégies intégrées et centrées sur les besoins des patients.

Vos responsabilités

• Manager et développer une équipe terrain performante et engagée.
• Définir, suivre et atteindre les objectifs individuels et collectifs.
• Consolider les business plans et garantir leur exécution efficace.
• Collecter et analyser les insights terrain pour guider la stratégie.
• Développer et piloter l’écosystème des parties prenantes clés.
• Garantir l’excellence opérationnelle et la conformité réglementaire.

Intéressé(e) ? Pour ce poste, nous recherchons les compétences, expériences et qualifications suivantes

• Diplôme Bac+5, pharmacien ou médecin apprécié.
• Minimum 5 ans d’expérience commerciale, marketing, médicale ou accès marché.
• Expérience dans le management d’équipes commerciales ou terrain.
• Leadership, vision stratégique et capacité d’analyse avancée.
• Excellente communication et maîtrise de l’anglais courant.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Gene Therapy Molecular Biology Development Scientist (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Gene Therapy Molecular Biology Scientist who is curious, detail‑oriented, and collaborative to join us in our Analytical Development Sciences team, based in Braine‑l’Alleud, Belgium.

About the role
You will contribute to the development of gene therapy products by designing and delivering molecular biology analytical methods that support product development from early stages through clinical readiness. Working in a regulated laboratory environment, you will help ensure data quality, regulatory compliance, and robust scientific outcomes that ultimately support patients living with severe diseases.

Who you’ll work with
You will be working in a multidisciplinary team of analytical scientists, molecular biologists, and technical experts. You will collaborate closely with colleagues across process development, characterization, vector biology, and external partners, contributing to a shared goal of scientific excellence and patient‑focused innovation.

What you’ll do

Develop and execute molecular biology analytical methods supporting release and stability testing of gene therapy products
Contribute to analytical method development and validation in a regulated laboratory environment
Lead or contribute to the deployment of Next generation Sequencing strategy in the analytical department
Transfer analytical methods to internal teams and external development partners
Review, analyse, and interpret experimental data to support product development decisions
Prepare high‑quality technical documentation in line with regulatory and data integrity standards

Interested?

For this role we’re looking for the following education, experience and skills

Doctorate in molecular biology, or equivalent experience, with at least 2 years of experience in molecular biology analytical method development in a regulated (GxP) environment
Sound understanding of analytical method validation principles
Experience using dPCR and qPCR techniques, ELISA, Western blot, Gel Electrophoresis techniques; proven hands-on experience with NGS is also required
Ability to work independently while contributing effectively within cross‑functional teams

#GeneTherapy

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Non-Clinical Safety Lead - Cambridge, MA (Cambridge, Massachusetts, US)

Make your mark for patients

About the role

Lead, communicate, and execute non-clinical safety strategies aligned with clinical development goals.
Develop integrated non-clinical safety plans supporting innovative programs. Ensure timely delivery of high-quality non-clinical data and global regulatory documentation.
Represent UCB in interactions with regulatory authorities and external partners.

What you'll do

Provide non-clinical safety expertise to discovery and development projects
Define, lead, and implement non-clinical safety strategies across programs.
Partner with clinical teams to ensure robust preclinical data supports clinical trial design.
Contribute to global regulatory submissions (e.g., IBs, Briefing Books, INDs, NDA/BLAs) and interact with regulatory authorities.
Oversee the design, review, and interpretation of non-clinical studies.
Manage non-clinical safety programs, including budgets.

Interested? For this role you’ll need the following education, experience and skills

PhD in Toxicology, Pharmacology, or related discipline (or equivalent MS/DVM with experience).
5+ years in non-clinical safety (preferably in pharma or biotech).
Deep understanding of regulatory processes and regulatory toxicology.
Experience managing and forecasting non-clinical safety budgets.
Ability to produce high-quality reports and submission documents with subject matter expert support.

Preferred Qualifications:

Accredited or registered toxicologist.
Experience in gene and cell therapy and/or other novel modalities.

Salary:

This position’s reasonably anticipated base salary range is $168,000 to $220,500 per year. The actual salary offered will consider internal equity and may also vary depending on the candidate’s region, job-related knowledge, skills and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Process Owner (GPO) - Plan-to-Distribute | Manufacturing, Release & Distribution (Anderlecht, Brussels, BE)

Make your mark for patients

We are looking for a Global Process Owner (GPO) – Plan-to-Distribute | Manufacturing, Release & Distribution to join us in our HQ office in Brussels, Belgium.

About the role

You will play a key role in shaping how the organization structures and governs how products are planned, manufactured, released, and made available for distribution across our global organization.

As Global Process Owner for Plan-to-Distribute, you will own the end-to-end process from production planning through manufacturing, quality release, and inventory readiness, and act as a key guardian of process compliance in the context of ongoing changes and transformations.

You will ensure consistent, efficient, and compliant ways of working across regions and sites. This role is ideal for someone with strong experience in manufacturing or supply operations, combined with a passion for process improvement, standardization, and transformation in a regulated environment.

This is a senior enterprise role requiring the maturity to work through influence in a large, federated stakeholder landscape, bringing coherence across handovers rather than replacing local manufacturing, supply, or quality accountability. Success in this role is reflected in the consistent execution of planning, manufacturing, and distribution processes across regions, improved transparency and control, strengthened compliance, and the ability to enable effective cross-functional collaboration while supporting transformation and business priorities.

Who you'll work with

You will be working in a team that connects expertise across the full value chain and enables a more integrated way of operating across the organization.

The team brings together global process leaders and works closely with manufacturing sites, quality teams, supply chain, engineering, and regional experts.

You will collaborate with stakeholders across functions and geographies, including senior leaders, to align processes and support key transformation initiatives. You will also help build a strong network of process experts and contribute to a culture of continuous improvement and operational excellence.

You will work in partnership with functional leadership teams to connect existing expertise, improve decision quality, and strengthen end-to-end performance across planning, manufacturing, release, and distribution.

What you'll do

Define and govern the global manufacturing and supply process from production planning through manufacturing, quality release, and inventory availability, ensuring consistency across sites and regions

Identify and drive improvements in efficiency, reliability, and compliance by simplifying processes, standardizing practices, and introducing automation where appropriate

Partner with manufacturing, quality, supply chain, procurement and regional teams to align process design and resolve cross-functional challenges

Establish clear standards for documentation, controls, training, and performance management to support compliance, audit readiness, and sustainable operations

Support transformation initiatives by ensuring processes are well designed, integrated across functions, and aligned with both operational and regulatory requirements

Build and develop a community of process experts, promoting best practices and strengthening capabilities in process management across the organization

Shape and support transformation initiatives and major programs (including wave-based deployments) by identifying and prioritizing process improvement opportunities, guiding end-to-end process design, and ensuring alignment across functions, systems, and governance, in partnership with business and functional teams responsible for implementation and adoption

Support structured change adoption by contributing to change impact assessments, defining adoption priorities, and ensuring business readiness and stakeholder alignment, while partnering with functions accountable for execution, training delivery, and post-implementation stabilization

Interested? For this role we’re looking for the following education, experience and skills

Strong experience in manufacturing, supply chain, or production operations within complex international organizations

Around 15 years of professional experience, ideally in life sciences, pharmaceuticals, or another highly regulated industry

Solid understanding of production planning, manufacturing execution, quality release, and inventory management processes

Experience with process improvement methodologies such as Lean or Six Sigma; certification is an advantage

Strong stakeholder management skills, with the ability to influence, challenge constructively, and build alignment across functions and senior levels

Ability to work across processes and systems with a focus on end-to-end outcomes rather than individual tools

High emotional intelligence, resilience, and the ability to navigate a large stakeholder ecosystem with credibility and diplomacy

Excellent English communication skills are required; additional languages may be beneficial depending on stakeholder scope

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Bio DS Operations Quality Manager Weekend (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

To strengthen our Bio DS Quality we are looking for a talented profile to fill the position of: Bio DS Operations Quality Manager Weekend – Braine l’Alleud, Belgium

About the role

You will ensure the quality oversight of activities specifically related to upstream (USP), downstream (DSP) and Media & Buffer (M&B) manufacturing operations within UCB’s new commercial biologicals drug substance facility at our Braine campus.

This role is crucial in ensuring compliance with regulatory and internal standards, ensuring a continuous presence of the operational quality team on the floor, ensuring quality systems (Deviation, CAPA, CC) are followed and ensuring batches are released. The Bio DS Operations Quality Manager ensure that all these activities are performed in a solution-oriented mindset.

As this is a new facility, the role requires actively leading and coaching the team through the launch phase, adapting to the challenges and realities of the initial years of operation. Additionally, this role involves connecting to peers (business and quality) within B7 and UCB organization to ensure knowledge sharing and to build a solid network.

You will work with

In this role, you will collaborate closely with manufacturing teams operating the biologics production process (USP, DSP, and Media & Buffer), while leading and coaching a team of GMP Facilitators. You will work in partnership with colleagues from Quality Assurance, Quality Control, MSAT, Regulatory Affairs, and other site quality leaders to ensure manufacturing activities remain compliant, batches are released on time, and quality issues are resolved efficiently. As the weekend quality lead, you will also play a key role in connecting weekend and weekday teams to ensure seamless communication and consistent quality standards across the site.

What you will do

Leadership and Management

Build, lead and manage the Weekend Quality Operations team, including hiring, training, and performance management.
Develop people capability & knowledge. e.g: by implementing training matrix and coaching for GMP Facilitators.
Ensure day-to-day quality oversight of the manufacturing operations by GMP Facilitators.
Ensure a constant alignment with QA peers to provide a consistent quality support.
Ensure a consistent approach to team management, performance follow-up, and employee development across the USP, DSP, and M&B organizations, in alignment with weekday teams and site expectations.
Perform continuous feedback within Quality Operations team and with Manufacturing counterparts.
Participate on the Bio DS Quality Operations Lead Team and act as deputy for Bio DS Quality Operations Head when needed.
Participate on regular alignment meeting with local and Global business partners (i.e., Manufacturing, MSAT, Quality Assurance Support, Quality Control, Regulatory)
Be part of/Challenge all MSAT process improvement.
Propose solutions on major and critical issues encountered in USP, DSP and M&B manufacturing.
Influence on way of working of other local department.

Quality Assurance

Responsible for the effective management of quality systems, including deviations (events), CAPA, batch review, change control, documentation, etc. Guarantee appropriately assessed from a quality perspective and are closed in time.
Responsible for the effective and right-first-time batch review process and intermediate batch release process.
Ensure all Process Orders (POs) related to manufacturing activities are released.
Organize thorough review / approval of GMP documentation and their appropriate application (e.g., gembas, spot checks, shopfloor).
Ensure quality representatives are involved in case of significant events occurring during manufacturing activities.
Review and approve major or critical deviations, CAPA and Change Control.
Actively participate to the quality governance in place within the organization.
Ensure consistency in the management and resolution of quality events across weekend and weekday teams.
Act as a key liaison between weekend and weekday organizations to guarantee effective communication, escalation, and transfer of quality-related information.
Support the implementation of quality improvements by ensuring alignment of practices, lessons learned, and decisions across all shifts and teams.

Regulatory Compliance

Performs internal inspections.
Assist and / or explain topics related to USP, DSP and M&B activities if requested during an internal or external inspection.
Ensure critical / major risks related to inspection readiness are appropriately escalated. Ensure relevant mitigations and documentation are available (e.g., power point presentation, preventive actions).
Participate in reviewing Annual Product Reviews.

Interested? For this position you’ll need the following education, experience and skills

Bachelor’s, master’s degree or an education in a relevant scientific discipline

Minimum of 5 years’ experience in the pharmaceutical industry within Quality Assurance
Demonstrated experience in Upstream ou Downstream Biologicals drug substance
Demonstrated leadership experience, with the ability to make autonomous decisions and drive results independently
Good command of English, both written and spoken
On-site presence required
Ability to face unstable environment and demonstrate agility to handle unpredicted changes
Able to remain effective and maintain sound judgment under pressure

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Science Liaison Sr. / Dallas (Dallas, Texas, US)

Make your mark for patients

UCB is looking for an experienced, science-driven and patient-focused Sr. Medical Science Liaison (MSL) to work with the Myasthenia Gravis Team to strengthen our neurological Rare Disease Organization’s (RDO) mission for the team in the Texas Region, which currently includes Texas, Arkansas & Oklahoma .

About the Role

The MSL provides peer-level scientific exchange with clinicians and researchers working in neuromuscular diseases. This role fosters collaborative, science-driven partnerships with key stakeholders to support optimized patient care. The MSL will provide scientific exchange, contribute insights to medical strategies, and drive patient-focused initiatives within the local health ecosystem.

Who you will work with

Internal partners: Medical Affairs (including Medical Directors), Real-World Evidence (RWE), Clinical Development/Operations, Medical Information, Compliance/Legal, and cross-functional commercial colleagues (e.g., sales, marketing, market access).
External partners: healthcare providers and key opinion leaders (KOLs), clinical investigators, medical decision-makers in health systems/IDNs, and patient advocacy organizations.

What you’ll do

Maintain deep therapeutic-area expertise by staying current on pre-clinical and clinical data, treatment options, emerging standards of care, and competitive landscape for myasthenia gravis and other neuromuscular disorders.
Develop and manage trusted, peer-to-peer relationships with key stakeholders (e.g., KOLs, clinical investigators, medical groups/IDNs, patient advocacy groups) and execute tailored engagement plans to identify local needs and opportunities.
Deliver balanced scientific exchange and clinical value propositions, including addressing medical information inquiries and providing effective, audience-tailored presentations to internal and external audiences.
Generate and communicate meaningful medical insights from the field to inform medical strategy and tactics, including input for creation and updates of Standard Response Letters.
Represent UCB as a scientific expert at local, regional, and national conferences where issues related to the diagnosis and treatment of neuromuscular diseases are addressed.
Identify and support research and educational collaboration opportunities, including feasibility assessment and primary liaison support for unsolicited Investigator-Initiated Studies (IIS) from inception through publication.
Collaborate cross-functionally (e.g., Medical, RWE, access, and other partners) to enhance patient care, support access engagements with medical expertise as needed, and contribute to broader Medical Affairs projects.

Interested? For this position, you'll need the following education, experience and skills:

Minimum Qualifications:

Doctoral level degree (PharmD, PhD, MD, DO, or DNP); Nurse Practitioners with research and/or clinical expertise in a related field and advanced training/education may be considered.

Minimum 1+ years of medical affairs experience in the biopharmaceutical industry.

Must reside within the assigned territory.

Valid driver’s license and ability to travel up to 60% in the designated territory.

Preferred Qualifications:

Relevant therapeutic area experience in neurology, neuromuscular, and/or rare diseases

Strong business acumen with a solid understanding of the pharmaceutical industry.

Ability to clearly articulate complex scientific concepts in 1:1 and group settings.

Basic knowledge and understanding of health, economic principles and clinical trials.

Experience in partnership with Global and local therapy area experts and external organizations

Must be a strong team player and effectively interface with other internal departments including regional business units, marketing, sales, medical affairs, and clinical operations.

Creative approach to problem solving and able to work effectively in a constantly changing environment.

Strong interpersonal skills and excellent verbal and written communication skills.

Strong time management and organizational skills with proficiency in Microsoft applications.

Ability to work independently and manage a large territory with multiple stakeholders

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Strategy & Med. Info. Lead Neuro (Seoul, Seoul, KR)

Make your mark for patients

We are looking for a Medical Strategy & Med. Info. Lead Neurology to join us,based in Seoul,Korea.

About the role

Identifies and fosters purposeful partnerships with key scientific influencers to drive new sources of patient value. Converses in two-way scientific interactions, disease state and treatment algorithm discussions optimizing understanding of UCB therapies for the right patient segments in a scientific and balanced manner within the local health ecosystem. Collaborates to advance local patient value oriented initiatives i.e., Medical, RWE) with key stakeholders

Guides the assessment, planning and implementation activities to ensure maximum patient and stakeholder value creation, and fulfillment of nPVU strategies.

Ensures that individuals have the training, market knowledge and resources to effectively support individual liaisons and partners in driving patient value creation and achieving nPVU business objectives.

Ensure UCB Operational Compliance to the highest professional standards. The expectation is that compliance is a part of how we operate. Compliance violations may lead to disciplinary action including impact on annual appraisals. Adherence to compliant behavior is an expectation at UCB.

What you’ll do

Key Activities:

• Play key role by via medical activities for launch readiness of upcoming pipelines

• Support the development of UCB population health strategies for gaining adoption of UCB approaches for improving diagnosis, treatment and overall management of epilepsy and movement disorders in ways that create patient value, advance stakeholder objectives and increase use of nPVU medicines where appropriate.

• Shares best practices in engagement and proposal process to secure data, findings and publications that document new perspectives on patient value creation with UCB promoted products across ecosystems and patient segments in accordance with Neurology RWE data strategy plan.

• Agile and proactive identification and management of key scientific and medical influencers based on local ecosystem dynamics and stakeholder needs and drivers (from push to pull)

• Exploration and identification of new sources of patient value (innovative solutions and services)

• Manage and generate product/ disease state data (IIS, audits, RWE etc.)

• Support clinical studies, clinical development and share insights with R&D team

• Serving as the leading local scientific expert for UCB solutions

• Oversight UCB cares partner’s activities on medical information handling

Key Deliverables:

• Partners with key clinical stakeholders to advance medical initiatives, in defined strategic areas, to drive optimal patient care. Also, partner with other stakeholders like payers, patient organizations and patients might be relevant depending on the available resources within local organization.

• Provides scientific expertise and interpretation to strategic initiatives in collaboration with other local Partner roles

• Shares insights, innovation opportunities and patient needs internally to the PVU and New Meds

• Capitalizes on RWE and uses them to further reinforce the value that UCB solutions bring to patients.

• Proactively engages relevant stakeholders to move the UCB medical & scientific agenda forward

• Acts as Single Point of Contact (SPOC) for a (select) pre-determined list of HCPs and connects customers to the right UCB resource as needed

• As needed, plays a role in optimizing the understanding of UCB therapies for the right patient segments through a deep scientific and product knowledge

• The Affiliate Medical Information Personnel

− Perform Medical Information activities in line with Core Global Medical Information (MI) Standards sop-008513.

− Perform Medical Information activities in compliance of global and local requirements and regulations.

Interested? For this role we’re looking for the following education, experience and skills

• At least 7+ years in stakeholder facing roles within healthcare industry

• Fluent in Korean (writing and speaking)

• Demonstrated experience leading multidisciplinary and/or matrixed teams

• Bachelors’ degree in life sciences or healthcare required

• PharmD, PhD or MD preferred

• Knowledge of appropriate regulatory guidelines

• Demonstrated leadership skills in managing, developing, and influencing teams

• Demonstrated excellence in written and verbal communications

• Demonstrated strength in business planning, tactical plan development and execution

• High Compliance Awareness (CIQ)

• Strategic planning and Problem solving

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Head of Advanced Analytics (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Global Head of Advanced Analytics who is Collaborative, Curious, and Impact‑oriented to join our Integrated Insights team, based at our UCB offices in Raleigh, North Carolina or Atlanta, Georgia, United States.

About the role

You are going to nurture a global advanced analytics vision that strengthens how UCB creates value for patients. You will enable data‑led decision making, foster the use of advanced analytics and responsible artificial intelligence, and help transform complex questions into meaningful, human‑centred insights. You will shape how UCB balances scientific depth with patient‑focused understanding, ensuring that insights support better choices across the full lifecycle of our assets.

Who you will work with

You will collaborate with a supportive, multidisciplinary community across Integrated Insights, Patient Evidence, Patient Solutions, and Patient Impact. You will work closely with insight partners, global and regional stakeholders, and colleagues across scientific, commercial, and technical domains. You will be part of an environment that values curiosity, shared learning, and co‑creation to deliver integrated insights that matter for patients.

What you will do

• You will enable a forward‑looking vision for advanced analytics across UCB

• You will be responsible for shaping data‑led insight generation enterprise‑wide

• You will manage a global team fostering technical depth and business fluency

• You will co‑create priorities with global, regional, and local stakeholder groups

• You will ensure impactful analytics projects answer the questions that matter most

• You will nurture collaboration between technical experts and business partners

Interested?

For this role, we are looking for the following education, experience, and skills:

• 13-15+ years of experience enabling advanced analytics, data science, and artificial intelligence

• Bachelor's degree required, Master's degree preferred

• Ability to translate complex needs into actionable insight opportunities

• Experience working in matrix environments with multiple stakeholder groups

• Strong problem‑solving mindset with curiosity and structured thinking

• Ability to interpret model outputs and identify potential model limitations

• Experience fostering talent development and collaborative team cultures

The reasonably anticipated salary range for this position is $236,800-310,800 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Qualification and Validation Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

UCB is embarking on one of the most significant investments in its history through the development of a new state-of-the-art biologics manufacturing campus in Georgia, USA.

We are looking for talented, curious and ambitious individuals who want to make a lasting impact and contribute to shaping the future of biologics manufacturing at UCB.

We are looking for a Qualification and Validation Lead who is collaborative, rigorous and proactive to join us in our Internal Manufacturing team, based in our UCB campus in Braine-l’Alleud, Belgium.

About the role

This role is contributing to the design and delivery of a future-ready biologics manufacturing facility. You will ensure that manufacturing systems, equipment and processes are designed and delivered in compliance with regulatory and quality requirements. You will contribute to building a compliant and inspection-ready facility by integrating validation principles throughout the project lifecycle in a rapidly evolving project environment.

Who you’ll work with

You will be working in a team that collaborates with manufacturing sites, quality experts and project stakeholders. The team focuses on ensuring compliance, alignment with regulatory expectations and readiness for inspections working across different time zones.

What you’ll do

Develop, implement, and lead the overall Qualification and Validation strategy for the entire site, while ensuring its successful execution and ongoing compliance across all operations.
Define and represent qualification and validation requirements across the project.
Ensure compliance with regulatory and quality standards throughout design and delivery.
Review and assess technical documentation related to validation activities.
Contribute to inspection readiness and support audit and regulatory interactions.
Translate operational and regulatory expectations into project requirements.
Promote strong quality and compliance culture across stakeholders.

Interested? For this role we’re looking for the following education, experience and skills

More than 10 years of relevant experience in qualification and validation within regulated environments.
Experience in greenfield or brownfield projects.
Experience in biotech is mandatory.
Knowledge of GMP requirements and regulatory expectations.
Experience supporting audits and regulatory inspections.
Strong ability to analyse and interpret technical documentation.
Strong communication and collaboration skills.
Willingness to adapt to project variabilities and a rapidly evolving work environment.
Fluent in English; French is an advantage.
Occasional travel to the United States may be required during conceptual design and basic design phases.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of IT eConnectivity (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Head of Global IT eConnectivity who is visionary, collaborative, and results-driven to join us in our Global Information Technology Infrastructure & Services team, based in ou office in Braine-l’Alleud, Belgium.

About the role

We are looking for an experienced leader to shape the future of our global network and connectivity landscape. In this role, you will be responsible for defining and delivering the strategy, services, and operations that enable secure, reliable, and efficient connectivity across our global organization.

You will lead a well-established team while driving the next phase of transformation and innovation. This role blends strategic vision with operational excellence, requiring a leader who can confidently engage with senior stakeholders, manage complex budgets, inspire high-performing teams, and remain closely connected to the technology decisions that drive measurable business outcomes and lasting value.

Who you’ll work with

You will be working in a team that delivers critical infrastructure and connectivity services across all company locations worldwide. Reporting to the Head of Global Infrastructure & Services, you will lead a team of managers and specialists while collaborating closely with cybersecurity, digital technology, business stakeholders, and external service partners.

You will work with colleagues across multiple regions and functions, influencing decisions at both operational and leadership levels to ensure secure, compliant, and future-ready connectivity services.

What you’ll do

Define and execute the global connectivity, network, and infrastructure strategy aligned with business priorities, technology roadmaps, compliance requirements, and budget objectives
Lead and develop a global team, fostering accountability, collaboration, talent growth, and high performance across internal and external resources
Oversee the design, delivery, operation, and continuous improvement of secure network services across offices, manufacturing sites, and data center environments
Manage relationships with technology partners and service providers, ensuring service quality, performance targets, contractual commitments, and operational excellence are achieved
Drive innovation and modernization initiatives, identifying new technologies and opportunities that improve security, reliability, scalability, and business value
Lead investment planning and financial governance, managing operational and capital budgets while ensuring efficient use of resources
Partner with senior stakeholders across the organization to strengthen network security, support business transformation, and maintain compliance in regulated environments

Interested? For this role we’re looking for the following education, experience and skills

Bachelor’s or Master’s degree in Information Technology, Computer Science, Engineering, or a related field
At least 8 years of experience in infrastructure or network leadership roles, including a minimum of 5 years managing teams and budgets
Strong knowledge of enterprise networking, network security technologies, and large-scale infrastructure operations
Experience leading global teams and managing both internal employees and external service providers across different geographic regions
Demonstrated experience managing significant operational and capital budgets, ideally within complex multinational environments
Strong stakeholder management, communication, and influencing skills, with the ability to engage effectively at all organizational levels
Professional certifications in project management, technology infrastructure, networking, or related disciplines are an advantage

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Digital Lead, Clinical Analytics (Raleigh, North Carolina, US)

Make your mark for patients

We are looking for a Digital Technology Lead, Clinical Analytics to join our Digital Technology – Clinical Patient Evidence team based out of Raleigh, NC (hybrid)

About the role

This pivotal role centers on leveraging advanced analytics and business intelligence to drive data-informed decision-making across Clinical Operations (GCSO) and digital technology initiatives. The position is responsible for designing and implementing robust analytics strategies that support the full spectrum of clinical trial activities, from planning to execution and optimization.

The ideal candidate will bring deep expertise in data architecture, data engineering, and analytics platforms, combined with strong knowledge of clinical trial systems (e.g., EDC, CDB, external data). The role will champion modern data ecosystems and the adoption of AI, GenAI, and advanced analytics, ensuring that foundational data capabilities are in place to scale these innovations safely and effectively.

Who you’ll work with

This individual will work in close partnership with stakeholders throughout the clinical development and clinical study operations journey, the role identifies opportunities to harness data, uncovers actionable insights, and translates complex analytics into innovative, scalable business solutions.

What you’ll do

Develop and execute the roadmap for clinical analytics, ensuring alignment with organizational goals, initiatives and industry best practices.
Oversee the planning, implementation, and lifecycle management of clinical analytics projects and platforms.
Ensure successful integration of digital solutions with internal and external systems, including CROs, labs, and regulatory partners.
Build and govern AI-ready data pipelines, ensuring: Structured & unstructured data are usable for ML/ GenAI use cases as well as Metadata and context are preserved for model interpretability.
Partner with AI/ Analytics teams to enable: Risk-based monitoring, protocol optimization, trial performance predicition. Ensure ethical, compliant, and bias-aware data usage for AI initiatives
Assume the role of a system owner (ITSO) for designated projects, ensuring end-to-end responsibility for the success of IT implementations, including computerized system validation activities.
Partner with clinical operations, Clinical Data Management, and various Digital Tech teams to define requirements and deliver scalable, user-centric solutions.
Act as the primary liaison between business stakeholders and technology partners (internal/external).
Demonstrate a broad understanding of internal and external data flows, processes in UCB and Drug Development, and act as a business champion for data as a corporate asset and the digitalization process.
Ensure all digital solutions comply with GxP, GDPR, and other relevant regulatory standards.
Oversee validation, documentation, and audit readiness of clinical analytics platforms.
Drive continuous improvement initiatives, leveraging emerging technologies such as AI, automation, and advanced analytics.
Foster a culture of innovation, encouraging the adoption of new tools and methodologies to enhance clinical trial efficiency.
Manage relationships with technology vendors, ensuring service quality, cost-effectiveness, and alignment with business needs.

Interested? For this role we’re looking for the following education, experience and skills

Required:

Bachelors degree in computer sciences or related field
5+ years of experience in an Information Technology environment required with 3 years of experience in the pharmaceutical industry
Ability to use analytical environments like PowerBI, Spotfire, Qlik to discover insights

Preferred:

Experience with key technology services providers and best practices of the industry.
Experience in business and IT process outsourcing and external partner collaboration.
Experience in system integration
Experience in process assessment, analysis, modelling, improvement and automation methodology.
Experience in system validation in the pharmaceutical industry.
Passion for Data Science and developing analytical solutions
Knowledge in advanced analytics (including machine learning) and data mining technologies

This positions reasonably anticipated base salary range is $125,000 - $165,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Marketing Lead Osteo Alps (Bulle, Gruyere, CH)

Make your mark for patients

We are looking for a strategic, collaborative, and results-oriented Marketing Lead Osteo Alps (Switzerland & Austria) to join our team.

About the role

The Marketing Lead Osteo Alps owns the development and delivery of the osteoporosis marketing strategy across Switzerland and Austria. The role is accountable for translating global and regional strategies into impactful local plans, driving omnichannel engagement excellence, and ensuring strong business and patient outcomes through cross-functional leadership.

Who you’ll work with

You will work closely with cross-functional stakeholders including Sales & Marketing Leads, Scientific Leads, Medical & Business Insights, Communications, Market Access, Regulatory, Legal, Compliance, and Supply teams. You will also collaborate with the iEU Strategy Operations Team, local Patient Value Unit partners, healthcare professionals, key opinion leaders, and payer stakeholders. As part of the European Marketing Leads community, you will contribute to regional initiatives and share best practices across markets.

What you’ll do

• Own and shape the Osteoporosis marketing strategy for the Alps region, aligned with global and regional priorities

• Define key growth drivers, customer segmentation, and value propositions based on local insights

• Drive performance through clear KPIs and ensure marketing impact on business and patient outcomes

• Lead the development and continuous refinement of annual Integrated Strategic Plans (ISP) with cross-functional teams

• Translate and drive execution of regional and global osteoporosis strategies into impactful local plans

• Define and drive the development and execution of impactful promotional materials and solutions

• Own and safeguard consistency in strategy, branding, budget and communication excellence

• Own the understanding and optimization of the customer and patient journey, addressing therapy initiation hurdles and tracking impact through KPIs

• Accountable for marketing performance, engagement metrics, and contribution to business objectives within the Osteoporosis portfolio

Interested? For this role we’re looking for the following education, experience and skills

• Bachelor’s degree in Business, Marketing, Life Sciences, or related field

• Experience in the pharmaceutical sector

• 4–6 years’ experience in healthcare marketing and stakeholder engagement, with strong expertise in brand strategy, digital, and omnichannel marketing

• Strong strategic thinking, project management, and cross-functional collaboration capabilities

• High attention to detail, ensuring all brand communications and materials are accurate and consistent, combined with a proactive mindset to identify opportunities and solve problems

• Fluent in German with good working knowledge of French and excellent written and verbal communication skills in Englis

• This is a remote position, with regular opportunities to connect with colleagues during periodic office days at our Bulle site.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Rheumatology Medical Rep＿大阪エリア (Field Based, Field Based, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

JOB SUMMARY
Primary Purpose / Regulatory Responsibilities: UCB製品を必要とする患者さんすべてに届ける担当テリトリーの中で、医師と患者をつなげて最適なアクセスを確立する

MAJOR RESPONSIBILITIES
顧客エンゲージメント戦略策定
①担当エリアの戦略・プランに基づいて、担当テリトリーの短期(今期)の顧客エンゲージメント戦略を立案する。
②担当テリトリーの顧客エンゲージメント戦略策定のために、担当Dr.や患者・競合の動向を情報を収集・整理し、インサイトを導出する。
顧客エンゲージメント向上活動
①担当テリトリーのDr.・HCP・ステークホルダーとの信頼関係を強固にすべく、自身で顧客エンゲージメント活動を推進し、確実に遂行する。
②担当テリトリーにおいて自身が顧客エンゲージメント活動を効果的に推進できるよう、必要な関係者との連携を含め自律的に活動環境を整備する。
戦略・活動の課題分析と改善
①担当テリトリーの顧客エンゲージメント戦略の進捗をモニタリングするために最適なKPIを、担当エリアの戦略・プランと整合するよう設定する。
②担当テリトリーのKPIをタイムリーに確認・分析し、ESLや必要な関係者と連携の上で迅速・柔軟に改善策を策定し実行する。
コンプライアンス遵守
①自身の活動について、関連法規・ガイドライン等に対するコンプライアンス遵守を徹底すると共に、チーム・他者の遵守徹底にも貢献する。
人的リソースプラン策定
①担当テリトリーの顧客エンゲージメント戦略の遂行に必要な関係者(担当者)とゴール・方針を共有し連携する。
②必要な関係者と短期の戦略遂行・活動のために、担当者レベルで信頼関係を構築する。
能力開発(OJT含む)
①スキル強化に関する営業部やチームの取り組みに積極的に参加し、自らの知識・スキル・成功事例を営業部・チームに還元する等を通じて貢献する。
②自身の育成課題を把握し、自律的にスキル強化に取り組み成長する。
パフォーマンスマネジメント
①自身の期待役割を理解した上で適切なパフォーマンス目標を設定、自己評価を行う。
②自身のパフォーマンス評価を理解し、さらなる挑戦やパフォーマンス改善に自律的に取り組む。
組織カルチャー醸成
①高い倫理観を持ち、活力が高く働きがいのある社員エンゲージメントの高いチーム創りやカルチャー醸成に、自らが望ましい行動を体現することで貢献する。

EDUCATION & QUALIFICATION
Education Level: Bachelor's Degree
Other Certification: Medical Representative

COMPETENCIES
課題思考
・上司サポートを受けながら、テリトリーの情報・データから自らで問題を推測でき、業務課題を導出できる。
・上司サポートを受けながら、自らで、課題の原因を整理でき、解決策を設計できる。
・上司のサポートを受けながら、自らで所属組織のビジョン・目標を理解し、企画を設計できる。
課題遂行
・上司サポートを受けながら、自身の目標達成や課題解決のための実行シナリオやアクションプランを自らで作成できる。
・上司サポートを受けながら、自らで実行プロセス・手法を組み立てた上で実行できる。
・上司サポートを受けながら、自身の活動について、自らで状況・環境を鑑みてチェックポイント(指標等)を設定し、進捗を確認できる。
コミュニケーション
・相手のバックグラウンドや置かれた状況、感情を理解し、自身と異なる考え方や意見も受け入れると共に、他者のために意見・助言できる。
・物事の体系・構造を整理し、飛躍や矛盾無く相手に説明し、相手の疑問に的確に回答すると共に他者のために意見・助言できる。
・関係者(顧客・関係部署・その他関係者等)に貢献できること、及び相手に希望することを明確にし、業務で連携すると共に他者のために意見・助言できる。
組織貢献
・他者の考え方や強み、課題、業務への適応状況等を理解すると共に、他者のために意見・助言できる。
・自身への期待を理解し、成長目標を設定した上で自律的に能力開発に取り組むと共に、他者のために意見・助言できる。
・組織の目標を理解し、他者の成果・成功を賞賛し、自身の活動に取り入れると共に、他者のために意見・助言できる。
ベースマインド
・いかなる時でも他責にせず、自分の行動に対して責任を持つと共に、計画的かつ積極的に業務を遂行すると共に、他者のために意見・助言できる。

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBで働く魅力

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

Team Leader M&I Bio (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

À propos du rôle

Avec qui vous allez collaborer

Ce que vous allez faire

Vous allez gérer et encadrer les équipes techniques et sous‑traitants en thermie et métrologie
Vous serez responsable de la planification et de l’exécution des contrôles périodiques des équipements (USP, DSP, laboratoires, bioréacteurs, centrifugeuses, BSC,…).
Vous allez superviser les contrôles préventives et curatives des équipements.
Vous veillerez au respect des exigences GxP, qualité, sécurité et environnement.
Vous piloterez la performance au travers de KPI et assurerez l’alignement avec les objectifs du service.
Vous allez rédiger et/ou revoir et/ approuver les documents de contrôle périodique conformément aux Bonnes Pratiques de Fabrication
Vous allez garantir la conformité GMP, HSE et la qualité documentaire.
Vous allez développer les compétences de l’équipe et assurer leur formation continue.
Vous assurerez la gestion des déviations, audits et actions correctives dans les délais.
Vous allez suivre les Actions Correctives et Préventives (CAPAs) et les Changes Controls (CC).
Vous allez participer activement aux audits et inspections réglementaires.
Vous favoriserez un environnement de travail collaboratif et performant.

Intéressé·e ? Pour ce rôle, nous recherchons les compétences et qualifications suivantes

Diplôme de Bachelier en électromécanique ou expérience équivalente.
Expérience en thermie, métrologie ou contrôle technique en environnement réglementé.
Bonne connaissance des exigences GxP, HSE et des systèmes qualité.
Expérience en management d’équipe technique.
Capacité à analyser des processus et à identifier des axes d’amélioration.
Excellentes compétences en communication, assertivité et gestion des parties prenantes.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Insight Generation Manager (Tokyo, Tokyo, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

English Follows

■ポジション概要
Insight Generation Managerは、事業部門の成長戦略をデータとインサイトの力で支援するポジションです。市場データ、営業データ、調査データ、デジタルデータなどを活用し、ビジネス上の重要課題に対する分析や示唆を提供します。
事業部門やグローバルチームと連携しながら、予測分析、アドバンスドアナリティクス、市場調査、パフォーマンスマネジメントを通じてデータドリブンな意思決定を推進し、事業成長に貢献いただきます。

■採用部門について
Insight Generationチームは、営業・マーケティング・メディカル・ファイナンス・デジタル・ITなど幅広い部門と連携しながら、データ分析およびビジネスインサイトの創出を担う組織です。
戦略立案や意思決定につながるインサイトへと変換し、事業部門の成長を支援する重要な役割を担っています。

■主な業務内容

事業部門の課題やニーズを把握し、データ分析を通じて意思決定を支援する
市場データ・営業データを活用した分析プロジェクトを企画・推進する
Advanced Analyticsを活用し、事業課題の解決や成長機会の特定をリードする
分析結果をビジネス視点で解釈し、実行可能なインサイトとして提言する
短期・中長期の売上予測モデルを構築し、事業計画策定を支援する
市場環境や主要ドライバーの変化を分析し、業績への影響を可視化する
KPIの設計・モニタリングを行い、経営層やグローバルチームへのレポーティングを担う
オムニチャネル施策やプロモーション活動の効果測定を行い、デジタル戦略の最適化を支援する
市場調査の設計・分析を通じて、顧客や市場のインサイトを創出する
IQVIA、JMDC、MDV等のデータソースを活用し、ビジネス課題に応じた最適な分析基盤を構築する

■ポジションの魅力

データ分析から事業戦略まで幅広く関与できる
経営層や事業責任者との距離が近く、高い影響力を発揮できる
AI・機械学習など最新アナリティクスを活用する機会がある
グローバルチームとの連携を通じて国際的なキャリア形成が可能
製薬業界におけるビジネスインテリジェンス・コマーシャルエクセレンス領域の専門性を高められる

■応募要件

製薬会社またはコンサルティングファームでの実務経験
製薬業界におけるBusiness Intelligence、Insight Generation、Commercial Excellence、事業企画、マーケティング分析等の経験
製薬企業が保有する各種データを活用したインサイト創出・戦略提言の経験
コンサルティングファーム出身の場合、製薬企業向けプロジェクトの担当経験
IQVIA、JMDC、MDVなど製薬業界のセカンダリーデータを活用した分析経験
データ分析結果を経営・事業戦略へ結び付けた経験

■歓迎要件

希少疾患領域の担当経験

ーーーーーーーーーーーーーーーーーーーーーーーーーーーーーーー

JOB SUMMARY

Primary Purpose / Regulatory Responsibilities:
The primary purpose of a Insight Generation Manager (IG Manager) is to navigate responsible business unit to achieve anticipated business growth suggesting recommended resource allocation through providing business insights ensuring data driven decisions and driving performance management discussion and provides meaningful reports / insights to business partners

IG Manager needs to
- oversee and ensure the quality of value creation by the team in the space of insight generation, performance management, analytics (inc. advanced analytics)
- provides strategic insights and guidance to BUs(Business Units) for their critical business and organizational decision making
- be a partner seamlessly and transversally with key internal stakeholders to ensure alignment with business teams and digital teams
- build business cases to evaluate pipeline assets/future events
- discover/validate new data sources to generate insights refining strategies and tactics

MAJOR RESPONSIBILITIES

Project lead
Lead and facilitate all analytical projects in Japan
Gather and detect stakeholders’ needs, and interpret them into business questions
To solve business questions, IG Manager makes a decision the proper approach, and assign the suitable members, then leads the analytics projects (e.g. advanced analytics, market research, SFE, secondary data deliver, etc.)
Proactively share the analytics knowledge with global members

Forecasting
Build clear, accurate, and well-structured forecast models that align marketing strategy
Decide assumptions for building sales forecast (short-term to long-term forecast)
Quantify the sales impact by each critical business factor
Prepare the documents to explain the forecast logic for business review

Analytics (inc. Advanced Analytics)
Develop solid analytics logic and conduct the analysis to solve business questions
Connect and interpret analytical results with business situation and explain the results with business story
Have the basic knowledge about AI, deep learning, machine learning and can communicate with AI engineer smoothly
Understand what AI can do and cannot do

Digital
Define / monitor KPI for Omni-channel projects to track their progress
Manage promotion data (physical + digital) analysis projects to evaluate promotion effectiveness
Deliver insights to improve / enhance digital initiatives through data analysis

Performance Management
Identify metrics that drive performance against strategic priorities
Analyze and reports performance metrics to management
Share KPI reports with global stakeholders at fixed intervals

Data Knowledge
Deeply understand the definitions of data source (e.g. IQVIA, JMDC, MDV, etc.)
Identify the ideal data source for each business question

Market Research
Propose the best method and creates questionnaire to answer business questions
Analyze primary data to deep-dive the points needed to quantify

EDUCATION & QUALIFICATION

Bachelor's Degree

Post Graduate Qualification in Relevant Discipline Preferred e.g. MSc, PhD, MBA

Project Management Certification or Qualification Preferred (e.g. PMP, APM, Prince 2, Agile etc)

Experience : More than 5 year experience in pharmaceutical industry is preferable (Not only focus on the length. Broadly understanding the industry is important.)

Excel / PowerPoint skills (Advanced)

Language : Japanese / English : Business

Having working experience in Commercial excellence department in pharma is preferable

COMPETENCIES

Collaborative / respectful mindset
Able to promote collaboration with various departments (marketing, sales, medical, business development, pricing, finance, data management, IT, digital, global stakeholders, etc.) as a hub person.

Communication (understands other people’s needs and intensions)
Ability to understand stakeholder needs correctly and quickly
Ablet to explain the results of the analysis in a way that is understandable to people in BU

Challenging spirit
Demonstrates a challenge to new things in behavior
Actively participate in new initiatives and pave the way for building the UCB future

Enterprise thinking
Have a perspective that provides values to the whole company or to the whole BUs, not focusing on a specific department or function

Resilience towards flexible thinking and working environment
Able to deliver values in a rapidly changing environment by having flexible thinking and a can-do mindset

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBで働く魅力

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

QC Devices & Packaging Technician (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous cherchons un·e Analyste Contrôle Qualité qui est rigoureux·se, orienté·e solution et collaboratif·ve pour nous rejoindre dans notre équipe Incoming Packaging, basée dans notre campus UCB situé à Braine-l'Alleud, Belgique.

À propos du rôle

Vous allez jouer un rôle clé dans le contrôle qualité des articles de conditionnement (primaires, secondaires et dispositifs médicaux) et dans la réalisation de tests de fonctionnalité. Vous contribuerez activement à la libération des lots dans SAP et au bon fonctionnement du laboratoire.

Avec qui vous allez travailler

Vous rejoindrez une équipe dynamique au sein du département Contrôle Qualité, où la collaboration, la précision et la sécurité sont au cœur de nos activités. Vous travaillerez en étroite collaboration avec d'autres analystes, superviseurs et services transverses.

Ce que vous allez faire

• Effectuer des contrôles qualité sur les articles de conditionnement et produits finis.
• Être responsable de réaliser des tests de fonctionnalité sur les dispositifs médicaux.
• Gérer l’enregistrement des données brutes et le double check analytique.

• Assurer la réception et le suivi des échantillons et du matériel de laboratoire.
• Contribuer à la conformité HSE et à la politique sécurité du laboratoire.
• Suppléer vos collègues analystes en cas de besoin.

Intéressé·e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes

• Minimum un Bachelier en chimie, biochimie ou microbiologie.
• Expérience en laboratoire de contrôle qualité ou environnement similaire.
• Connaissance des articles de conditionnement et dispositifs médicaux.

• La maîtrise de SAP est atout.
• Sens du détail, rigueur et respect des procédures.
• Esprit d’équipe et engagement envers la sécurité.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

US Bio Manuf. Drug Substance Expert (Atlanta, Georgia, US)

Make your mark for patients

About the role

Who you'll work with

What you'll do

Serve as biomanufacturing process expert for facility design decisions.
Align manufacturing capabilities with future biologics pipeline requirements.
Provide technical guidance on process equipment and facility layouts.
Lead cross-functional reviews and technical decision-making activities.
Author and review technical documentation and operational standards.
Support startup readiness and successful facility implementation.

Interested? For this role we're looking for the following

Minimum requirements

Doctorate with 6+, master's with 10+, or bachelor's with 15+ years' experience.
Experience in biologics development, manufacturing, engineering, or process sciences.
Expertise in mammalian antibody drug substance manufacturing processes.
Experience leading technical decisions within complex cross-functional organizations.
Strong technical writing and document review experience.
Willingness to travel and eventually relocate to Georgia.

Preferred requirements

Expertise in upstream processing, including cell culture and bioreactors.
Expertise in downstream purification and filtration technologies.
Experience supporting large-scale biologics facility design projects.
Knowledge of quality, compliance, and regulatory requirements.
Experience influencing senior stakeholders across global organizations.
Experience supporting greenfield manufacturing facility startups.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Team Leader Mesure et Instrumentation ZAC (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Team Leader Mesure & Instrumentation (ZAC – Zones à Atmosphère Contrôlée) orienté·e équipe, structuré·e et techniquement solide pour rejoindre notre équipe basée sur notre campus UCB à Braine‑l’Alleud, Wallonie, Belgique.

À propos du rôle

Vous allez encadrer, organiser et coordonner les équipes techniques en charge des activités de contrôle périodique des équipements et des locaux en ZAC. Vous garantirez la bonne exécution des activités dans le respect des exigences GxP, qualité et sécurité. Vous jouerez un rôle clé à la fois opérationnel et technique en pilotant la performance et en contribuant à l’amélioration continue des activités du service.

Avec qui vous allez collaborer

Vous travaillerez en étroite collaboration avec les équipes BelTech, engineering, maintenance, IT, production et HSE. Vous serez en interaction continue avec les sous‑traitants et les utilisateurs internes. Vous jouerez un rôle central dans la coordination des activités entre les différents services du site.

Ce que vous allez faire

Vous allez gérer et encadrer les équipes techniques internes et externes en environnement ZAC.
Vous allez superviser les contrôles préventives et curatives des équipements.
Vous serez responsable de garantir de la planification et de la réalisation des contrôles périodiques ZAC des équipements et des zones.
Vous piloterez la performance au travers de KPI et assurerez l’alignement avec les objectifs du service.
Vous allez rédiger et/ou revoir et/ approuver les documents de contrôle périodique conformément aux Bonnes Pratiques de Fabrication
Vous allez garantir la conformité GMP, HSE et la qualité documentaire.
Vous veillerez au respect des exigences GxP, qualité, sécurité et environnement.
Vous assurerez la gestion des déviations, audits et actions correctives dans les délais.
Vous allez suivre les Actions Correctives et Préventives (CAPAs) et les Changes Controls (CC).
Vous allez participer activement aux audits et inspections réglementaires.
Vous allez favoriser un environnement de travail collaboratif et performant.
Vous allez développer les compétences de l’équipe et assurer leur formation continue.

Intéressé·e ? Pour ce rôle, nous recherchons les compétences et qualifications suivantes

Diplôme de Bachelier en électromécanique ou expérience équivalente.
Expérience en zones à atmosphère contrôlée (ZAC) ou environnement technique similaire.
Bonne connaissance des exigences GxP, HSE et systèmes qualité.
Expérience en management d’équipe et coordination multi‑parties prenantes.
Capacité d’analyse et d’optimisation des processus.
Excellentes compétences en communication et assertivité.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

VIE Bioanalytical Scientist (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Le site de Braine-l’Alleud est spécialisé dans la synthèse chimique, le développement, la fabrication et le conditionnement de produits pharmaceutiques.

Pour plus d’information : www.ucb.com

Votre mission:

Nous recherchons un(e) scientifique junior pour rejoindre l’équipe de bioanalyse du département Precision Medicine à Braine-l’Alleud. Vous contribuerez au développement de méthodes bioanalytiques de pharmacocinétique (PK), principalement via des techniques LBA (MSD), avec une exposition possible au LC-MS, afin de soutenir la transition des candidats médicaments vers le développement clinique.

Responsabilités principales:

Participer au développement, à l’optimisation et au troubleshooting de méthodes bioanalytiques (principalement LBA).
Acquérir une compréhension de la bioanalyse PK et de son rôle dans les projets NBE.
Contribuer aux activités de laboratoire, de la phase de développement à l’analyse et l’interprétation des données.
Travailler en collaboration avec des équipes multidisciplinaires.
Appliquer les bonnes pratiques de laboratoire, les exigences qualité et l’intégrité des données.
Développer progressivement votre autonomie dans un environnement dynamique et encadré.

Votre profil :

Diplôme de bachelier minimum, avec expérience en LBA et/ou spectrométrie de masse (autres techniques de laboratoire acceptées).
Poste basé à Braine-l’Alleud pour une durée de 12 mois, prolongeable.
Contribution au développement d’essais pharmacocinétiques (PK), principalement via des technologies LBA (MSD), avec exposition possible au LC-MS.
Participation aux activités de développement bioanalytique : mise au point, optimisation et analyse de données.
Intégration au laboratoire de bioanalyse avec une progression vers une autonomie croissante dans les activités expérimentales et l’interprétation des résultats.

Veuillez noter que ce programme est en partenariat avec Business France, et que nous suivons les conditions requises par Business France pour effectuer une mission VIE. Les principales conditions de participation sont les suivantes:

•    Avoir entre 18 et 28 ans;
•    Détenir la nationalité d’un pays membre de l’Espace Economique Européen ;
•    Ne pas avoir travaillé ou vécu dans le pays où aura lieu la mission ;
•    Etre disponible pour se consacrer à la mission à temps plein ;
•    Si vous êtes de nationalité ou de double nationalité française, être en règle vis à vis des obligations de service national de la France (Numéro Identifiant Défense) ;
•    Avoir un casier judiciaire vierge.

Si vous ne remplissez pas l'ensemble de ces conditions, nous ne pourrons pas tenir compte de votre candidature.

Global Medical Head - Integrated & Strategic Evidence Generation (Anderlecht, Brussels, BE)

Make your mark for patients

We are looking for a Global Medical Head - Integrated Evidence Generation who is strategic, collaborative and curious to join us in our Medical Communities team, based in our Headquarters office in Brussels, Belgium.

About the role

You will drive the development and execution of the integrated evidence generation plan for designated medicines and indications. Working globally, you will help identify evidence needs, set priorities, guide study planning and ensure evidence activities meet the needs of healthcare stakeholders and create patient value. You will partner with internal and external stakeholders to deliver meaningful, timely and robust evidence.

Who you'll work with

You will be working in a team that connects global strategy and evidence planning cross-functionally and across geographies. You will partner closely with global medical, access, clinical and RWE leaders, evidence generation community colleagues, internal subject matter experts and external collaborators. You will also be supported by an operational manager to help deliver evidence plans effectively.

What you'll do

Provides a strategic overview of activities for the asset to the Asset (Medical Community) Team in terms of gaps, priorities, tactics, delivery and expected impact
Develops asset evidence generation strategy and ensure timely development & maintenance of the plan in line with Asset strategy to ensure maximal impact
Works closely with Product Global Medical Head and other internal / external stakeholders to understand evidence needs, derive evidence generation priorities and identify opportunities for evidence generation partnerships
Facilitates cross-functional plan and alignment
Communicates key decisions to relevant stakeholders
Develops budget for the asset to execute on the plan
Ensures regular revision and update of evidence generation strategies relative to new available knowledge
Ensure studies within the plan are aligned to strategy and represent best investment for impact
Leads ISEG project proposal approval for each studies coming into the plan
Ensures timely delivery of the Plan supporting the asset strategy
Oversees execution to successfully deliver highly relevant and robust evidence in a timely manner
Enhances and track performance and progress through management and monitoring of key metrics and incentives (KPIs)
Leads the prioritization and strategic planning of Post Hoc analyses and is accountable for their delivery in due time

Interested? For this role we're looking for the following education, experience and skills

Minimum 5-7 years of pharmaceutical or biotechnology experience, including product launch and Medical Affairs/Market Access/Clinical Development experience
Demonstrated experience at regional/global level in delivering integrated evidence generation strategy, planning and execution to successfully deliver robust evidence maximizing the asset’s long-term value to patients
Strong experience and skills in data interpretation and impactful communication to internal and external stakeholders. Broad understanding of methodologies for robust data generation, with experience in RWE and observational study planning/execution.
Experience in establishing successful external stakeholder interactions and collaborations as part of medical strategy execution.
Strong Strategic and business acumen. Anticipation of industry trends; Ability to critically analyze complex data
Mastery of therapeutic area & assets knowledge and ability to translate science into clinical patient value and business value.
Demonstrated experience and knowledge in clinical/RWE study development and management and sound understanding of statistical process and analysis
Leads with executive presence, strong emotional intelligence, integrity, business acumen, humility, respect, transparency and positively influence performance excellence
Strong communication skills, ability to articulate complex subjects with clarity, ease and executive presence (story telling skills)
Excellent interpersonal and relationship building skills; establishes trust and partnership collaboration with cross-functional leadership, internal colleagues and external collaborators
Digital & AI Fluency: Has the ability to identify and leverage digital technologies, data, and AI-enabled solutions to enhance evidence generation, decision-making, and organizational impact
Adaptability: comfortable working with complexity in a fluid environment

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Utilities Technician (Bulle, Gruyere, CH)

Make your mark for patients

Nous recherchons un·e Technicien·ne Utilités – Domaine d’expertise: HVAC.

Autonome, rigoureux·se et orienté·e solutions pour rejoindre notre équipe Technical Support & Utilities, basée dans nos bureaux de UCB à Bulle, Suisse.

À propos du poste

Vous serez responsable de l’exploitation et de la maintenance des systèmes utilitaires industriels et propres, en garantissant leur performance, fiabilité et conformité aux normes cGMP et HSE. Vous contribuerez à l’amélioration continue, participerez aux audits et soutiendrez les projets d’investissement et de qualification.

Avec qui vous travaillerez

Vous collaborerez étroitement avec les équipes internes telles que l’ingénierie, la qualification, le support & méthodes, la métrologie et l’automation. Vous coordonnerez également les prestataires externes et ferez partie de l’organisation de piquet.

Vos missions

Exploiter et maintenir les installations utilitaires industrielles et propres
Réaliser et superviser les maintenances préventives et correctives
Diagnostiquer les pannes et assurer le redémarrage rapide des installations
Participer aux projets d’investissement et à la qualification des systèmes
Préparer et contribuer aux audits internes et externes
Appliquer et promouvoir les politiques HSE et cGMP du site

Intéressé·e ? Voici les compétences, formations et expériences requises

CFC ou formation technique équivalente
Expérience en exploitation et maintenance d’utilités industrielles
Connaissance des environnements contrôlés (zones propres, ATEX)
Maîtrise du français et anglais technique
Compétences en électricité, automation, hydraulique et pneumatique
Maîtrise des outils SAP PM et Pack Office

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

IT & Digital Procurement Category Manager (UK) (Slough, Berkshire, GB)

Make your mark for patients

We are looking for a Global Procurement Manager for IT & Digital who is strategic, influential, and deeply knowledgeable about technology to join our Procurement team at UCB, based out of Slough, UK.

About the Role

As the Global Procurement Manager IT & Digital, you will ensure the organization secures optimal value when acquiring technology including software, hardware, and telecom solutions. You will collaborate closely with Digital Technology business leaders to understand organizational needs, assess technology vendors, negotiate optimal commercial terms, and proactively manage a global technology spend. Your strong, current knowledge of IT and digital trends will enable you to make informed decisions and drive procurement excellence across multiple regions and regulatory landscapes.

Who You’ll Work With

You will work closely with Digital Technology leadership, cross-functional internal stakeholders and strategic suppliers. Operating within a global remit, you will build productive supplier relationships, partner with internal teams to support business needs, and act as a key advisor on technology sourcing, risk management, and sustainability requirements.

What You’ll Do

Manage a global Technology spend and oversee end-to-end technology procurement processes.
Develop and implement technology category strategies to drive proactive spend management.
Identify opportunities to optimize technology spend and enhance supplier value.
Build and maintain strong relationships with internal stakeholders and strategic suppliers.
Identify potential suppliers and lead supplier selection efforts.
Manage complex RFI/RFP processes using procurement-approved tools.
Provide fact-based sourcing recommendations considering market dynamics and competitive trends.
Negotiate commercial terms and ensure contractual compliance in partnership with Legal.
Embed risk management and sustainability requirements into supplier contracts.
Support continuous improvement initiatives and approve POs within defined thresholds.

Interested? For this role we’re looking for:

Minimum 8 years’ experience in strategic procurement, sales, or digital technology roles.
Strong negotiation and supplier management experience, especially within technology domains.
Excellent communication, stakeholder engagement, and leadership skills.
Deep understanding of the IT/Digital landscape, with curiosity and adaptability in a dynamic environment.
Team-oriented, collaborative mindset with commitment to diversity and inclusion.
Fluent in English.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Procurement Category Lead - Market Insights & Patient Services (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Global Procurement Category Lead - Market Insights & Patient Services who is strategic, value‑driven and highly collaborative to join our Global Procurement department, based in Brussels, Belgium or Atlanta, Georgia.

About the Role
As Global Procurement Category Lead - Market Insights & Patient Services, you will lead global procurement strategy across Research, Data Acquisition, Medical & Patient Services. You will unify procurement approaches across regions, build strategic supplier partnerships, and ensure sourcing strategies support both business objectives and scientific priorities.

In this highly visible leadership role, you will help shape the future of data, research, and patient services procurement by driving value creation, strengthening supplier performance, enhancing compliance, and supporting innovation across the enterprise. You will lead global category teams and work closely with senior stakeholders to ensure procurement is recognized as a strategic business partner.

Who You’ll Work With
You will report to the Global Head of Marketing, Selling & Impact Procurement and collaborate closely with senior leaders across Insights, Medical Affairs, Patient Services, Market Access, Legal, Compliance, Information Security, and Finance. You will also lead and develop procurement teams across multiple regions while managing relationships with strategic suppliers and external partners.

What You’ll Do

Develop and execute global category strategies across research procurement, data acquisition, and medical and patient services procurement.
Lead and develop global category teams, ensuring alignment to common standards, governance, and strategic priorities.
Build and manage strategic relationships with research agencies, data providers, and patient services vendors.
Negotiate and oversee complex commercial agreements, including data licensing, research services, and patient support contracts.
Drive value creation through supplier optimization, commercial innovation, and improved return on research and data investments.
Partner with business stakeholders to align sourcing strategies with scientific, medical, and commercial priorities.
Ensure compliance with data privacy, healthcare regulations, and third‑party risk management requirements.
Shape procurement approaches related to digital, data, and AI‑enabled solutions while supporting responsible innovation.
Embed sustainability, supplier diversity, and ESG principles into procurement strategies and supplier selection processes.

Interested? For this role we’re looking for:

Bachelor’s degree required; Master’s degree preferred in business, life sciences, or a related field.
Significant procurement leadership experience across market research, data licensing, medical services, or patient services categories.
Strong experience leading global teams and influencing senior stakeholders within complex matrix organizations.
Knowledge of data privacy regulations, healthcare compliance frameworks, and third‑party risk management.
Strong commercial, negotiation, and supplier relationship management capabilities.
Digital and data fluency, with experience in analytics, AI governance, or data‑driven decision‑making.

This positions reasonably anticipated base salary range is $172,500-230,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Patient-Centered Outcomes Research (PCOR) Lead (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Patient-Centered Outcomes Research (PCOR) Lead who is strategic, collaborative, and insightful to join our Patient-Centered Outcomes Research (PCOR) team, based at our UCB headquarter located in Brussels, Belgium, or in our offices in Monheim Germany, or Slough UK.

About the role

As a PCOR Lead, you will play a leading role in the development and implementation of patient-reported outcomes (PRO) and more broadly clinical outcome assessment (COA) strategies. You will generate robust patient experience data and evidence that demonstrate the meaningful patient benefits of our innovative UCB solutions and that meet external evidentiary standards and support healthcare decision-making.

Who you will work with

As a member of the Patient-Centered Outcomes Research team, you will collaborate with cross-functional teams, eg, representatives from Clinical Development, Medical Affairs, Health Economics and Outcomes Research, Market Access, Regulatory Affairs, and Biostatistics.

What you will do

You will lead the development and implementation of patient experience evidence strategy on clinical outcome assessments (COAs) from early development through to full lifecycle management.
You will lead research activities supporting the selection, development, validation, interpretation, and implementation of PRO/COA measures.
You will provide subject matter expert input into strategic documents, tactical plans and target patient value profiles, as well as into clinical documents, eg, study protocols, analysis plans, clinical reports.
You will provide subject matter expert input into regulatory and HTA briefing packages and interactions..
You will lead scientific dissemination (eg, peer-reviewed publications, abstracts) in line with publication strategies.
You will build relationships and partner with external groups to advance methodological frameworks and acceptance of patient experience evidence to inform external healthcare decision making.
You will be an inspiring ambassador to contribute to organizational awareness on the value of patient experience evidence.

Interested? For this role, we are looking for the following education, experience, and skills:

Master's degree, PhD, MD, or equivalent qualification in a relevant scientific discipline.
Significant experience in biopharmaceutical, medical device, or academic environments within PRO/COA, or patient preference research.
Expertise in PRO/COA development, validation, and implementation in clinical research, including strong knowledge of qualitative and quantitative scientific methodologies and evidentiary requirements by regulatory and HTA bodies
Experience in clinical development, regulatory and HTA interactions.
Excellent stakeholder management, communication, influencing, and cross-functional collaboration skills in a matrix organization.
Proven project leadership capabilities with experience managing complex global initiatives

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Commercial Operations Analyst (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Commercial Operations Analyst who is intellectually curious, adaptable and analytical to join us in our Contracts & Pricing Team, based in our Atlanta office in Georgia, United States. This hybrid role (at least 40% of the time in office) is limited to 10% travel domestically.

About the Role
You will be responsible for supporting payer and Pharmacy Benefit Manager (PBM) contracting operations with significant financial and operational impact. This role ensures the timely and accurate administration of Commercial, Managed Care, Trade, and Medicare Part D contracts and rebate programs through detailed data analysis, contract maintenance, pricing validation, and reimbursement management.

Who you’ll work with
Acting as a Subject Matter Expert (SME) and Single Point of Contact (SPOC) for assigned payer and PBM accounts, the Commercial Operations Analyst partners with Market Access, Finance, Sales, Compliance, Legal, IT, and external stakeholders to resolve complex contract and reimbursement issues, optimize revenue performance, and drive operational excellence. Through the analysis of large and complex utilization, pricing, and rebate datasets, this role supports contract execution, forecasting, compliance requirements, system enhancements, and strategic initiatives that strengthen patient access and business outcomes.

What you’ll do

Serve as the Single Point of Contact (SPOC) for assigned payer and Pharmacy Benefit Manager (PBM) accounts, managing stakeholder communications, issue resolution, and day-to-day contract operations.
Manage payer and PBM contracts, including pricing, membership, renewals, amendments, cancellations, and other contract lifecycle activities.
Process, validate, and reconcile Commercial, Managed Care, Trade, and Medicare Part D rebate payments in accordance with contractual requirements.
Analyze pricing, utilization, reimbursement, and financial data to identify trends, resolve discrepancies, mitigate risk, and optimize revenue performance.
Validate contract terms, rebate eligibility, and customer utilization data to ensure payment accuracy, compliance, and data integrity.
Support government pricing activities by identifying pricing inconsistencies, outdated rebate amounts, and potential compliance risks.
Manage invoice and payment timelines to ensure timely processing, reduce financial exposure, and support cash flow objectives.
Develop and maintain dashboards, KPI reporting, payment trackers, and operational analyses to support business and contracting decisions.
Partner with Market Access, Sales, Finance, Compliance, Legal, Government Pricing, and IT teams to resolve complex business challenges and improve operational performance.
Support system enhancements, User Acceptance Testing (UAT), audits, and continuous improvement initiatives that enhance efficiency, compliance, and customer experience.

Interested? For this role we’re looking for the following education, experience and skills
Minimum Experience/Skills Required:

Bachelor's degree in Finance, Business, Statistics, Healthcare Management, Economics, Marketing, or a related field.
5+ years of experience in analytics, reporting, forecasting, financial analysis, contract operations, pricing, rebates, or commercial operations.
Strong analytical skills with experience working with large and complex datasets.
Advanced Microsoft Excel skills and proficiency with PowerPoint and other Microsoft Office applications.
Experience with SAP and/or contract, pricing, or revenue management systems.
Strong communication, problem-solving, and cross-functional collaboration skills.
Experience with Model N, Revitas, Revenue Manager, Validata, or similar revenue management platforms.
Experience with rebate processing, formulary validation, reimbursement, or contract administration.

Preferred Experience/Skills:

MBA, MHA, or other advanced business or healthcare-related degree.
3+ years of pharmaceutical, biotechnology, managed care, payer, PBM, Market Access, Contracts & Pricing, or Commercial Operations experience.
Experience developing dashboards, business intelligence reporting, and performance analytics.
Experience leading process improvement, system implementations, or UAT activities.

The reasonably anticipated salary range for this position is $88,000-$115,500 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Downstream Biomanufacturing Process Expert (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

UCB is embarking on one of the most significant investments in its history through the development of a new state-of-the-art biologics manufacturing campus in Georgia, USA.

We are looking for talented, curious and ambitious individuals who want to make a lasting impact and contribute to shaping the future of biologics manufacturing at UCB.

We are looking for a Downstream Biomanufacturing Process Expert who is collaborative, proactive and innovative to join us in our Internal Manufacturing team, based at our UCB campus in Braine-l’Alleud, Belgium. UCB is embarking on one of the most significant investments in its history through the development of a new state-of-the-art biologics manufacturing campus in Georgia, USA.

About the role

This role is part of the internal manufacturing project, contributing to the design and delivery of a future-ready biologics manufacturing facility. You will play an important role in a major biopharmaceutical manufacturing project, helping bring end-user knowledge into design and delivery decisions from start to finish. You will represent manufacturing needs, translate operational requirements into practical project inputs, and help ensure the future facility is designed for safe, high-quality and efficient commercial production in a rapidly evolving project environment.

Who you’ll work with

You will be working in a team that partners closely with manufacturing colleagues, global cross-functional teams and project stakeholders to shape a new manufacturing facility in Georgia, United States. The team combines operational expertise, technical knowledge and strong collaboration to make sure manufacturing needs are understood, reflected in project decisions and aligned with future business needs working across different time zones.

What you’ll do

Represent manufacturing in project discussions and ensure operational needs are reflected in facility design, systems and ways of working.
Translate technical, process and user requirements into clear project inputs that support practical and future-ready manufacturing solutions.
Review technical documents and data to support sound decisions for purification, filtration and buffer preparation processes.
Work with manufacturing sites and cross-functional partners to gather best practices, operational insight and lessons learned.
Promote strong health, safety, environmental and quality standards in daily project decisions and deliverables.
Stay informed on industry developments and help bring new technologies and modern manufacturing approaches into the project.

Interested? For this role we’re looking for the following education, experience and skills

Degree in a relevant scientific or engineering field, or equivalent experience in biopharmaceutical manufacturing.
Experience in biopharmaceutical operations and large-scale drug substance or purification projects within the pharmaceutical industry.
Strong knowledge of mammalian biopharmaceutical production, buffer preparation, process operations and supporting digital tools and systems.
Ability to communicate clearly, write technical documentation and collaborate effectively across functions and stakeholder groups.
Experience working in regulated manufacturing environments, including inspections, audits and compliance-focused decision-making.
Willingness to adapt to project variabilities and a rapidly evolving work environment
Fluent in English; French is an advantage.
Occasional travel to the United States may be required during conceptual design and basic design phases.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

埼玉：Quality Control Staff (Saitama, Saitama, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

本ポジションは、日本国内における品質管理業務を担うローカルポジションとして、GMPおよび関連規制に基づいた試験業務の計画・実施を通じて製品品質の確保に貢献します。

また、品質システムの向上に向け、社内外のステークホルダーと連携しながら業務を推進します。

【チームについて】

品質管理部門に属し、部門長にレポートするポジションです。試験業務の中核を担いながら、チームリーダーや試験責任者としてメンバーの育成にも関与します。グローバルチームとも連携し、高い品質基準と生産性を両立した職場環境の実現を目指します。

【主な業務内容】

・品質管理に関わるGMP、承認申請書および各種規制要件を理解し、業務に適切に反映

・試験責任者またはチームリーダーとして部門業務をリードし、メンバー育成を推進

・原材料・資材のサンプリングおよび受入試験の実施

・低分子医薬品の中間製品および最終製品の理化学試験の実施

・環境モニタリング等の微生物試験

・安定性試験の計画および実施

・試験業務の計画・調整、進捗管理、および試験責任者としてのレビュー対応

・試験結果の評価および品質関連部門との連携

・試験法の移転（Method Transfer）に関する準備・受入・調整業務

・グローバルメンバーと連携した業務推進および品質システムの改善

【必要な経験スキル】

・学士号以上

・製薬企業における品質管理または分析業務経験（5年以上）

・GMPおよび関連規制に関する知識

・低分子医薬品における理化学試験の実務経験

・試験の実施から計画・管理・レビューまで対応可能な方

・英語力（会議への参加、発言ができるレベル）

【あれば尚可】

・試験責任者またはリーダー経験
・試験法移転の経験
・品質イベント対応（逸脱・改善等）の経験
・英語を用いた業務経験

【求める人物像】

・試験業務と管理業務の双方を主体的に推進できる方
・品質を重視し、正確かつ誠実に業務を遂行できる方
・周囲と連携しながら改善や業務推進ができる方

【応募方法】

本ポジションにご興味をお持ちの方は、最新の履歴書および職務経歴書を１つのファイルにマージしてエントリーを進めてください。

選考プロセスの詳細については追ってご案内いたします。

担当リクルーター：堀口

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBで働く魅力

UCBでは、単に業務をこなすのではなく、価値を創造することを大切にしています。私たちは挑戦を恐れず、協力し合い、革新を追求しながら、患者さんのために成果を出すことを目指しています。
誰もが尊重され、受け入れられ、最善を尽くせる平等な機会がある、思いやりと支援に満ちた文化が根付いています。
私たちは常に「その先」を目指し、患者さん、社員、そして地球に対して人間らしさを大切にした価値を提供しています。UCBで働くことで、自分自身の成長を実感し、自由にキャリアを築き、可能性を最大限に引き出すことができます。

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

Solutions Quality Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

To strengthen our Quality Solutions department, we are looking for a talented profile to fill the position of: Solutions Quality Lead – Braine l’Alleud, Belgium

About the role

The Solutions Quality Lead is a senior quality leader responsible for implementing quality governance and continuously evolving the nonclinical and translational quality strategy across a global portfolio of candidate programs. The role provides strategic quality leadership across nonclinical safety, quantitative clinical pharmacology, PBPK/model-informed drug development, outsourced vendor oversight, regulatory-document readiness, and inspection-defensible documentation, data, and systems practices. The Lead ensures that phase-appropriate, risk-based quality frameworks are established and maintained to enable high-quality development decisions while preserving scientific agility and regulatory credibility.

You will work with

In this role, you will work closely with various stakeholders across multiple functions. You will collaborate with Global Quality Auditing, Quality Systems & Governance, business stakeholders within Research, External Innovation and Operations and Early Clinical Development and Translational Sciences and additional transversal UCB communities. Your role will involve contributing to process improvements, ensuring alignment with UCB Policies and Procedures and regulatory requirements.

In addition, you will be mentoring quality professionals and influencing senior stakeholders across the matrix organization. The role will represent Solutions Quality in strategic portfolio discussions, significant quality-risk evaluations, regulatory and inspection preparedness activities, and decisions impacting development strategy and execution.

What you will do

Strategic Quality Leadership and Portfolio Governance

Continuously improve the non-clinical quality strategy for candidate programs; translate portfolio priorities into risk-based standards, expectations, and governance routines.
Set and implement decision-quality expectations for development teams, ensuring scientific flexibility is preserved while data integrity, regulatory credibility, and patient focus are protected.
Represent Solutions Quality in governance discussions and provide independent Quality perspective on material risks, escalations, inspection exposure, and regulatory-readiness decisions.

Non-Clinical Quality Partnership

• Direct phase- and risk-appropriate quality approaches across nonclinical safety, clinical pharmacology, and modelling activities.

• Guide teams on in translating complex scientific work into documentation, records, and controls that are regulatory-defensible and inspection-ready.

• Facilitate development teams in balancing speed, scientific flexibility, and compliance expectations from early-phase through late-phase development.

Lead and facilitate teams on the integration and appropriate use of RWE data sources in early development, ensuring alignment with scientific intent, regulatory expectations, and contribution to TPP development.

GxP and Study Oversight

• Lead and provide quality oversight and guidance for nonclinical studies, especially where GLP or regulatory requirements (may) apply, including sponsor oversight practices for outsourced studies.

• Execute quality expectations for clinical pharmacology / human pharmacology activities, including traceability of protocol-supporting records, analyses, and reports used in regulatory submissions and responses.

• Drive pragmatic, risk-based application of quality principles to translational, modelling, RWE-derived datasets, and integrated development activities that may cross traditional GxP boundaries.

Proactively identify recurring risks in study conduct, records, systems, or outsourced oversight, drive preventive improvements across non-clinical candidate programs.

Data, Documentation, and Model Governance

• Shape decision-critical models, code, datasets (including RWE datasets where applicable), reports, and related records to ensure they are maintained in a regulatory-compliant and inspection-defensible manner.

• Partner with IT and scientific teams on computerized-systems controls, validation expectations, integration points, access controls, and archival/retrievability for development and modelling systems.

• Strengthen traceability from scientific question to study/design/analysis, interpretation, development decision, and regulatory position.

Shape governance and traceability expectations of RWE data sources, including data source origin, relevance, and linkage to scientific questions and development decisions.

Vendor / CRO Quality Support

• Collaborate with Vendor Management to provide risk-based oversight of CROs, specialist vendors, and external scientific partners used for nonclinical studies, modelling activities, and other outsourced development work.

• Collaborate with Vendor Management to set quality expectations for vendor qualification, oversight plans, escalation pathways, issue trending, and readiness for inspection or audit of externally generated data and reports.

Issue Management and Continuous Improvement

• Ensure cross-functional governance of management of deviations, quality events, documentation gaps, process failures, and CAPAs with focus on patient risk, development impact, data integrity, and regulatory significance across non-clinical candidate programs.

Regulatory and Inspection Support

• Provide regulatory-ready content to teams preparing briefing books, IND-enabling content, development packages, labelling-related modelling support, and regulatory responses; i.e., quality of substantiation, traceability, and documentation, including appropriate use of RWE to support early development strategy and TPP positioning.

• Lead cross-functional inspection readiness for development activities, especially nonclinical, modelling, study oversight, and regulatory-supporting documentation.

GxP Audit Conduct & Management

Conduct audits of Study Reports, Study Phase Reports, Study Plans and Study Plan Amendments to assure the applicable OECD guidelines (when applicable), UCB SOPs and the Analytical Methods have been adhered to and that reported results accurately reflect the raw data according to UCB SOPs and associated controlled documents
As applicable, archive audit documentation per UCB SOPs; e.g., issued audit reports, supporting documentation, QAS, additional documents as expected according to UCB SOPs and associated controlled documents

Interested? For this position you’ll need the following education, experience and skills

Bachelor’s, master’s degree or an education in a relevant scientific discipline
Strong pragmatic application of GRP, GSP, and GLP, along with non-GxP quality principles across the nonclinical development lifecycle, including the governance of diverse data types such as real-world evidence (RWE), especially in toxicology, immunotoxicology, and outsourced study oversight.
Demonstrated understanding of clinical development and clinical pharmacology study support processes.
Demonstrated understanding of PBPK / PK-PD / model-informed drug development governance, including data, code, reporting, and system controls.
Demonstrated understanding of computerized systems validation, data integrity, and electronic-record controls applicable to diverse scientific data and analysis workflows.
Inspection-readiness or audit leadership experience in R&D settings.
Strong scientific literacy sufficient to engage credibly with toxicologists, immunologists, PK/PD scientists, modelers, regulatory authors, and study teams across emerging and traditional data domains.
Excellent communication skills and the ability to explain quality implications in practical, development-relevant terms.
Proven risk-based decision-making and the ability to distinguish critical quality issues from lower-risk process noise.
Excellent organizational, issue resolution, and matrix leadership skills.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

GRA Device Lead, Atlanta, GA (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Global Regulatory Affairs (GRA) Device Lead who is strategic, collaborative, and regulatory focused to join us in our Regulatory CMC & Devices team, based in our Atlanta, GA office.

About the role

The Global Regulatory Affairs Devices Lead supports regulatory strategy and submissions for marketed and development medical devices and combination products within Neurology, Immunology, and New Medicines, particularly for cell and gene therapies. The role covers device types such as drug delivery systems, IVDs, and biomarkers.

You will help develop global regulatory strategies, prepare device documentation and submission content, support timely approvals, contribute to health authority and notified body interactions, and provide regulatory input to cross-functional initiatives and business priorities.

Who you’ll work with

You’ll work closely with the GRA Device Lead and collaborate with Global Clinical Development, Global Clinical Science and Operations, Patient Supply, and Device and Primary Packaging Development. You will also partner across the internal matrix organization and engage with health authorities and notified bodies on device matters as needed for assigned projects and products.

What you’ll do

• Lead global regulatory strategy and submissions for assigned device projects/products.

• Prepare and maintain device Technical Documentation Files for regulatory clearances.

• Support Health Authority and Notified Body interactions on device matters.

• Identify required device documents and align delivery with project timelines.

• Provide lifecycle management support to maintain device regulatory compliance.

• Contribute to internal regulatory initiatives and cross-functional workstreams.

Interested? For this role we’re looking for the following education, experience and skills

Minimum Qualifications

Master’s degree
Minimum of 10 years of medical device experience in life science and/or pharma.

Preferred Qualifications

Experience with marketed and development-stage medical devices and combination products.

Knowledge of global regulatory submissions, technical documentation, and approvals.
Experience with CE Mark, Notified Body, and/or FDA regulatory processes.
Strong regulatory strategy, risk assessment, and communication skills.
Ability to influence and collaborate across cross-functional teams.
Experience with drug delivery systems, IVDs, biomarkers, or related devices.
Familiarity with neurology, immunology, or new medicines portfolios.
Experience supporting global health authority and notified body interactions.
Knowledge of lifecycle management, including product changes and improvements.
Ability to leverage regulatory intelligence to drive innovative solutions.

This position's reasonably anticipated salary range is $148,000-$195,000 annually. The actual salary offered will consider internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Non-Clinical Safety Lead - UK (Slough, Berkshire, GB)

Make your mark for patients

About the role

Lead, communicate, and execute non-clinical safety strategies aligned with clinical development goals.
Develop integrated non-clinical safety plans supporting innovative programs. Ensure timely delivery of high-quality non-clinical data and global regulatory documentation.
Represent UCB in interactions with regulatory authorities and external partners.

What you'll do

Provide non-clinical safety expertise to discovery and development projects
Define, lead, and implement non-clinical safety strategies across programs.
Partner with clinical teams to ensure robust preclinical data supports clinical trial design.
Contribute to global regulatory submissions (e.g., IBs, Briefing Books, INDs, NDA/BLAs) and interact with regulatory authorities.
Oversee the design, review, and interpretation of non-clinical studies.
Manage non-clinical safety programs, including budgets.

Interested? For this role you’ll need the following education, experience and skills

PhD in Toxicology, Pharmacology, or related discipline (or equivalent MS/DVM with experience).
5+ years in non-clinical safety (preferably in pharma or biotech).
Deep understanding of regulatory processes and regulatory toxicology.
Experience managing and forecasting non-clinical safety budgets.
Ability to produce high-quality reports and submission documents with subject matter expert support.

Preferred Qualifications:

Accredited or registered toxicologist.
Experience in gene and cell therapy and/or other novel modalities.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

MSL Immunology Poland (Warsaw, Warsaw, PL)

Make your mark for patients

We are looking for a Medical Science Liaison (MSL) Immunology, who is eager to join our Medical Team. This is a field-based role, with a primary affiliation to our Warsaw office, requiring regular travel across Poland.

About the role

The Medical Science Liaison (MSL) Immunology is a field-based Medical Affairs professional responsible for building scientific partnerships, facilitating peer-to-peer scientific exchange, and generating medical insights that support UCB's strategy and ultimately improve patient outcomes in Immunology.

Who you'll work with

You will collaborate closely with healthcare professionals, scientific experts, investigators, medical societies, and internal cross-functional colleagues across Medical Affairs, Market Access, and Commercial teams. As a trusted scientific partner, you will contribute to aligned stakeholder engagement and support the implementation of local medical strategies.

What you’ll do

· Build and maintain trusted scientific partnerships with healthcare professionals, key opinion leaders (KOLs), and other relevant healthcare stakeholders across Poland.

· Deliver high-quality scientific exchange by communicating complex medical and scientific information in a clear, balanced, and compliant manner.

· Generate, analyze, and share medical insights to help shape local medical strategy and enhance patient value.

· Represent UCB at national and international scientific congresses, medical meetings, and advisory boards, while supporting the planning and execution of medical education and stakeholder engagement activities.

· Support evidence-generation initiatives and scientific collaborations that contribute to advancing knowledge in Immunology.

· Collaborate closely with cross-functional colleagues to ensure the effective execution of medical plans and stakeholder engagement activities.

· Conduct all activities in accordance with UCB policies, industry regulations, and applicable compliance standards.

Interested? For this role we’re looking for the following education, experience and skills

· Advanced degree in Life Sciences, Pharmacy, Medicine, or a related scientific field.

· Previous experience as a Medical Science Liaison or in a Medical Affairs role within the pharmaceutical or biotechnology industry is preferred.

· Strong scientific and clinical knowledge, ideally within Immunology or related therapeutic areas.

· Proven ability to build trusted relationships with healthcare professionals and scientific experts.

· Strong collaboration, organizational, and project management skills, with the ability to work effectively in a cross-functional environment.

· Excellent communication, presentation, and stakeholder engagement skills, with the ability to translate complex scientific information into meaningful insights.

· Fluency in Polish and English.

· Willingness to travel regularly across Poland.

Please submit your CV in English.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Grants Lead (Anderlecht, Brussels, BE)

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We are looking for a Senior Medical Grants Lead who is Curious, Collaborative, and Purpose -Driven to join our Medical Grants and External Funding team, based at our UCB office.

About the role

As the Senior Grants Lead, you will serve as UCB’s global subject matter expert for medical grants and external funding, leading grant review and approval processes while driving operational excellence, governance, and continuous improvement to ensure funding decisions align with medical strategy, scientific merit, patient benefit, and compliance requirements.

Who you will work with

What you will do

Facilitate the review process of medical grant requests, ensuring decisions are based upon scientific / medical merit and safeguarding patient’s welfare

Identify and drive process and system related improvements leading to efficiencies and process excellence

Partner with internal stakeholders and external healthcare organizations.

Provide training that builds funding knowledge and confidence.

Lead, coach, and mentor funding professionals to support high-performance, care, and shared accountability.

Interested? For this role, we are looking for the following education, experience, and skills

Degree in life sciences, pharmacy, healthcare, public health, business, or related field.

Advanced degree in science, public health, business, pharmacy, or equivalent preferred.

At least eight years’ experience in grants, external funding, medical affairs, or related work.

Experience in global, matrixed organizations with cross-functional collaboration.

Knowledge of healthcare regulations, funding governance, audits, and compliance expectations.

Curious, collaborative approach with strong communication and process improvement skills.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

VIE-Regulated Bioanalyst (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

The Braine-l'Alleud site specializes in chemical synthesis, development, manufacturing, and packaging of pharmaceutical products.

More information at: www.ucb.com

Your responsibilities will include:

Contributing to regulatory bioanalysis activities supporting the development of new therapies.
Supporting the validation of bioanalytical methods (PCR, LC-MS/MS and/or LBA) in a GLP-compliant environment.
Performing routine analysis on samples from preclinical and clinical studies.
Processing, interpreting, and documenting analytical data to ensure the robustness, reliability, and compliance of results.
Participating in the continuous improvement of analytical methods and laboratory practices.
Collaborating closely with experienced scientists in a dynamic, innovative, and regulated environment.
Ensuring adherence to quality procedures and regulatory requirements throughout all laboratory activities.

Your profile:

Hold at least a Bachelor’s degree in a relevant scientific field.
Demonstrate hands-on experience in PCR (required).
Experience in mass spectrometry (LC-MS/MS) and/or immunoassays (LBA) is considered an asset.
Additional experience with other laboratory techniques is a plus.
Ability to work autonomously in performing validation activities and routine analyses.
Strong skills in analytical data interpretation, with a focus on ensuring the reliability and robustness of developed methods.
Demonstrate organization, accuracy, and a strong sense of responsibility in a regulated environment.
Good command of English, both written and spoken.

Please note that the strict eligibility conditions for this program are as follows:

Be between 18 and 28 years old;
Hold the nationality of a member country of the European Economic Area;
Have not worked or lived in the country where the mission will take place;
Be available to dedicate yourself to the mission full-time;
If you have French nationality or dual nationality, be in compliance with the national service obligations of France (Numéro Identifiant Défense);
Have a clean criminal record.

If you do not meet all of these conditions, we will not be able to consider your application.

Principal Statistical Methodologist (UK) (Slough, Berkshire, GB)

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We are looking for a Principal Statistical Methodologist who is curious, collaborative, and strategic to join our Statistical Innovation team within Biometric and Data Sciences (BDS), based in any of our Braine l'Alleud (Belgium), Monheim (Germany), Slough (UK) or Raleigh (US) offices.

About the role

You will help shape how evidence is generated, modeled, and communicated across the drug development lifecycle, bringing modern computational and machine-learning methods to bear on real R&D decisions. You will develop and apply advanced data-driven and model-based approaches—drawing on statistics, machine learning, and AI—translate them into robust, reusable tools, and partner across functions to put them to work where they impact drug development decision making. You will also contribute to the group's scientific profile through publications and external collaboration.

Who you will work with

You will be working in a team that provides statistical consultancy across therapy areas and development stages, partnering closely with colleagues in clinical development, regulatory strategy, data science, and medical affairs. The team values curiosity and problem solving, practical innovation, clear communication, and collaboration, bringing novel quantitative and computational approaches into real study decisions and sharing learnings with the wider scientific community.

What you will do

Develop and apply advanced computational and statistical methods, including machine learning, AI, and scenario evaluation using modern simulation approaches, to inform design, analysis, and decision-making across development.
Build robust, well-engineered, reusable tools and workflows that bring these methods into routine use, with attention to reproducibility and software quality.
Bring a quantitative lens with appropriate rigor to emerging problems such as synthetic and external control data, causal inference, and digital-twin or simulation-based approaches.
Partner with statisticians and cross-functional colleagues to identify where computational and data-driven methods add the most leverage, and translate complex approaches into clear insight for technical and non-technical audiences.
Contribute to internal capability building by sharing tools, code, and methods across the team and wider organization.
Contribute to the group's external profile through scientific publications, conference presentations, and participation in cross-industry initiatives and working groups.

Interested? Here is what we are looking for

Doctoral degree in statistics, biostatistics, mathematics, computer science with a strong quantitative/statistical component, or a closely related discipline with a solid grounding in statistical inference and uncertainty.
3+ years of experience within the pharmaceutical industry. Experience in advanced computational methodology for clinical development (early to late stage) is an advantage. Direct entry may be considered.
Strong, multi-language scientific programming skills (R and Python preferred; software-engineering practices such as version control, testing, and reproducible workflows a clear advantage).
Demonstrated expertise in machine learning and/or AI methods, with hands-on experience applying them to real problems; experience with large language models, causal inference, synthetic data, or digital-twin/simulation approaches is a strong advantage.
Sound knowledge of ICH guidelines and understanding of regulatory requirements from major health authorities.
Ability to work effectively with autonomy, manage multiple priorities, and deliver timely, high-quality outputs.
Clear written and spoken communication in English, including the ability to explain technical concepts to non-technical audiences.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?

At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

IC Business Partner (Atlanta, Georgia, US)

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About the role:

We are looking for a highly analytical and strategically minded Incentive Compensation (IC) Business Partner to support our Field & Sales Incentive Compensation team in the Ecosystems Operations Function. This role sits at the intersection of data, strategy, and operations providing critical analytical support, actionable insights, and governance to ensure effective design, execution, and monitoring of incentive compensation programs.

Who you’ll work with:

Field & Sales Incentive Compensation team in the Ecosystems Operations Function

What you’ll do:

The ideal candidate brings strong data modelling capabilities, a structured problem-solving approach, and the ability to translate complex data into clear business recommendations. This role also serves as a key liaison between Incentive Compensation, Sales Operations, CRM, and data management teams, with the flexibility to support adjacent functions such as roster and alignment when needed.

Incentive Compensation Strategy & Analytics

1. Provide analytical support for IC plan design, scenario modeling, and performance forecasting
2. Translate business objectives into measurable compensation structures and KPIs
3. Conduct advanced modeling to assess plan effectiveness, risk, and financial impact
4. Deliver strategic insights and recommendations based on performance trends and field behavior

Plan Design, Monitoring & Health Checks

1. Support IC plan design and contest design with robust analytics and benchmarking
2. Develop and execute ongoing health check analytics to evaluate plan performance
3. Monitor plan outcomes and recommend adjustments to optimize effectiveness
4. Identify outliers, risks, and unintended consequences through data analysis

Data Management & Quality Assurance

1. Act as the primary conduit between Incentive Compensation and data/IT teams
2. Ensure integrity, accuracy, and completeness of all IC-related data sources
3. Perform rigorous QC/validation of data inputs and payroll outputs
4. Support payroll file validation to ensure accurate and timely compensation payouts

Cross-Functional Partnership

1. Collaborate closely with Sales Operations, CRM, and Roster & Alignment teams
2. Provide analytical support that is transferable across Ecosystem Operations functions
3. Translate data into actionable insights for non-technical stakeholders
4. Support ad hoc business analyses and leadership requests

Vendor Management & Governance

1. Manage relationships with external IC vendors and data partners
2. Oversee vendor deliverables, timelines, and service quality

Interested? For this role we’re looking for the following education, experience and skills:

Required Qualifications:

Bachelor’s degree in business, Finance, Economics, Pharmaceutical Marketing, or related field
* Masters Degree Required
* 2–4 years of experience in sales analytics, reporting, forecasting, or Incentive compensation

Preferred Qualifications:

1–2 years of experience in pharmaceutical or consulting environments preferred
Strong expertise in data modeling, advanced analytics, and quantitative problem-solving
MBA or advanced degree preferred

This positions reasonably anticipated base salary range is $108,000 to $141,800 per year. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Braine Procurement P2P Manager (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Braine Procurement P2P Manager who is impact-driven, resilient, and collaborative to join our team in Braine Supply Chain, based at our UCB campus located in Braine-l’Alleud, Belgium.

About the role:

You will play a key role in ensuring the availability of critical raw materials and components that keep our operations running smoothly. You will translate global procurement strategies into local execution and safeguard production continuity by managing supply risks. You are going to lead procurement performance on site, drive operational excellence, and strengthen supply chain resilience in a fast-evolving environment.

Who you will work with:

You will work closely with the local Procurement team and collaborate daily with Planning, Production, Quality, Warehouse, Finance and Global Procurement to ensure materials and services are available to support site operations.

You will also maintain strong relationships with suppliers to resolve operational issues, improve supplier performance and support the site’s day-to-day procurement activities.

What you will do:

Lead the day-to-day operational Procurement and Procure-to-Pay (P2P) activities for the Braine site.
Manage and develop the local Procurement team, ensuring efficient execution and high service levels.
Ensure the continuous availability of materials and proactively resolve supply issues to support uninterrupted production.
Collaborate closely with Planning, Production, Quality, Warehouse, Finance and Global Procurement to support site operations.
Build and maintain strong relationships with suppliers to ensure reliable deliveries and operational performance.
Monitor operational KPIs such as OTIF, inventory levels and lead times, and implement improvements where needed.
Identify opportunities to simplify processes, improve supplier performance and enhance the efficiency of Procurement operations.

Interested? For this role, we are looking for the following education, experience, and skills:

You have a degree in supply chain, procurement, engineering, or a related field.
You bring strong procurement experience in pharmaceutical or chemical industry environments.
You demonstrate solid knowledge of global procurement processes and supplier management.
You are comfortable using ERP systems and planning tools for decision-making.
You show strong leadership, decision-making, and problem-solving skills under pressure.
You excel in cross-functional collaboration, negotiation, and continuous improvement initiatives.
Bilingual proficiency in English and French, both written and verbal.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Outcomes Liaison, Central (Birmingham, Alabama, US)

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Candidates must reside within the territory and live near a hub airport in the territory.

Up to 75% of travel required, including overnights and some weekends.

About the Role

What You’ll Do

Lead execution of the Epilepsy & Rare Syndromes outcomes and RWE engagement strategy across key accounts.
Build and maintain relationships with C‑suite stakeholders, researchers, and payer decision‑makers.
Identify and develop institutional data opportunities that align with strategic evidence needs.
Support field‑based research collaborations and HEOR data generation.
Serve as an expert communicator delivering clinical and economic value propositions across settings of care.
Partner cross‑functionally to address clinical and HEOR data needs at key accounts.

Who you’ll work with

Senior healthcare leaders, including C‑suite and D‑suite decision‑makers within large medical groups, to support high‑level strategic engagements.
Top‑tier research institutions to advance scientific and outcomes‑focused initiatives.
Pharmacy and medical directors at regional payers, providing clinical and economic insights that inform access and value discussions.
Integrated delivery networks (IDNs) and large medical groups to drive outcomes‑ and RWE‑aligned strategies.
Internal cross‑functional partners—regional business units, marketing, sales, medical affairs, and corporate functions—to ensure coordinated execution across the organization.

Interested? For this role we’re looking for the following education, experience, and skills

Minimum Qualifications

Clinically focused graduate degree (MPH, NP, PA). Doctorate degree (PharmD, MD, DO, PhD, DNP) preferred.
Doctoral candidates: Minimum 8 years industry experience + 3 years HEOR/RWE/Outcomes experience.
Non‑doctoral candidates: Minimum 10 years industry experience + 5 years HEOR/RWE/Outcomes experience.

Preferred Qualifications

Doctorate preferred (PharmD, MD, DO, PhD); non‑doctoral clinicians considered with relevant expertise.
Strong background in external stakeholder engagement and decisionmaker relationship management.
Ability to analyze clinical and HEOR data gaps and deliver meaningful solutions.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Bio Process Engineer Senior (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a talented and motivated  Senior Bio Process Engineer to join our Belgium Biomanufacturing Operations Center in Braine-L’Alleud, Belgium.

About the role :

You will play a key role in delivering complex projects within a state-of-the-art biopharmaceutical manufacturing environment. You will lead process and equipment improvement initiatives, solve technical challenges across manufacturing, engineering, automation and digital systems, and contribute to operational excellence.

Who you’ll work with :

You will be working in a multidisciplinary team that partners closely with manufacturing, engineering, automation, digital technology, quality, and external suppliers. Together, you will support critical manufacturing operations, deliver strategic improvement projects, and solve complex technical challenges that contribute to the production of innovative medicines. The team values collaboration, continuous learning, and a shared commitment to excellence.

What you’ll do :

Lead complex process and equipment improvement projects from planning through execution and implementation.

Develop project plans, budgets, timelines, resource strategies, and risk mitigation actions.

Collaborate with internal stakeholders and external partners to ensure successful project delivery.

Investigate and resolve complex manufacturing, engineering, and automation-related issues.

Conduct root cause investigations and implement corrective and preventive actions to improve operational performance.

Support production activities and contribute to continuous improvement and operational excellence initiatives.

Interested ? For this role we’re looking for the following education, experience and skills :

Bachelor’s or Master’s degree in Engineering, Biotechnology, Bioprocessing, or a related scientific field.

Strong knowledge of biomanufacturing processes, process optimization, and regulated manufacturing environments.

Significant experience in engineering and/or automation and/or operation and/or manufacturing science and technology

Proven project management experience, including planning, risk management, stakeholder engagement, and project execution.

Experience troubleshooting complex technical challenges and implementing sustainable solutions.

Fluent communication skills in English and French.

#Biomanufacturing

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Account Specialist HS - Charlotte (Charlotte, North Carolina, US)

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To strengthen our New Hidradenitis Suppurativa Dermatology Sales Team, we are looking for a talented individual to join our team in the position of: Clinical Account Specialist HS in Charlotte, NC.

The Clinical Account Specialist (CAS) position is responsible for driving demand for the current and future Dermatology pipeline assets in an assigned territory. Reinforcing the clinical features of the product, engaging and building relationships with clinical decision makers and office support staff, and working in concert with the broader UCB organization to create the best experiences for patients living with severe immunologic diseases.

About the role:

Develop a strong understanding and awareness of the patient journey of care, including taking responsibility for ensuring needed therapies get to the patient.
Offer an outstanding patient experience with our product by communicating clinical information on dermatology products and relevant patient support services to an audience of health care professionals and office staff.
Establish an understanding of the local health care ecosystems, including the payor environment.
Demonstrate the UCB Patient Value Strategy principles by establishing collaborative and team-oriented working relationships and integrating within a matrix environment.
Behave compliantly with all UCB policies / approved messages and coach the team to use of approved UCB sales materials and messages with HCPs and other external stakeholders.

What you’ll do:

Owning responsibility for attaining territory sales goals and objectives through effective territory planning, visiting clinical decision makers with appropriate reach/frequency, collaborating with the Immunology Clinical Specialist and other members of the UCB Patient Value Team.
Analyzing territory data to build and adapt a customer call plan to establish professional working relationships with HCP and support staff.
Maintaining a thorough understanding of the competitive marketplace and drivers of prescriber decisions.
Conducting account related activities such as profiling, call planning, and reviewing UCB sales data with assigned stakeholders.
Making strategic business decisions in the management of allocated resources such as financial/budgets, samples, access opportunities.
Coordinating and supporting promotional educational opportunities and programs intended to expand the knowledge of medical stakeholders and staff (e.g., peer-to-peer educational opportunities) in accordance with UCB policy.

Interested? For this position you’ll need the following education, experience and skills:

Minimum Qualifications:

Bachelor’s Degree BA/BS
Minimum of 3 years of direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry
Must have a valid Driver License with no more than 2 moving violations in the previous three-year period
Must reside within assigned geography

Preferred Qualifications:

5 years of direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry

Experience calling on Dermatologists in the assigned geography
Experience selling injectable biologics products
Proven track record of success in Pharmaceutical Sales demonstrated by goal attainment and awards achievement (President’s Club, etc.)
Biologic product launch experience
Demonstrated business and strategic planning skills to identify unique selling opportunities and adaptability to changing market conditions
Demonstrated understanding of managed care landscape and how it influences/impacts business
Strong verbal, influencing, presentation and written communication skills
Strong collaboration skills and success working in teams

This positions reasonably anticipated base salary range is $132,000 to $174,000 per year. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Scientist - Neuroinflammation (In Vivo) (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Senior Scientist – Neuroinflammation (In Vivo) who is passionate, collaborative and driven to join us in our Neuroinflammation Research team, based in our UCB Pharma office in Braine-l’Alleud, Belgium.

About the role

You will contribute to the development of innovative therapies by designing and executing in vivo studies in neuroinflammation. Working at the bench, you will generate high-quality data to support target identification, validation and early development programs. This role is ideal for someone who enjoys hands-on laboratory work and wants to make a direct impact on drug discovery.

Who you’ll work with

You will be working in a team that focuses on neuroinflammation and neuroimmune diseases, within a collaborative and multidisciplinary research environment. You will partner with internal experts across biology, pathology and drug discovery, as well as external scientific partners, to advance research programs and deliver meaningful outcomes for patients.

What you’ll do

Design and execute in vivo studies in neurological disease models
Perform dosing, surgery, behavioral testing and tissue collection
Generate and analyze data using imaging and molecular techniques
Apply in vitro and ex vivo approaches to support experiments
Collaborate with internal teams and external research partners
Contribute to ethical processes and animal welfare standards

Interested? For this role we’re looking for the following education, experience and skills

Doctoral degree in neuroscience, immunology, or related field. Postdoctoral experience is preferred. Strong background in the field of neuroinflammation
Experience studying how the peripheral immune system contributes to autoimmune, autoinflammatory and degenerative neurological diseases
Exceptional hands-on experience with in vivo rodent models of neurological disease, FELASA C certification or equivalent is required
Knowledge of neuroinflammation and immune mechanisms in neurological diseases. Experience running experimental autoimmune encephalomyelitis/neuritis (EAE/EAN) or similar is beneficial
Experience in drug discovery within industry or biotechnology preferred
Passionate, strong communication skills with collaborative and proactive mindset
Fluent in English, additional languages are an advantage

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Contremaître Thermique (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

À propos du rôle

Avec qui vous allez collaborer

Ce que vous allez faire

Vous allez coordonner, planifier et réaliser les activités de vérification, calibrations et ajustements des équipements.
Vous serez responsable de la gestion des plannings à court et moyen terme selon les contraintes opérationnelles.
Vous encadrerez et accompagnerez les équipes techniques et les nouveaux collaborateurs.
Vous apporterez un support technique et participerez activement aux activités de dépannage.
Vous assurerez le respect des normes GMP, qualité et sécurité dans toutes les interventions.
Vous gérerez la documentation, les rapports et les mises à jour dans SAP et Optimu (logiciel de métrologie).

Intéressé.e ?

Pour ce rôle, nous recherchons les compétences et qualifications suivantes

Bachelier en électromécanique ou expérience technique équivalente.
Expérience en environnement technique ou de production, idéalement en industrie réglementée.
Excellente organisation et capacité à prioriser de manière autonome.
Aisance relationnelle avec de multiples parties prenantes.
Flexibilité et capacité d’adaptation à un environnement dynamique.
Connaissances de base en anglais ; expérience SAP et environnement GMP sont des atouts.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

IT & Digital Procurement Category Manager (Anderlecht, Brussels, BE)

Make your mark for patients

About the Role

Who You’ll Work With

What You’ll Do

Manage a global Technology spend and oversee end-to-end technology procurement processes.
Develop and implement technology category strategies to drive proactive spend management.
Identify opportunities to optimize technology spend and enhance supplier value.
Build and maintain strong relationships with internal stakeholders and strategic suppliers.
Identify potential suppliers and lead supplier selection efforts.
Manage complex RFI/RFP processes using procurement-approved tools.
Provide fact-based sourcing recommendations considering market dynamics and competitive trends.
Negotiate commercial terms and ensure contractual compliance in partnership with Legal.
Embed risk management and sustainability requirements into supplier contracts.
Support continuous improvement initiatives and approve POs within defined thresholds.

Interested? For this role we’re looking for:

Minimum 8 years’ experience in strategic procurement, sales, or digital technology roles.
Strong negotiation and supplier management experience, especially within technology domains.
Excellent communication, stakeholder engagement, and leadership skills.
Deep understanding of the IT/Digital landscape, with curiosity and adaptability in a dynamic environment.
Team-oriented, collaborative mindset with commitment to diversity and inclusion.
Fluent in English.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Bio Process Subject Matter Expert (SME) (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Bio Process Subject Matter Expert (SME) who is strategic, collaborative, and solution-oriented to join our Global Engineering and Biopharmaceutical Development team, based at our UCB campus located in Braine-l’Alleud, Walloon Brabant, Belgium.

About the role

As a Bio Process SME, you will be at the heart of our global engineering and biopharmaceutical development ecosystem. You will help shape the technical vision and lifecycle strategy for biopharmaceutical processes, from development to industrial-scale manufacturing. You will ensure our process solutions are robust, scalable, compliant, and future-ready across development, scale-up, technology transfer, and commercial production.

Who you will work with

You will work closely with Engineering, MSAT, Process Development, Operations, Quality, Validation, and external partners. You will act as a strategic technical partner across sites and projects, helping teams align process requirements with engineering design, compliance expectations, and manufacturing needs. You will also contribute to knowledge sharing, standardization, and the adoption of new technologies.

What you will do

• You will define process strategies, standards, and best practices for USP, DSP, filtration, viral clearance, CIP and SIP.
• You will support CAPEX projects from feasibility through commissioning, qualification, and process performance qualification.
• You will translate process needs into URS, design inputs, PFDs, mass balances, and critical process parameters.
• You will lead or support process scale-up, industrialization, and technology transfers across sites or external partners.
• You will ensure alignment with GxP, GMP, FDA, EMA, validation, and quality-by-design expectations.
• You will analyze process performance, support troubleshooting, and drive continuous improvement in robustness, yield, and efficiency.

Interested? For this role, we are looking for the following education, experience, and skills:

• You have a degree in Biotechnology, Biochemical Engineering, Chemical Engineering, or an equivalent scientific field.
• You bring significant experience in biopharmaceutical process development, manufacturing, scale-up, or industrialization.
• You have strong expertise in USP and/or DSP processes and bio-process equipment.
• You understand GMP, GxP, qualification, validation, PPQ, CPV, and process robustness principles.
• You are confident using data analysis, process modeling, statistical tools, and risk assessment methods.
• You communicate clearly, influence across functions, and turn complex technical topics into pragmatic solutions.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Manager Biomanufacturing - Upstream (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a talented and motivated Biomanufacturing Manager - Upstream to join our Belgium Biomanufacturing Operations Center in Braine-L’Alleud, Belgium.

About the role :

You will be responsible for overseeing manufacturing operations within a biopharmaceutical production environment. You will ensure production runs efficiently, safely, and in compliance with regulatory standards while fostering continuous improvement and team development. You will play a key role in delivering production targets, maintaining quality standards, and building a strong, engaged team.

Who you’ll work with :

You will be working in a team that collaborates closely with production teams, quality specialists, supply chain, technical services, and human resources. You will lead team leaders and technicians while partnering with cross-functional experts to ensure smooth, compliant, and efficient manufacturing operations.

What you’ll do :

Ensure safe, compliant, and efficient execution of manufacturing operations aligned with quality, safety, and production targets
Lead and support team leaders and technicians, promoting collaboration, development, and continuous improvement
Monitor production performance, analyze results, and implement corrective actions when needed
Oversee equipment readiness with technical teams, including maintenance, qualification, and calibration
Manage deviations, investigations, and corrective actions to ensure regulatory compliance
Drive continuous improvement initiatives and support audits and inspections

Interested ? For this role we’re looking for the following education, experience and skills :

Bachelor’s or Master’s degree in science, engineering, or related field
Proven experience (10+ years) in biopharmaceutical manufacturing
Experience in leading production teams in a regulated environment (including executive-level staff), high leadership skills
Strong knowledge of Good Manufacturing Practices, industrial production processes and technologies, included upstream processes
Strong communication, problem-solving, and decision-making skills
Ability to work in highly dynamic environment and to handle challenging situations
Fluent in French and English

#Biomanufacturing

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

VIE Digital Innovation Analyst (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

The Braine-l'Alleud site specializes in chemical synthesis, development, manufacturing, and packaging of pharmaceutical products.

More information at: www.ucb.com 

Your role

You will contribute to identifying, testing, and implementing innovative digital solutions to improve ways of working, with a strong focus on manufacturing and supply chain activities to ensure the availability of medicines for patients.

Working closely with both business and IT teams, you will help translate operational needs into concrete, high-value use cases that can be tested, validated, and scaled. This role is part of a broader digital transformation effort aiming to improve operational performance. The focus rests on better visibility on operations, more efficient and reliable processes, faster, data-driven decision-making and adoption of impactful digital solutions.

What you will do

In this role, you will be involved in projets end‑to‑end, from idea exploration to the implementation of solutions. You will:

Understand operational challenges and define relevant digital use cases
Explore and assess solutions using technologies such as advanced analytics, generative AI and digital twins
Contribute actively to feasibility studies and innovation initiatives

During experimentation phases, you will stay hands-on by working on analyses, prototypes or dashboards, while gathering user feedback to refine solutions. As projects mature, you will progressively move toward a more structured Business Analyst role, supporting:

Requirement definition and documentation
Alignment between business and technical stakeholders
Preparation for scaling and industrialization of selected solutions

Your profile:

- Master’s degree in engineering, AI, data science, computer science, information systems, analytics, or a related field
- Fluent in English (required); French is a plus
- Good understanding of data, advanced analytics, and innovative digital technologies
- Strong interest in artificial intelligence (including generative AI), as well as modeling and digital twins
- Ability to structure business problems, analyze user needs, and propose pragmatic solutions
- Comfortable working in a cross-functional, international, and evolving environment
- Demonstrates initiative, curiosity, analytical rigor, and strong communication skills

Be between 18 and 28 years old;

Hold the nationality of a member country of the European Economic Area;

Have not worked or lived in the country where the mission will take place;

Be available to dedicate yourself to the mission full-time;

If you have French nationality or dual nationality, be in compliance with the national service obligations of France (Numéro Identifiant Défense);

Have a clean criminal record.

If you do not meet all these conditions, we will not be able to consider your application.

Senior Real World Evidence Expert (Belgium) (Anderlecht, Brussels, BE)

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We are looking for a Senior Real World Evidence Expert who is scientifically rigorous, strategically minded, and passionate about generating impactful real‑world evidence to help shape key decisions across the lifecycle of UCB’s assets, based in Slough, UK or Brussels, Belgium

About the Role

As a Senior RWE Expert, you will autonomously design, lead, and deliver a wide range of global real‑world evidence (RWE) studies. Your work will inform internal decision-making, support regulatory and payer interactions, and contribute to the scientific understanding of disease areas. In addition to overseeing project delivery, you will help shape asset‑level RWE strategies and propose innovative approaches to evidence generation in partnership with the RWE Strategy Lead.

Who You’ll Work With

You will collaborate with statistical teams, RWE Analysts, epidemiologists, clinical teams, Evidence Synthesis partners (HE/HTA), Safety/Pharmacovigilance, external vendors, medical experts, and cross‑functional asset teams. You will serve as an influential scientific contributor with the ability to engage diverse stakeholders and ensure RWE outputs meet strategic, regulatory, and scientific needs.

What You’ll Do

Lead execution of complex global RWE studies using diverse methodologies and datasets end‑to‑end.
Develop study concepts, write protocols, shape analysis plans, and ensure governance and QC compliance.
Deliver epidemiology, natural‑history, burden‑of‑disease, safety‑outcome, regulatory, and comparative‑effectiveness studies.
Represent RWE on primary data‑collection teams and lead high‑visibility secondary data‑use initiatives.
Collaborate with vendors, clinicians, statisticians, and analytics teams to deliver scientifically robust outputs.
Interpret results and communicate findings internally and externally across scientific and strategic forums.
Co‑define evidence needs with HE/HTA partners, Safety, and other functions to support regulatory and payer interactions.
Contribute to asset‑level RWE strategy and propose innovative study designs, data sources, and analytic approaches.
Advocate for rigorous scientific methodology and challenge assumptions using strong methodological reasoning.
Help advance RWE functional excellence through thought leadership, innovation, and best‑practice sharing.

Interested? For this role we’re looking for:

Master’s degree, PhD, or MD in a life science, epidemiology, outcomes research, HEOR, statistics, or related field.
Experience designing and delivering RWE studies using primary or secondary data in pharma, academia, or consultancies.
Strong quantitative and methodological expertise across epidemiology, pharmacoepidemiology, and outcomes research.
Ability to develop high‑quality scientific communications (abstracts, manuscripts, posters, presentations).
Excellent communication skills with the ability to influence and engage cross‑functional and senior stakeholders.
Proven ability to lead projects independently, think strategically, innovate, and adapt in fast‑changing environments.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Team Leader Maintenance Week-end (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Team Leader Maintenance Week-end qui est proactif·ve, orienté·e personnes et orienté·e résultats pour rejoindre notre équipe BelTech Maintenance – Pôle Bio, basée sur notre campus UCB situé à Braine-l’Alleud, Brabant Wallon, Belgique.

À propos du rôle

En tant que Team Leader Maintenance, vous allez jouer un rôle clé dans la performance de nos équipements de production. Vous allez garantir leur disponibilité optimale en coordonnant les activités de maintenance et en encadrant les équipes techniques. Vous vous assurez que les opérations respectent les standards GMP, de sécurité et de qualité, tout en contribuant activement à l’amélioration continue et aux projets techniques du site.

Le poste est basé sur un horaire de journée : 8h00 – 16h30, du samedi au lundi.

Avec qui vous allez travailler

Vous allez collaborer étroitement avec les équipes Maintenance, Production, Engineering, HSE et Qualité. Vous allez également interagir avec des partenaires externes et des sous-traitants. Vous travaillez en lien direct avec votre responsable et vous contribuez à créer un environnement collaboratif, dynamique et orienté performance au sein des Services Techniques.

Ce que vous allez faire

Vous allez encadrer une équipe technique et coordonner les activités de maintenance des équipements de production
Vous serez responsable de garantir la planification et l’exécution des maintenances préventives et correctives
Vous allez gérer les priorités opérationnelles et assurer le suivi des interventions et des indicateurs de performance
Vous allez garantir la conformité GMP, sécurité (HSE) et qualité dans toutes les activités de maintenance
Vous allez piloter l’amélioration continue, la fiabilité des équipements et l’approche « zéro panne »
Vous allez collaborer avec les équipes internes et partenaires externes afin de soutenir les projets techniques

Intéressé·e ?

Pour ce rôle, nous recherchons les qualifications, l’expérience et les compétences suivantes :

Diplôme technique ou expérience équivalente avec une expertise solide en maintenance industrielle
Expérience en gestion d’équipe ou rôle de leadership technique
Bonne connaissance des environnements réglementés et des normes GMP (expérience dans le milieu pharmaceutique obligatoire)
Capacité à prendre des décisions de manière autonome et à gérer les priorités
Excellentes compétences en communication en français et en anglais technique
Esprit analytique, orientation résultats et capacité à résoudre des problèmes complexes

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

New Product Planning Team Lead (Anderlecht, Brussels, BE)

Make your mark for patients

We are looking for a New Product Planning Team Lead – Immunology who is strategic, collaborative, and insight‑driven to join us in our New Product Planning (NPP) team, ideally based at our HQ in Brussels. We can also consider, Slough, UK (Windlesham, Surrey 2027), or Boston, US.

About the role

New Product Planning (NPP) is the early commercial strategy function that brings patient, physician, payer, regulatory, competitive, and market perspectives into pipeline and development decisions.

As an NPP Team Lead, you will play a critical role in shaping asset strategy to maximize long-term value, differentiation, and growth. Operating at the interface with Patient Evidence, you will help deliver de-risked Immunology assets with strong potential to generate value for patients, society, and UCB.

Who you’ll work with

You will act as the early commercial strategy partner to Candidate teams (ie. teams accountable for assets under Patient Solutions leadership) ensuring early development choices are informed by future market opportunities, stakeholder needs, competitive dynamics, and scenario-based trade-offs.

You will therefore collaborate closely with cross-functional stakeholders across research, clinical, CMC, access & price, medical, regulatory and insights.

You will report to the Head of New Product Planning and lead a team of NPP Leads, fostering a high-performing, inclusive, and collaborative environment.

What you’ll do

You will define the key drivers of success for future assets and lead resolution of critical commercial and stakeholder questions
Shape asset maximization strategies, including indication selection and sequencing and long-term value creation scenarios

Translate patient, physician, payer, regulatory, and competitive insights into indication strategy, Target Product Profiles, business cases, and proof-of-concept commercial success criteria
You will identify early evidence needs and key gaps to strengthen development readiness and progression
Lead, coach, and develop a team of NPP Leads, building capability and a high-performing team culture

Interested? For this role we’re looking for the following education, experience and skills

Advanced degree in life sciences, business, or a related field

Significant (10+ years) global experience in evaluating early pipeline assets and shaping early commercial strategy: experience in New Product Planning or related strategic roles, with a strong track record of linking development choices to future commercial value
Ability to understand biology and mechanisms of action and connect to potential for patient value creation
Ability to shape strategy using insights, scenario planning, and long-term value focus
Strong influencing, stakeholder management, and cross-functional collaboration skills
You communicate clearly and confidently, tailoring insights and recommendations to audiences including senior decision-makers
You lead with authenticity, integrity, respect, and have strong relationship-building capability
You demonstrate curiosity, learning agility, and a forward-looking mindset
You build an inclusive and open team culture where diverse perspectives are encouraged and valued
Proven people leadership with the ability to coach, develop, and inspire high-performing teams

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Digital Technology Enterprise Architect (Anderlecht, Brussels, BE)

Make your mark for patients

We are looking for a passionate Digital Technology Enterprise Architect who is a strong connector-communicator with an innovative and inquisitive mindset to join our DT Strategy & Architecture team, based in our Brussels (Anderlecht) office, Belgium.

About the role

As a Digital Technology Strategy– Enterprise Architect, you develop, drive adoption of and ensure the effectiveness of our technology strategy and architecture in delivering impactful business outcomes and patient value, with future flexibility and adaptability in mind. You are a trusted advisor with a hands-on attitude, and thrive on collaboratively solving complex challenges and architecting innovative solutions. You have a passion for new technologies and trends, and the business opportunities they offer. You enjoy working in an agile, iterative, and outcome-focused environment, exemplified by a user experience centric and product management mindset.

Team

You will work within a team of highly skilled architects. You will partner with key stakeholders across the company and ecosystem to acquire a deep understanding of the business needs, opportunities, challenges and ecosystem factors in order to develop, propose and promote the adoption of timely, relevant and impactful IT technology strategies and solutions. You will tackle leading-edge challenges in collaboration with multidisciplinary internal and external experts we have privileged access to thanks to our partnerships.

What you’ll do

Apply and grow your technology strategy and architecture expertise, crafting impactful stakeholder solutions across the digital spectrum.
Provide guidance on emerging technologies and trends, and strategic digital initiatives; develop points-of-view and formulate decision-ready recommendations.
Co-create enterprise and domain level technology strategies and roadmaps with colleagues and partners, communicate and champion their implementation.
Co-create actionable architectural designs and recommend technology, vendor and delivery options, informed by proactively engaging and advising stakeholders on vision and roadmaps, functional and operational requirements, goals and constraints. You facilitate decision making by clearly articulating options and trade-offs, and pragmatically applying well-architected principles and frameworks, aiming for resilience and agility.
Co-create and evangelize reusable methodologies, reference architectures, patterns and other artefacts to accelerate time-to-market for new systems, while reducing cost and/or risk.
Foster a culture of innovation across the organization, while driving continuous improvements, internalizing and scaling learnings and best practices.

Interested? For this role we’re looking for the following education, experience and skills

A master’s degree in Computer Sciences, (Business) Engineering or a related degree. And at least 3 years of experience in the analysis, design, development, and deployment of technology solutions, adopting an enterprise perspective.
Practical knowledge on modern architectural styles, patterns, and practices. Experience with cloud (native) architectures and well-architected frameworks, including security.
Good understanding of product management, agile principles, and development methodologies.
An analytical approach and attitude, using data and facts to support strategic recommendations.
Strong business acumen, communication, negotiation and influencing skills. Fluent command of English is a must, other languages are a plus.
Passion for working in multidisciplinary teams, embracing different perspectives to drive better outcomes. Able to inspire and rally commitment for novel ideas and approaches.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Automation Development scientist (Slough, Berkshire, GB)

Make your mark for patients

We are looking for an Automation Development Scientist who is innovative, collaborative and detail-oriented to join our Characterisation and Material Sciences team, based in our Slough office in the United Kingdom.

About the role

You will support the development and implementation of automated solutions to enhance scientific workflows. Working across multiple projects, you will design and optimise processes that improve efficiency, data quality, and reproducibility. This role plays a key part in advancing innovative approaches aligned with future laboratory strategies while collaborating with diverse stakeholders across research and development.

Who you’ll work with

You will be working in a team of experienced scientists focused on the characterisation of molecules and materials. The team collaborates closely with experts in formulation, analytical development, digital and technology, and quality. You will also interact with international colleagues and external partners, contributing to a highly collaborative and multidisciplinary environment.

What you’ll do

Develop and implement automation solutions to support molecule characterisation and improve laboratory workflows.
Collaborate with scientists and digital teams to translate technical needs into practical automated solutions.
Design studies, and create and review protocols and reports to support project objectives.
Improve efficiency, data accuracy, and overall capability while reducing manual work and resource use.
Contribute to project planning and optimisation of scientific work packages.
Ensure compliance with quality standards and contribute to continuous improvement initiatives.

Interested? For this role we’re looking for the following education, experience and skills

Master’s or PhD in a scientific field such as biotechnology, chemistry, or a related discipline, with relevant experience.
Experience in pharmaceutical or biotechnology analysis environments.
Knowledge or experience with automation technologies and scientific workflows.
Strong communication skills with the ability to collaborate across teams.
Ability to manage multiple priorities and adapt to changing project needs.
Proactive mindset with attention to detail and a willingness to learn.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien.ne de maintenance Utilities (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un/e Technicien/e de maintenance Utilities qui est minutieux/se, proactif/ve et collaboratif/ve pour nous rejoindre sur notre campus de Braine-l'Alleud, Belgique.

À propos du rôle

En tant que Technicien.ne de Maintenance Utilities, vous serez responsable des interventions techniques et des améliorations dans le cadre de la maintenance des installations utilities du site de Braine, en suivant les règles établies dans le cadre de la GMAO. Vous travaillerez en horaire de jour, avec possibilité de rôle de garde.

Avec qui vous allez travailler

Vous collaborerez avec une équipe dynamique au sein du département Support Services. Ensemble, vous travaillerez en étroite collaboration avec les utilisateurs pour améliorer et développer les installations utilities. Vous interagirez également avec diverses parties prenantes pour assurer le bon fonctionnement et la maintenance des équipements.

Ce que vous allez faire

Vous participez aux améliorations et développements des installations Utilities.
Vous effectuez la maintenance préventive et curative des équipements.
Vous signalez toute anomalie, erreur ou incident à la hiérarchie.
Vous préparez et rédigez des instructions de maintenance et des dossiers techniques.
Vous assurez la documentation pré et post opérations de maintenance.
Vous suivez les règles GMP et GLP et maintenez les normes de sécurité et environnementales.

Intéressé/e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes

Minimum un A2 dans le domaine technique avec minimum 3 à 5 ans d’expérience dans la maintenance d’équipements ou un bachelier en électromécanique.
Expérience antérieure dans une société pharmaceutique ou agro-alimentaire souhaitée.
Connaissance approfondies des utilities (vapeur, eau, chauffage, ventilation) et techniques du froid, HVAC.
Capacité à lire et interpréter des dessins électriques, mécaniques, pneumatiques et hydrauliques.
Très bonne connaissance du français ; connaissance pratique de l'anglais technique est un plus.
Pragmatique, rigoureux et capable de travailler en autonomie.
Bon esprit d'équipe et compétences communicationnelles.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

埼玉：Packaging Staff（工程責任者候補） (Saitama, Saitama, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

【チームについて】

現場の安全と品質を最優先にし、継続的な改善を重視しています。チームは相互に学び合い、知識を共有しながら、工程改善や効率化に取り組みます。部門内外と連携し、円滑なコミュニケーションを通じて成果を最大化します。

【主な業務内容】

・安全な作業環境を維持し、労働災害を防止する

・包装工程の管理と安定稼働を推進する

・品質データを分析し改善施策を実行する

・生産計画と人員配置を最適化し納期を遵守する

・設備保全や導入計画を立案し実行する

・チームメンバーへの教育と指導を行う

【必須資格・経験・スキル】

・高校卒業以上
・医薬品GMP、化粧品GMP、食品安全マネジメントシステム（FSSC22000）、またはISO 9001に基づく品質マネジメントシステムの理解および運用経験

・生産、包装、工程管理の実務経験、または製造設備に関わるエンジニアリング／サービスエンジニアとしての実務経験

・品質マネジメントシステムや工程管理の仕組みに関する理解を有すること

・PCスキル（Excel、Word、Outlook等）

【あれば尚可の資格・経験・スキル】

・品質関連法規の理解と実務への応用力

・製造設備の導入、保全、立上げ、トラブルシューティング経験

・設備適格性評価（IQ/OQ）、バリデーション、試運転、性能確認等の経験

【求める人物像】

・関係者と円滑に連携できるコミュニケーション力

・向上心のある方（英語学習についても意欲的な方）

担当リクルーター：堀口

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBで働く魅力

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

Global Physical Asset Manager - Infrastructure & HSWB Assets (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Global Physical Asset Manager – Infrastructure & HSWB Assets who is analytical, collaborative, and strategic to join our Global Physical Asset Management / Transversal Asset Fleet Management team, based at our UCB campus located in Braine-l’Alleud, Belgium, or Bulle, Switzerland.

About the role

Who you will work with

What you will do

You will co-develop global asset management standards, governance principles, and lifecycle methodologies across infrastructure and HSWB (Health, Safety & Well-Being) assets.
You will lead modernization and renewal strategies using risk-based, data-driven asset insights and prioritization.
You will maintain a consolidated fleet view covering asset condition, compliance, supportability, performance, and investment needs.
You will manage lifecycle strategies for infrastructure, underground assets, and safety-related HSWB systems.
You will ensure asset decisions reflect prevention, protection, compliance, operational safety, and enterprise risk expectations.
You will partner with key functions to build business cases and align investments with enterprise objectives.

Interested? For this role, we are looking for the following education, experience, and skills:

You hold a Master’s degree in engineering, asset management, facilities, or a related technical field.
You bring strong experience in asset management, lifecycle management, and technical risk management.
You understand infrastructure, underground assets, safety systems, lifecycle needs, and degradation mechanisms.
You can build business cases linking asset decisions to resilience, cost competitiveness, COGS, and EBITDA.
You communicate complex technical topics clearly and influence senior stakeholders with practical recommendations.
You are fluent in French and have full professional proficiency in English; IAM certification is a plus.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Science Liaison, Neurology, Rockies region (Denver, Colorado, US)

Make your mark for patients

UCB is looking for a clinically experienced, science-driven, and patient-focused Medical Science Liaison (MSL) to work on the Epilepsy & Rare Syndromes team for the Rockies geography.

To ensure optimal coverage and engagement within the territory, candidates are ideally based in major hub cities in Las Vegas, NV, AZ, NM, UT, CO, and ID.

About the role

The Medical Science Liaison (MSL), Rockies will engage with key scientific and medical influencers to advance understanding of UCB’s Epilepsy and Rare Syndromes portfolio. This role fosters collaborative, science-driven partnerships with key stakeholders to support optimized patient care. The MSL will provide scientific exchange, contribute insights to medical strategies, and drive patient-focused initiatives within the local health ecosystem.

What You’ll Do:

Stay current with research and clinical data related to epilepsy and rare syndromes.

Execute targeted stakeholder engagement strategies to identify local needs and opportunities.
Provide meaningful medical insights to support medical strategies and initiatives.
Represent UCB at scientific conferences and educational events.
Collaborate cross-functionally to enhance patient care and contribute to medical projects as needed.

May lead/support other Medical Affairs projects or activities as assigned.

Who You’ll Work with:

Build and manage trusted, peer-level relationships with Key Opinion Leaders (KOLs), clinical investigators, and patient advocacy groups

Interested? For this role, we’re looking for the following education, experience, and skills

Minimum Requirements:

Doctorate (PhD, PharmD, MD, DPM, or DO) with a minimum of 3 years’ experience as an MSL

NP/PA with a minimum of 3 years’ experience as an MSL or minimum of 3 years of direct clinical experience in relevant therapeutic area or 5 years in the pharmaceutical industry.
Must reside within the assigned territory.

Valid driver’s license and ability to travel 60-80% in the designated territory.

Preferred Qualifications:

Clinical or professional experience in epilepsy and/or rare syndromes.
Strong scientific communication and presentation skills.
Ability to actively listen, identify opportunities, and deliver solutions.
Self-motivated, able to work independently and collaboratively within a cross-functional team.

This role requires 70-80% in-field engagement across the Rockies region

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Safety Specialist (Tokyo, Tokyo, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

※ご応募の際は英文と日本語文両方のCVが必要になります。

JOB SUMMARY

Primary Purpose / Regulatory Responsibilities:
• Responsible for ensuring Pharmacovigilance systems, operations and procedures are in place within the local organization for all territories assigned to the Affiliate as delegated
• Back up (or primary when delegated) contact for pharmacovigilance at the Affiliate
• Support the operational management of 1-2 medium or 1 highly complex Affiliate/country

MAJOR RESPONSIBILITIES

Support the Local Safety Officer to ensure oversight and management of Affiliate PV responsibilities as delegated/applicable:

Pharmacovigilance System

• Implement and maintain a pharmacovigilance system for the UCB products authorized in the territory and ensure compliance with applicable regulatory and company requirements;
• Identify and clearly articulate evolving local needs (regulation changes, eco-system changes, etc.) impacting Pharmacovigilance and as required work collaboratively with corporate Pharmacovigilance teams to develop and implement solutions; Provide input to harmonize global/local processes and to secure compliance; Work in close collaboration with corporate Pharmacovigilance teams to ensure that local obligations are managed and compliance to local authorities is maintained and secured;
• Maintain quality management system related to pharmacovigilance, including management of Standard Operating Procedures (SOPs), Associated Instructions (AIs) and documents (e.g. forms, templates) to describe local processes and requirements and perform regular gap analysis as needed in order to ensure alignment with global SOPs; Maintain oversight of local deliverables delegated to service providers;
• Ensure timely management of deviations and risk mitigation by defining appropriate CAPAs and ongoing trend analysis as appropriate.
• Maintain a functional connection with the Qualified Person for Pharmacovigilance (Global/EEA QPPV) e.g. participating in regular Local Safety Officer (LSO) meetings organized by corporate Pharmacovigilance;
• Ensure that the required local information for the Pharmacovigilance System Master File (PSMF) is made available to the EEA QPPV office, either directly or through local delegations (UCB colleagues or third parties);
• Ensures that adequate back-up processes are available

Proactive Regulatory Intelligence
• Maintain thorough knowledge of the local current pharmacovigilance regulatory requirements and landscape plus proactively monitor for emerging regulations and communicate such to corporate teams (including EEA QPPV), local stakeholders;
• Perform Impact assessment, gap analysis and implementation strategy for new or updated regulations and notify Global/EEA QPPV (as applicable), corporate Pharmacovigilance and relevant stakeholders.

Health Authority inspections and Audit readiness
• Ensure inspection and audit readiness of the relevant local departments in full collaboration with corporate Pharmacovigilance and Quality Assurance;
• Participate in and manage pharmacovigilance audits and inspections, perform root cause analysis, ensuring timely identification and implementation of respective Corrective Actions Preventive Actions (CAPAs);

Stakeholder Management
• Engage in transversal collaboration with affiliate and corporate stakeholders to secure pharmacovigilance compliance;
• Engage external stakeholders e.g. scientific community, patient advocacy groups, regulators and pharma industry for insights that leads to solutions for patients.

Other accountabilities for the role may include some or all the tasks, responsibilities such as –

• Support the LSO in operational management of 1-2 medium or 1 high complexity Affiliate/country.
• Collaborate as Deputy LSO for another country outside of direct Affiliate responsibility or another Affiliate as applicable
• Act as back-up SME for other Affiliates/countries
• Support effective, smooth management of Partnerships/vendors additionally for at least 1 countries/Affiliates

EDUCATION & QUALIFICATION

Bachelor's Degree

Other : HCP based education (such as physician, pharmacist, nurse) or any relevant graduation/experience in medical-scientific area (such as PhD/master in biological sciences or related degree)

COMPETENCIES

Specific skills

• Expert in pharmacovigilance, with an in-depth expert knowledge of associated regulatory requirements;
• Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives to meet compliance requirements;
• Have good interpersonal skills, ability to work independently in matrix organizations;
• Team working and networking promoter;
• Qualities of authenticity, resilience and adaptability;
• Communicates personal views clearly, even if they may be opposed by others;
• Be a Role model, with high level of integrity and honesty, both internally and externally. Ability to inspire peers, stakeholders and others;
• Excellent oral and written communication skills as the position requires to interact across multiple levels and with diverse functions (e.g. commercial, quality, regulatory, legal, medical) within and outside UCB (e.g. regulators, patients, HCP’s, Pharma industry associations);
• Excellent verbal and written communication in English and local language as required (specify any local language skills according to local requirements, if any);
• Good meeting preparation, facilitation skills
• Demonstrated ability to understand, analyze, and summarize scientific and medical information;
• Professional demeanor, team orientated, self-motivated, and ability to effectively engage with stakeholders;
• Problem solving:
a) Experience and ability to identify risks or issues, propose solutions or alternatives; Ability to identify gaps, perform trend analysis and implement risk mitigation strategy
b) The Ability to understand and use technology, knowing its limitations and understanding the risks and the precautions that usage requires

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBで働く魅力

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

Clinical Development Lead - Raleigh (Raleigh, North Carolina, US)

Make your mark for patients

We are looking for a Clinical Development Lead to join us in our Clinical Development team, based in any of our Brussels (Belgium), Monheim (Germany), Slough (UK) or Atlanta/Raleigh (US) offices.

About the role

As a Clinical Development Lead, you have the opportunity to leave a lasting impact on patients’ lives by driving innovative, patient-centric clinical strategies in a highly visible, high-stakes environment. Reporting to senior R&D leadership, you will lead the end-to-end design and execution of global development programs, working cross-functionally to translate science into access, and strategy into action.

Who you’ll work with

You’ll collaborate with global thought leaders, guide multifunctional teams, and influence decisions that shape both science and the business. You will report into the Global Head of Clinical Development for Immunology

What you’ll do

Set the global clinical development strategy for assigned asset(s), ensuring alignment with TPVP, regulatory requirements, and commercial goals.
Lead external engagement with global thought leaders, investigators, and stakeholders to continuously refine strategy based on emerging insights and unmet needs.
Design and adapt robust clinical development plans that integrate the latest scientific, regulatory, operational, and payer perspectives—balancing innovation with executional feasibility.
Oversee the execution of pivotal studies and regulatory submissions across all relevant markets, ensuring clinical excellence, data integrity, and timely delivery.
Shape clinical narratives and regulatory strategy, acting as a key representative in interactions with global health authorities and strategic partners.
Contribute to corporate strategy, supporting business development initiatives and representing the clinical perspective in asset evaluations.

Interested? For this position you’ll need the following education, experience and skills:

Basic Requirement:

Advanced degree (MD, PhD, PharmD, or equivalent).

Preferred Requirements:

Track record of leading complex global programs across multiple indications.
Familiarity with digital health technologies, real-world data, and AI-enabled trial innovation.
Ability to lead through ambiguity, make informed decisions in uncertainty, and drive results across organizational boundaries.
Strategic mindset with a bias for innovation, speed, and operational excellence.
Exceptional communication and stakeholder management skills, including C-suite level.
Global experience and cultural fluency; willingness to travel internationally as needed.

This positions reasonably anticipated base salary range is $236,800 - $310,800. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

#TeamUCB

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Analytical Compliance and Risk Program Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for an Analytical Compliance and Risk Program Lead who is strategic, collaborative, and quality-minded to join our team Analytical Industrialization Program / Industrialization & Network Planning, based at our UCB campus located in Braine-l’Alleud, Walloon Region, Belgium.

About the role
You will lead a global analytical compliance and risk program that helps UCB anticipate regulatory expectations and strengthen analytical control strategies across the product lifecycle. You are going to shape governance, support consistent risk-based approaches, and ensure stakeholders have access to the right standards, processes, and training. In this role, you will help protect compliance across methods, specifications, stability, impurities, and analytical regulatory topics for commercial products and future lifecycle management activities.

Who you will work with

You will partner with cross-functional leaders across analytical, regulatory, quality, industrialization, and lifecycle management activities to align expectations and accelerate decision-making. You will collaborate with subject matter experts, Corporate Process Owners, regulatory intelligence networks, and external industry groups to translate evolving expectations into practical standards. You will also represent UCB in expert forums and act as a trusted point of contact during audits, inspections, and regulatory discussions linked to analytical compliance.

What you will do

• Chair the Analytical Compliance & Risk core team and drive global alignment on priorities, decisions, and risk posture.
• Maintain analytical compliance governance across methods, specifications, stability, impurities, and related regulatory topics.
• Anticipate emerging risks through regulatory intelligence, benchmarking, and input from subject matter experts.
• Secure compliant, consistent responses to pharmacopeial changes, monographs, audits, inspections, and authority questions.
• Coach stakeholders and Corporate Process Owners on analytical compliance expectations, standards, and decision frameworks.
• Represent UCB in external expert groups and influence industry approaches to analytical compliance.

Interested?

For this role, we are looking for the following education, experience, and skills:

• You hold a Bachelor’s, Master’s, or Ph.D. in a relevant scientific discipline.
• You bring at least 10 years of experience in the pharmaceutical or biotech industry.
• You have strong experience in analytical CMC and regulatory guideline implementation.
• You understand analytical control strategies, including methods, specifications, stability, impurities, and specification setting.
• You have experience with risk management and compliance in a global regulatory environment.
• You have supported audits, inspections, or responses to FDA, EMA, PMDA, or other health authorities.

What you will bring

This is an opportunity to shape enterprise standards, influence external thinking, and provide visible leadership in a role with direct impact on analytical compliance, product quality, and regulatory confidence. For this role, we are looking for the following education, experience, and skills:

• You hold a Bachelor’s, Master’s, or Ph.D. in a relevant scientific discipline.
• You bring at least 10 years of experience in the pharmaceutical or biotech industry.
• You have strong experience in analytical CMC and regulatory guideline implementation.
• You understand analytical control strategies, including methods, specifications, stability, impurities and specification setting.
• You have experience with risk management and compliance in a global regulatory environment.
• You have supported audits, inspections, or responses to FDA, EMA, PMDA, or other health authorities.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Business Analytics Lead TW/HK/SEA (Taipei, Taipei, TW)

Make your mark for patients

You will work as a dedicated Business Analyst Lead in close collaboration with Patient Impact Teams to enable data-driven decisions. Your key responsibilities include:

• Market & Insights: Develop a deep understanding of the local market and therapeutic areas (e.g., Rheumatology, Dermatology, Epilepsy, Lennox-Gastaut, Myasthenia Gravis); generate actionable insights and deliver analytics solutions to address key business questions.

• Launch & Strategy: Drive and support launch readiness strategies and project follow-up for new products and indications in collaboration with local teams and regional stakeholders, including the Intercontinental Analytics community.

• Performance & Forecasting: Manage performance through robust insights generation and support accurate forecasting, ensuring reliable projections to guide both strategic and operational decisions.

• Collaboration & Innovation: Partner with local and regional stakeholders to implement strategic imperatives and foster innovative business thinking through holistic, end-to-end analytics.

COMPETENCIES:

• MSc in Biotechnology, Economics, Financials or Medical related university degree

• Significant experience in consultancy, pharmaceuticals, or healthcare sector (+5-10 years)

• Excellent understanding of the pharmaceutical G2M data landscape

• Strong analytical and problem-solving skills with good business acumen

• Team player with the ability to work independently

• Excellent communication and stakeholder management skills

• Fast learner, curious and comfortable with ambiguity

• Fluent in Local Language & English (if different)

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Downstream Biomanufacturing Process Expert (Bulle, Gruyere, CH)

Make your mark for patients

UCB is embarking on one of the most significant investments in its history through the development of a new state-of-the-art biologics manufacturing campus in Georgia, USA.

We are looking for talented, curious and ambitious individuals who want to make a lasting impact and contribute to shaping the future of biologics manufacturing at UCB.

We are looking for a Downstream Biomanufacturing Process Expert who is collaborative, proactive and innovative to join us in our Internal Manufacturing team, based at our UCB campus in Bulle, Switzerland.

About the role

Who you’ll work with

What you’ll do

Represent manufacturing in project discussions and ensure operational needs are reflected in facility design, systems and ways of working.
Translate technical, process and user requirements into clear project inputs that support practical and future-ready manufacturing solutions.
Review technical documents and data to support sound decisions for purification, filtration and buffer preparation processes.
Work with manufacturing sites and cross-functional partners to gather best practices, operational insight and lessons learned.
Promote strong health, safety, environmental and quality standards in daily project decisions and deliverables.
Stay informed on industry developments and help bring new technologies and modern manufacturing approaches into the project.

Interested? For this role we’re looking for the following education, experience and skills

Degree in a relevant scientific or engineering field, or equivalent experience in biopharmaceutical manufacturing.
Experience in biopharmaceutical operations and large-scale drug substance or purification projects within the pharmaceutical industry.
Strong knowledge of mammalian biopharmaceutical production, buffer preparation, process operations and supporting digital tools and systems.
Ability to communicate clearly, write technical documentation and collaborate effectively across functions and stakeholder groups.
Experience working in regulated manufacturing environments, including inspections, audits and compliance-focused decision-making.
Willingness to adapt to project variabilities and a rapidly evolving work environment
Fluent in English; French is an advantage.
Regular travel to Belgium and occasional travel to the United States may be required during conceptual design and basic design phases.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Science Liaison Rheumatology- Georgia & Alabama (Atlanta, Georgia, US)

Make your mark for patients

About the role

The Medical Science Liaison (MSL) is a professional who serves as a key field-based scientific partner to healthcare providers and decision-makers, medical professional associations, and internal UCB colleagues. This professional will be responsible for executing key medical strategies to enhance and positively impact patients living with chronic inflammatory diseases.

Who you will work with:

This position will support our Immunology Patient Value Unit (PVU) in an assigned geography of Georgia and Alabama.

What you’ll do:

Maintains deep scientific knowledge in areas of Rheumatology.
Delivers clinical value propositions and engages with key decision-maker stakeholders in medical groups, IDNs, and regional payers
Identifies and supports potential research expansion projects/collaborations, medical advisors, and educational partnership opportunities
Conducts local roundtables and education programs that aim enhance Key Opinion Leaders (KOL)s understanding of unmet clinical needs
Serve as a scientific expert at key medical and scientific conferences, advisory boards, clinical investigator meetings, and internal meetings.
Supports field-based cross-functional teams to provide medical expertise in access engagements as needed
Reviews and critiques scientific publications to help inform healthcare trends in Rheumatology
Collects, analyzes, and communicates information concerning therapeutic area, treatment options, emerging standards of care, and competitive intelligence
Addresses medical information inquiries
Provides effective clinical presentations to internal and external audiences and tailors presentations to meet specific audience needs through peer to peer scientific exchange
Assesses feasibility and serves as the primary liaison between UCB and investigator for unsolicited Investigator-Initiated Studies (IISs) from inception to publication
Provides field updates regarding topics of interest for creation and/or updating of Standard Response Letters

Interested? For this role we’re looking for the following

Minimum requirements

Doctorate degree (PharmD, MD, DO or PhD in a relevant field) required.
Valid US Driver’s License and with no more than 3 moving violations in the past 2 years
Must reside within the assigned territory
Must complete initial training and successfully pass all assessments within 90 days of hire

Extensive travel (up to 75%) is required, including overnights and some weekends.

Preferred Requirements

Rheumatology, Dermatology, Immunology, Infectious Disease, or Oncology experience strongly preferred.
2-3 years of field medical experience required
Prior product launch experience preferred.
Business acumen with a solid understanding of the pharmaceutical industry
Basic knowledge and understanding of health economic principles and clinical trials

*This position's reasonably anticipated base salary range is $134,000 - $204,000 annually. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Digital Technology Lead, Omnichannel Marketing (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Digital Technology Lead, Omnichannel Marketing to join our Global Digital Technology team based out of Atlanta, GA (hybrid, onsite 2 days/ week)

About the role

The DT Lead, Omnichannel Marketing is accountable for providing technical leadership, execution, and capability creation and standardization for US Omnichannel projects, specifically related to UCB digital marketing efforts (websites and email marketing). The role owns, from a technology and capability standpoint, all HCP, Patient, Corporate, and Medical websites (US) and will manage the full end-to-end scope (intake, delivery, support, strategy and innovation). The role will be supported by contract project management resources and is accountable for managing associated budgets, contracts, and scope across the project execution lifecycle.

Who you’ll work with

The role will partner closely with our Immunology, Neurology, and Rare Disease Business Units, Omnichannel, Corporate Communications, Medical and Analytics and Insights Teams as well as the larger global technology team to translate business needs into technical solutions and capabilities that can be implemented and leveraged across the US organization.

What you’ll do

Partner with the different US stakeholders which are developing patient solutions beyond the drug, and align with US leaders on the translation of their strategic commercial goals into roadmaps of digital capabilities.
Drive the Digital Business Transformation (DBT) roadmap of the ecosystem of patient & HCP platforms & solutions, embracing:
- front-end technologies (websites, mobile apps, social media),
- journey orchestration technologies (CRM capabilities & personalization of services)– patient/hcp data engineering & management technologies
- disruptive patient/hcp solutions like multi-sided patient platforms & A.I. applications
Act as thought leader to frame the integration of innovative & transformative digital initiatives (globally and/or locally developed) into the local US eco-system of solutions offered to the patient/hcp, ensuring a true added value for them and for the company.
Demonstrate a deep understanding of the current but also future eco-system of digital solutions which can be proposed to patients and hcps, aligning with the ambitions of the Commercial teams (G2M teams & Missions), but also on the best practices coming from Legal, Patient Safety, QA, Regulatory Affairs, …
Guide business stakeholders in technology choices, including for initiatives delivered in partnership mode. Bring an outside-in view on future technology trends, including the leveraging of global IT assets and ensure the team is up-to-date with digital capabilities of the future.
Challenge business ambitions to focus on realistic, achievable yet impactful solutions (Business Case approach)
Design, Develop, Deploy (Project Delivery) and Operate (Operational Excellence) the Web and omnichannel platforms & solutions offered by UCB towards US patients and hcps.
Deliver projects in close collaboration with all parties involved (business and IT, internal and external partners), following the IT project methodology.
Ensure patient/hcp solutions are TSSC (trustworthy, secure, safe and compliant). Work with the global IT teams to ensure such solutions are developed or integrated and operated.
Ensure compliance of the solutions to global process and legal requirements, follow validation guidelines and SOPs (respecting the UCB QMS, GxP & SaMD regulations).
Leading cross-functional project teams & fostering integration and shared ownership
Manage the team of IT resources delivering and maintaining the patient/hcp solutions in the US, as well as the budgets linked to all of them
Follow market trends and industry best practices with the aim of sharing the acquired knowledge inside UCB and of applying it to propose innovative solutions.
Actively take part in the implementation of the IT strategy, ensuring the appropriate leveraging of technology skills from other IT teams.

Interested? For this role we’re looking for the following education, experience and skills

Required:

Bachelors Degree
10+ years in IT with recent experience supporting pharmaceutical omnichannel digital marketing, digital strategy and execution

Preferred:

Strong experience with Digital Marketing, Website Design/Build, CRM/e-mail Marketing, personalization, data platforms, and digital engagement technologies
Knowledge of core digital marketing competencies applied in a patient engagement context
Experience managing cross-functional teams and external partners with diverse internal & external competencies
Strong understanding of data privacy (HIPAA/PHI/PII), consent laws, security, infrastructure concepts
Ability to evaluate emerging technologies through a business value and hcp/patient impact lens
Evaluation, design, development & deployment of digital patient/hcp solutions beyond the drug, including patient/hcp platforms & software as medical device (web technologies, content management systems, digital marketing practices, email/sms/social channels, etc)

This positions reasonably anticipated base salary range is $148,000 – $195,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Neurology Specialty Sales Representative, Columbus, OH (Columbus, Ohio, US)

Make your mark for patients

Make an impact where it matters most. Join UCB as a Neurology Specialty Sales Representative and become a trusted partner to physicians, clinics, and healthcare decision-makers—helping improve access, affordability, and support for people living with epilepsy and neurological rare diseases. In this high-visibility, field-based role in the Columbus, OH market, you’ll shape outcomes across the care continuum by building strategic relationships with integrated health systems, payers, pharmacies, and patient advocacy organizations.

This territory includes the geography of the greater Columbus area, extending to Huntington, WV, Parkersburg, WV, and Charleston, WV.

Candidates need to reside within the territory.

About the role
The Neurology Specialty Sales Representative executes marketing and sales strategy by mastering brand messaging, targeting, and digital tools to deliver persuasive, high-impact customer experiences tailored to distinct customer segments, while upholding the highest ethical standards. The role is accountable for delivering territory- and brand-level goals and key performance indicators through data-driven prioritization and smart resource allocation, ensuring marketing initiatives are implemented efficiently to achieve sales objectives and advance UCB’s patient value commitment.

What You’ll do
• Deliver territory performance by achieving/exceeding sales objectives while operating with the highest ethics, integrity, and promotional/operational compliance.
• Develop, execute, and refine a territory business plan aligned to strategy and KPIs (quarterly and weekly) by using data to prioritize accounts, set reach/frequency, and overcome barriers.
• Build deep disease-state and product expertise, including patient journeys, standards of care, treatment drivers, and—where applicable—the infusion process.
• Engage and support stakeholders across the care continuum (treating/referring HCPs, integrated health systems, hospitals/affiliations, pharmacies, sites of care, labs, payers, and patient advocacy organizations), including key thought leaders, by using UCB-approved resources and participating in relevant conventions/meetings and community disease-awareness efforts (as appropriate).
• Partner with payers and UCB payer/market access colleagues to keep providers current on coverage to help maximize patient access and affordability.
• Deploy resources to scale impact—marketing programs, omnichannel/digital engagement, speaker programs, and educational events (e.g., Lunch and Learns)—on time, within budget, and in compliance with UCB standards.
• Collaborate as part of the “One UCB” team by continuously improving through learning and feedback, and by completing required training/administration; overnight travel outside the territory may be required.

Who you’ll work with
• Internal (UCB): Marketing; payer access/market access; and cross-functional field colleagues (as part of the “One UCB” team) to align messaging, share insights, and coordinate stakeholder strategy.
• Healthcare providers: Treating and referring physicians, pharmacists, and other HCPs.
• Health systems & sites of care: Integrated health systems, hospitals/affiliations, and intermediate & long-term care facilities.
• Access stakeholders: Maintain strong relationships within the payer landscape to ensure providers are informed on coverage; collaborate with the payer access team to ensure all relevant stakeholders are working with the most up-to-date information to maximize access and affordability for patients using UCB products.
• Community partners: Patient advocacy organizations, plus pharmacies and labs as part of the broader care continuum.

Interested? For this position, you’ll need the following education, experience and skills:
Minimum Qualifications:
• Bachelor's degree.
• Minimum of 5 years of field-based experience in specialty healthcare and/or Neurology, calling on customers at a variety of call points (e.g., academic centers, community-based hospitals, and private practice offices), understanding of account-based selling, inclusive to Neurology or specialty market segment.
• Ability to travel overnight up to 60% within the territory to meet routinely with all targeted customers.
Preferred Qualifications:
• Promoting products specific to CNS/neuroscience, including epilepsy.
• 1 or more years of rare/orphan drug experience (to include epilepsy) or buy and bill; oncology, hematology, and/or Specialty Pharmacy knowledge.
• Proven, documented track record of delivering consistent sales results.
• Demonstrated ability to maximize the impact of multichannel/digital tools aligned to strategy and tactics within the scope of the territory's needs.
• Experience in biologic therapy administration within a healthcare network and/or community setting to designated site.

This position's reasonably anticipated salary range is $120,000-158,000 annually. The actual salary offered will consider internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien Équipements de Laboratoire (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Technicien·ne Équipements de Laboratoire

Nous recherchons un·e Technicien·ne Équipements de Laboratoire rigoureux·se, proactif·ve et orienté·e qualité pour rejoindre notre équipe Site Technical Support / Lab & Process Maintenance & Periodic Control, basée sur notre campus UCB situé à Braine-l’Alleud, Brabant wallon, Belgique.

À propos du rôle

Dans ce rôle, vous assurerez la performance, la fiabilité et la conformité des équipements analytiques utilisés dans nos laboratoires. Vous contribuerez directement à la continuité des activités en réalisant la maintenance, la qualification et les contrôles périodiques des équipements, tout en garantissant le respect des exigences GMP et des standards de sécurité.

Avec qui vous allez travailler

Vous rejoindrez l’équipe Lab Equipment Support et collaborerez étroitement avec les Project Leaders, les équipes Qualité, Validation et les laboratoires. Vous travaillerez également avec des fournisseurs externes dans un environnement dynamique où la coopération et l'amélioration continue sont essentielles.

Ce que vous allez faire

Vous allez réaliser la maintenance, la qualification et les contrôles périodiques des équipements analytiques.

Vous allez vérifier la conformité des interventions et assurer la fiabilité des équipements.

Vous serez responsable de la rédaction et de la revue de la documentation GMP.

Vous allez coordonner les interventions techniques avec les fournisseurs externes.

Vous allez suivre les écarts, retards et actions correctives associées.

Vous allez contribuer aux audits et aux initiatives d’amélioration continue.

Intéressé·e ?

Pour ce rôle, nous recherchons les qualifications, expériences et compétences suivantes :

Bachelier en chimie, biochimie, microbiologie ou domaine scientifique similaire.

Expérience en laboratoire analytique et en gestion d’équipements de laboratoire.

Bonne connaissance des exigences GMP et des systèmes qualité.

Maîtrise du français ; une compréhension de l’anglais est souhaitée.

Capacité à travailler de manière autonome tout en favorisant la collaboration.

Intérêt pour les outils informatiques ; SAP et Empower sont des atouts.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Associate Scientist (Cambridge, Massachusetts, US)

Make your mark for patients

We are seeking to hire a lab-based (non-hybrid) scientist to support early research at our Boston R&D Hub located in Cambridge MA. This scientist will have responsibility for executing assays for identification of small molecules therapeutics across UCB’s therapeutic areas of interest. They will also help to validate novel biological targets. Please note: For this particular role, we will not be able to sponsor the successful candidate for work authorization in the United States now or in the future, including taking over an existing work Visa.

Major Accountabilities/Responsibilities:

Work with team to develop, troubleshoot, and validate new assays
Generate cell models for screening and to mimic disease biology
Have accountability for achieving drug project milestones and delivering on objectives
Be involved in planning, optimizing, and executing on projects

Interested? For this position you’ll need the following education, experience and skills:

Minimum Required Qualifications:

BS degree with 4-6 years or MS degree with 2-4 years of applicable research experience with scientific track record
2+ years of experience with the design, development, optimization, and prosecution of cellular and biochemical assays for identification and evaluation of novel molecular entities
Direct hands-on experience with cell and molecular biology techniques and culturing human cell lines
Good communicator, with good presentation and organizational skills
Scientist who can work with some supervision but also to thrive in a multidisciplinary team environment

Preferred Experience & Skills:

Experience with small molecules/ligands/therapeutics is preferred
Working knowledge or experience with CRISPR screening approaches is a plus
Knowledge of targeted protein degradation is a plus
Neuroscience and/or immunology background is a plus

Salary:

This position’s reasonably anticipated base salary range is $86,400 to $113,400 per year. The actual salary offered will consider internal equity and may also vary depending on the candidate’s region, job-related knowledge, skills and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Data Foundations Analyst (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Senior Data Foundations Analyst who is collaborative, proactive, and solutions oriented to join our Commercial Data Operations team, based at our U.S. headquarters in Atlanta, Georgia. This hybrid role requires a minimum of 40% on-site presence and 5% domestic travel.

About the Role

You will serve as a key member of UCB’s Data Governance team, owning the intersection of data stewardship, financial operations, and vendor management. In this role, you will manage commercial data assets and contracts, oversee budget planning activities including operating expense forecasting, accruals management, spend tracking, and annual planning cycles, and ensure licensed data is used compliantly across the organization. You will act as the primary coordinator for vendor relationships, Statements of Work, purchase orders, and third-party data-sharing agreements while maintaining data catalogs, access controls, and governance processes. Success in this role requires strong financial acumen, process ownership, attention to detail, data governance knowledge, and the ability to manage vendor relationships, budgets, contracts, and competing priorities with a high degree of accuracy and accountability.

Who you’ll work with

Internally, you will partner with: Finance, Information Technology, Procurement, Legal, Data Governance, Commercial Data Operations, and business stakeholders across the organization to support budgeting, data access, compliance, and operational initiatives.

Externally, you will work with: data suppliers, software and data vendors, consulting partners, and authorized third parties to manage contracts, data licensing agreements, vendor performance, and data-sharing approvals.

What you’ll do

Manage Commercial Data Operations financial activities, including annual budgeting, forecasting, accruals, spend tracking, and operating expense management.
Own vendor management processes, including Statements of Work, purchase orders, contract routing, approvals, renewals, and supplier relationships.
Serve as the primary point of contact for third-party data-sharing agreements, ensuring compliance with licensing and usage requirements.
Administer data governance policies, access management controls, data catalogs, and metadata standards to support data quality and stewardship.
Partner with Finance, Information Technology, Procurement, Legal, and business stakeholders to support data acquisition, compliance, and operational initiatives.
Evaluate and manage relationships with data providers and vendors, identifying opportunities to maximize the value of data investments.
Lead recurring governance and information management meetings, communicate key updates, and support continuous process improvement efforts.
Analyze business needs, manage competing priorities, and implement solutions that improve operational efficiency, compliance, and data accessibility.

Interested? For this role we’re looking for the following education, experience and skills
Minimum Experience/Skills Required:

Bachelor’s degree in Data Science, Information Technology, Risk Management, Accounting/Finance, or comparable field
4+ minimum years of experience in finance, data governance or in a related role
Proficiency in web portal tools and MS Office tools, incl. Outlook, Excel, PowerPoint, Word, and Visio
Basic understanding of Data Systems, System Architecture, and Data Warehouses

Preferred Experience/Skills:

Ability to manage priorities, tight deadlines, and expectations on multiple tasks with a high degree of quality, while managing shifting business needs
Ability to routinely demonstrate strong quantitative, analytical, and complex problem-solving skills without supervision
High degree of leadership, integrity, and work ethic with a positive attitude
Strong learning agility and self-motivation, with a focus on patient value creation in a dynamic environment
Programming language experience (SQL, Python, R)

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Patient-Centered Outcomes Research (PCOR) Lead (Germany) (Monheim, Mettmann, DE)

Make your mark for patients

About the role

Who you will work with

What you will do

You will lead the development and implementation of patient experience evidence strategy on clinical outcome assessments (COAs) from early development through to full lifecycle management.
You will lead research activities supporting the selection, development, validation, interpretation, and implementation of PRO/COA measures.
You will provide subject matter expert input into strategic documents, tactical plans and target patient value profiles, as well as into clinical documents, eg, study protocols, analysis plans, clinical reports.
You will provide subject matter expert input into regulatory and HTA briefing packages and interactions..
You will lead scientific dissemination (eg, peer-reviewed publications, abstracts) in line with publication strategies.
You will build relationships and partner with external groups to advance methodological frameworks and acceptance of patient experience evidence to inform external healthcare decision making.
You will be an inspiring ambassador to contribute to organizational awareness on the value of patient experience evidence.

Interested? For this role, we are looking for the following education, experience, and skills:

Master's degree, PhD, MD, or equivalent qualification in a relevant scientific discipline.
Significant experience in biopharmaceutical, medical device, or academic environments within PRO/COA, or patient preference research.
Expertise in PRO/COA development, validation, and implementation in clinical research, including strong knowledge of qualitative and quantitative scientific methodologies and evidentiary requirements by regulatory and HTA bodies
Experience in clinical development, regulatory and HTA interactions.
Excellent stakeholder management, communication, influencing, and cross-functional collaboration skills in a matrix organization.
Proven project leadership capabilities with experience managing complex global initiatives

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Lead Immunology ECE (posting Poland) (Field Based, Field Based, PL)

Make your mark for patients

This role is based at our UCB offices in Warsaw, Poland or in Prague, Czech Republic.

About the role

Who you’ll work with

The Immunology MSLs and Medical Solution Leads in the ECE Cluster report directly to this role.

What you’ll do

Enable regional medical strategic direction aligned with global and European priorities.
Foster development for your team of Medical Science Liaisons and Medical Solution Leads.
Welcome and support medical talent across countries in the cluster.
Subject matter expert in immunology, ensuring strong therapeutic area acumen across the organization
Ensure high-quality field planning, execution, and activity follow-up.
Translate complex evidence and data into clear, patient-relevant insights for stakeholders.
Cultivate compliant collaboration with partners and external healthcare experts.

Interested? For this role we’re looking for the following education, experience and skills

Master or PhD in a scientific discipline; advanced medical or doctoral degree is valued.
Strong Medical Affairs, and leadership experience enabling teams’ growth, coaching, and supportive performance conversations.
Expertise in immunology or a closely related therapeutic area.
Strong understanding of clinical development, study management, and real‑world evidence.
Experience working in cross‑functional, regional, or matrix environments.
Digital literacy and comfort working in evolving medical ecosystems.
Successful experience in shaping strategic medical plans and following through from idea to patient impact.
Fluency in English, Polish and or Czech depending on your location, and travel readiness in the region are valued.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Key Account Manager, Tampa South (Tampa, Florida, US)

Make your mark for patients

We are looking for a Key Account Manager Sr. (KAM) in Rare Diseases who is patient-focused, exceeds sales objectives, and has worked in a complex selling environment to join us in our Rare Syndromes ∙ Epilepsy US team, based in the Tampa South territory. This geography will cover Tampa to Clearwater to Winterhaven to Naples. Candidates should reside in this territory.

About the role

Who you’ll work with?

What you’ll do

Exceed sales objectives by implementing marketing initiatives by developing and implementing business plans
Maximize impact by leveraging all available data sets and stakeholder input
Seek qualified leads and effectively profile new accounts, refine call planning/routing to optimize schedules
Working knowledge of the local managed care reimbursement
Emphasizes accountability and the highest standard of ethical conduct.

Interested? For this role, we’re looking for the following education, experience, and skills

Minimum qualifications

Bachelor's degree

Minimum of 8 years’ experience calling on customers at a variety of call points (e.g. academic centers, community-based, hospitals and private practice offices) both in person and virtual, inclusive of at least 5 years specialty, unless the market necessitates otherwise

Preferred Qualifications:

Master's degree, 2+ yrs rare/orphan drug experience

Promoting products specific to CNS/neuroscience, including epilepsy

Prior experience calling on Epileptologists and Neurologists in the territory

New product launch experience
Specialty pharmacy/REMS experience
Proven, documented track record of delivering consistent sales results

This positions reasonably anticipated base salary range is $144,000-$189,000 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Principal Scientist PK/PD (Slough, Berkshire, GB)

Make your mark for patients

We are looking for a Principal Scientist, Non-Clinical PKPD, who is innovative and agile to join us in our Clinical Development Sciences Group, based at the R&D site in Slough, UK, then Windlesham, Surrey (2027).

About the role

The Non-Clinical PKPD group sits within the Quantitative Clinical Pharmacology (QCP) function of Early Clinical Development & Translational Science (ECD-TS) Department. Our goal is to use integrated quantitative approaches as an essential strategic driver from target to market to bring differentiated solutions to patients. We are driving the quantitative integrated strategy of pharmacokinetics and pharmacology (e.g. PKPD, Systems modelling and clinical pharmacology/pharmacometrics) together with DMPK activities throughout the entirety of the lifetime of projects, from target identification through to life cycle management.

Who you’ll work with

We operate and collaborate closely with colleagues in Development Sciences, which, as a department, is responsible for providing strategy and support in bioanalysis, immunogenicity, safety, pathology, and regulatory activities. Work with external partners, academic institutions, CROs and consultants as required.

What you’ll do

Develop and drive the nonclinical PKPD strategy for projects. Communicating effectively ensuring implementation in projects.
Ensure translation from in vitro data and in vivo nonclinical studies to prediction of efficacy and safety in patients.
Initiate and engage in multifunctional collaborations to facilitate the advancement of drug candidates and build a thorough knowledge of drug pharmacology and PKPD, leading to quantitative translation to the clinic.
Build PKPD models of sufficient complexity to allow hypothesis testing and inform decision-making.
Represent the interests of QCP internally and externally in matters relevant to mechanistic PKPD and contribute to enhancing the scientific reputation of Non-Clinical PKPD, QCP and UCB.
Provide required support and input into regulatory study protocols, reports and summaries, and regulatory submission documents.

Interested? For this role you will need the following education, experience and skills

PhD in relevant discipline (pharmacology, pharmaceutical sciences, pharmacokinetics/pharmacodynamics, system biology or related fields).
Good understanding of pharmacology and pharmacologic processes related to disease and drug mechanisms.
Expertise and proven application of PKPD methods and concepts in support of drug discovery and development; systems modelling experience would be advantageous
Demonstrated experience in developing and executing effective non-clinical PKPD strategies from early discovery through to clinic.
Demonstrated experience and leadership skills working within a matrix environment with a wide range of internal stakeholders including Non-Clinical Safety, Bioanalysis, Clinical Pharmacology and Translational Medicine.
Experience in using modelling and simulation packages such as Phoenix, Berkeley Madonna, R and Monolix.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Principal Scientist - Colloidal & Granular Materials Characterization (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Principal Scientist – Colloidal & Granular Materials Characterization who is collaborative, curious and self-motivated to join us in our Development Sciences team, based in our Braine-L’Alleud campus, in Belgium.

About the role

You will play a key role in generating scientific insight that supports product development decisions. Working across a broad range of materials and therapeutic approaches, you will connect particle and materials properties to product manufacturability, performance and stability. You will design and interpret experiments, explore new analytical approaches, and communicate clear recommendations that help move development forward.

Who you’ll work with

You will be working in a team that combines deep materials science expertise with a practical, Quality by Design and collaborative mindset. You will partner with colleagues across formulation, analytical sciences, process development and device development, while also working with external research and technology partners. This is a team that values shared learning, innovation and high-quality science.

What you’ll do

Generate materials and particle insights across modalities (NBE, Gene Therapy and NCE) that support product design and development decisions.
Plan, run and interpret experiments using a broad range of characterisation techniques (including laser diffraction, dynamic imaging, DLS, rheology, mechanical behavior, …), adapting approaches to modality-specific needs:
- Protein aggregation, silicon droplets / subvisible particles.
- Colloidal systems (nano particle complex formation and isolation, …).
- Crystalline, amorphous materials.

Explore how material properties, formulation ingredients and process conditions affect product manufacturability (e.g., solid oral dosage forms, biologics processing, advanced delivery systems including viral/non-viral vectors) and performance.
Perform and interpret advanced chemical and spatial imaging (e.g., IR, SEM-EDX, Optical microscopy, XCT, …) on materials to understand microstructure.
Apply QbD principles, mechanistic understanding, and multivariate analysis to establish critical material attributes (CMAs).
Partner with colleagues and external collaborators to solve complex scientific challenges.
Share knowledge through reports, presentations and mentoring.

Interested? For this role we’re looking for the following education, experience and skills

Doctoral degree, or equivalent experience, in materials science, engineering, physical sciences or a related field.
Minimum 5 years of industry experience in pharmaceuticals or another relevant scientific field.
Hands-on experience in colloidal and granular materials characterisation.
Confidence working with complex scientific data and drawing practical conclusions.
Ability to work across teams and manage multiple priorities effectively.
Strong communication skills and a collaborative, reliable working style.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Procurement Category Lead - Market Insights & Patient Services (Anderlecht, Brussels, BE)

Make your mark for patients

What You’ll Do

Develop and execute global category strategies across research procurement, data acquisition, and medical and patient services procurement.
Lead and develop global category teams, ensuring alignment to common standards, governance, and strategic priorities.
Build and manage strategic relationships with research agencies, data providers, and patient services vendors.
Negotiate and oversee complex commercial agreements, including data licensing, research services, and patient support contracts.
Drive value creation through supplier optimization, commercial innovation, and improved return on research and data investments.
Partner with business stakeholders to align sourcing strategies with scientific, medical, and commercial priorities.
Ensure compliance with data privacy, healthcare regulations, and third‑party risk management requirements.
Shape procurement approaches related to digital, data, and AI‑enabled solutions while supporting responsible innovation.
Embed sustainability, supplier diversity, and ESG principles into procurement strategies and supplier selection processes.

Interested? For this role we’re looking for:

Bachelor’s degree required; Master’s degree preferred in business, life sciences, or a related field.
Significant procurement leadership experience across market research, data licensing, medical services, or patient services categories.
Strong experience leading global teams and influencing senior stakeholders within complex matrix organizations.
Knowledge of data privacy regulations, healthcare compliance frameworks, and third‑party risk management.
Strong commercial, negotiation, and supplier relationship management capabilities.
Digital and data fluency, with experience in analytics, AI governance, or data‑driven decision‑making.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

埼玉：Production Engineering Group Lead (Saitama, Saitama, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

製薬業界における生産技術・エンジニアリング領域のリーダーとして、埼玉工場で製剤・包装工程に関わる技術戦略の推進と組織マネジメントを担っていただきます。サイトリーダーシップチームの一員として事業戦略に直接関わりながら、設備導入・工程改善、新製品導入、技術移管、組織強化をリードし、ビジネス成果の創出に貢献いただく重要なポジションです。ローカルだけでなく、ベルギーをはじめとするグローバルチームとの協働機会も豊富にあります。

【チームについて】

Technical Services部門に所属し、生産技術グループを率いるポジションです。約4名のメンバーをマネジメントしながら、製剤・包装に関わる生産技術、設備導入、技術移管、バリデーション、工程改善など幅広い業務を統括します。サイトの将来を支える技術組織として、品質・生産性・安全性を高いレベルで実現するとともに、次世代リーダーの育成にも取り組んでいます。

【主な業務内容】

・PQ（性能適格性評価）以降のGMPに関するアクションのリードや技術的リーダーシップが主なミッションとなり、バリデーションマネージャーを兼任いただきます。

・サイト戦略およびTechnical Services部門の方針を生産技術グループの戦略・目標へ展開し、実行を推進する

・製剤および包装領域における技術サービス機能全体を統括する

・製造設備導入、新製品導入、技術移管プロジェクトのプロセスパートをリードする

・製剤・包装ラインに関するエンジニアリング活動を推進する

・設備の保守、校正、更新計画をサポートし、安定稼働を実現する

・GMPおよび関連法規制への適合を確保し、高品質な製造体制を維持する

・工程改善や設備改善による生産効率向上、コスト削減、安全性向上を推進する

・OPEX、CAPEX、人員計画の予算管理を行う

・包装資材開発を統括し、アートワーク開発をサポートする

・グローバルチームや外部サプライヤーとのパートナーシップを構築し、プロジェクトを推進する

・技術組織の変革および能力向上をリードする

・後継者育成やコーチングを通じて次世代リーダーの育成を推進する

・サイトリーダーシップチームの一員として戦略立案およびKPI達成に貢献する

・最新の製造技術やエンジニアリング知識を取り入れ、組織の競争力強化を推進する

【ポジションの魅力】

・サイト戦略に直接関与し、経営視点で意思決定に貢献できるポジション
・製造・包装領域の大規模プロジェクトをリードできる裁量の大きさ
・技術・人材育成の両面で組織成長を牽引できる役割
・ローカルおよびグローバル双方のステークホルダーと連携する機会
・設備・工程改善を通じてビジネス成果に直結するインパクトを実感
・次世代リーダー育成に関わり、自身のリーダーシップもさらに強化できる
・最先端の製造技術やエンジニアリング知識をアップデートできる環境

【応募資格】

・学士号以上

・製薬業界での技術開発またはエンジニア経験5年以上

・マネジメント経験3年以上

日本語ネイティブレベル、英語ビジネレベルの日英双方での高いコミュニケーション能力
製造工程および設備に関する専門知識

【求める人物像】

・成長志向とリーダーシップを発揮できる方

・ステークホルダーと連携を取って相互理解を図れる方

【応募方法】
・日本語の履歴書、職務経歴書と英語のCVを1つのファイルにまとめ、システムにアップロードしてください
・UCB社員からの紹介の場合は、応募時にその旨をシステム上でご記載ください。

担当リクルーター：堀口

（English follow）

Job Summary

Head of Production Engineering group leads and manages the group to provide technical services for the projects and engineering tasks, related to dosage form production and Packaging. She/he is responsible to realize Saitama site strategy as a member of site leadership team. She/he is also responsible to grow Saitama members.

Major Accountabilities/Responsibilities

• Translate the strategy, goals of Saitama site and Technical Service department into the group strategy and targets. Lead and manage the group to achieve the targets and realize the strategy.
• Control and manage the resource and capability to deliver the projects, related to the production engineering.
• Control and manage the OPEX, CAPEX and Head Count budget to meet the goal.
• Responsible to contribute for saving target.
• Lead and/or manage Dosage Form & Packaging projects.
• Responsible for the group to achieve following responsibilities.
- Mange and lead Dosage Form & Packaging projects and technical transfer of new products.
- Manage and lead the engineering work for Dosage Form & Packaging lines.
- Manage and lead the maintenance, calibration, and renewal work for Dosage Form & Packaging lines.
- Manage and lead repairment work for Dosage Form & Packaging lines.
- Manage and lead GxP and relevant raw execution for the Dosage Form & Packaging related matters.
- Manage and lead to Improve the Dosage Form & Packaging processes and equipment for a better efficiency and HSE.
- Manage and lead the packaging material development and design.
- Manage and lead artwork development.
• Grow next technical leaders and grow the group in leadership and technical skills.
• Responsible for the Saitama site strategy and KPIs comprehensively as a member of Saitama Leadership team.
• Build connection in UCB widely in both local and global for stakeholder management.
• Build good relationship with the suppliers in the market widely and manage and control them.
• Update the technical capability of the group according to the progress in technology.

Education & Qualifications

Bachelor's Degree

Technical development or Engineering experience for 5years in Pharma industry. And team management experience 3 years.

Competencies

Skill to build strategy and to breakdown the strategy into actions.
Professional skills to manage & lead people and teams.
Leadership to coach, motivate and energize people.
Have a strong Passion for achievements.
Have an established unique leadership (Authentic Leadership) style to lead the team to achieve goals.
Strong growth mindset to develop herself / himself and the team.
Strong communication skill in both Japanese and English which is enough efficient for stakeholder management.
Professional knowledge of GMP and relevant laws, especially for the process development and engineering area.
Have professional knowledge of production equipment, process, and basic knowledge of an analytical method transfer to execute Technical Transfer. And have a top-level knowledge in the industry for at least one of the areas of them.
Business level skill in statistics.
Professional knowledge in the packaging development area of pharma industry.
Basic knowledge in the artwork management of pharma industry

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBで働く魅力

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

QC Microbiology Technician (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Technicien·ne QC Microbiologie expérimenté·e, rigoureux·se et orienté·e solutions, pour rejoindre notre équipe QC Microbiologie, basée sur le campus UCB de Braine‑l’Alleud, Belgique.

À propos du rôle

Dans ce rôle, vous allez jouer un rôle clé dans la garantie de la qualité microbiologique des produits, du développement jusqu’au commercial. Vous allez réaliser des analyses microbiologiques de release, piloter les validations de méthodes et agir comme référent·e technique au laboratoire. Vous contribuerez activement à la routine du laboratoire ainsi qu’aux investigations, aux audits, à la digitalisation et à l’amélioration continue, dans le respect des exigences GMP.

Avec qui vous allez travailler

Vous allez évoluer au sein d’une équipe QC Microbiologie pluridisciplinaire, en collaboration étroite avec des technicien·ne·s, QC specialist , responsables de laboratoire et équipes de production. Vous travaillerez en partenariat avec l’équipe du QC microbiologie, la Qualité, et la Production dans un environnement collaboratif et orienté partage des connaissances.

Ce que vous allez faire

Vous allez réaliser des analyses microbiologiques pour le release, les IPC, les stabilités et investigations.

Vous allez conduire et documenter les validations de méthodes microbiologiques.

Vous allez être référent·e technique pour certaines méthodes analytiques et activités EM.

Vous allez soutenir les investigations, contaminations et prélèvements terrain.

Vous allez contribuer à la digitalisation des processus analytiques et documentaires.

Vous allez promouvoir les GMP, la sécurité, l’intégrité des données et l’amélioration continue.

Intéressé·e ? Pour ce rôle, nous recherchons le profil suivant :

Minimum 5 ans d’expérience dans l’industrie pharmaceutique.

Minimum 3 ans d’expérience en laboratoire de microbiologie ou EM.

Maîtrise des méthodes microbiologiques, EM, stérilité, endotoxines et biocharge.

Bonne connaissance des cGMP, pharmacopées, data integrity et principes ALCOA+.

Maîtrise du français et bon niveau d’anglais écrit.

Esprit proactif, orienté solutions et capable de gérer plusieurs priorités.

Flexible – travail occasionnel en week-end et jours fériés et participation à la rotation de l’horaire décalé 10h00-18h30 mis en place dans l’équipe de techniciens.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Media, Buffer & Logistics (MBL) Bio DS Operations Quality Manager (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

To strengthen our Bio DS Quality we are looking for a talented profile to fill the position of: Media, Buffer & Logistics (MBL) Bio DS Operations Quality Manager – Braine l’Alleud, Belgium.

About the role

The Media, Buffer & Logistics (MBL) Bio DS Operations Quality Manager will ensure the quality oversight of activities specifically related to media, buffer preparation, storage and local logistics within UCB’s new commercial biologicals drug substance facility at our Braine campus.

This role is crucial in ensuring compliance with regulatory and internal standards, ensuring a continuous presence of the MBL quality team on the floor, ensuring quality systems (Deviation, CAPA, CC) are followed and ensuring supply reliability. The MBL Bio DS Operations Quality Manager ensures that all these activities are performed in a solution-oriented mindset.

You will work with

You will work at the intersection of Quality and Operations, collaborating closely with Media, Buffer & Logistics teams, GMP Facilitators, Manufacturing and fellow Quality leaders. As a key partner to both operational and quality teams, you will help ensure compliant manufacturing processes, support issue resolution, oversee batch releases, and contribute to continuous improvement and inspection readiness across the site.

What you will do

Leadership and Management:

Build, lead and manage the MBL Quality Operations team, including hiring, training, and performance management.
Develop people capability & knowledge. e.g: by implementing training matrix and coaching for GMP Facilitators.

Ensure day-to-day quality oversight of the operations by GMP Facilitators.
Ensure a constant alignment with QA peers to provide a consistent quality support.

Perform continuous feedback within Quality Operations team and with Manufacturing counterparts.
Participate on the Bio DS Quality Operations Lead Team and act as deputy for Bio DS Quality Operations Head when needed.
Participate on regular alignment meeting with local and Global business partners (i.e., Manufacturing, MSAT, Quality Assurance Support, Quality Control, Regulatory)
Be part of/Challenge all MBL MSAT process improvement.
Propose solutions on major and critical issues encountered in MBL manufacturing.
Influence on way of working of other local department.

Quality Assurance

Responsible for the effective management of quality systems operating in MBL scope, including deviations (events), CAPA, batch review, change control, documentation, etc. Guarantee appropriately assessed from a quality perspective and are closed in time.
Responsible for the effective and right-first-time MB batch review process and MB intermediate batch release process.
Ensure all Process Orders (POs) related to MB manufacturing activities are released.

Organize thorough review / approval of GMP documentation and their appropriate application (e.g., gembas, spot checks, shopfloor).
Ensure quality representatives are involved in case of significant events occurring during MBL manufacturing activities.
Review and approve major or critical deviations, CAPA and Change Control.
Actively participate to the quality governance in place within the organization.
Support new product introductions in MBL production.

Regulatory Compliance

Performs internal inspections related to MBL activities.
Assist and / or explain topics related to MBL activities if requested during an internal or external inspection.
Ensure critical / major risks related to inspection readiness for MBL activities are appropriately escalated. Ensure relevant mitigations and documentation are available (e.g., power point presentation, preventive actions).
Participate in reviewing Annual Product Reviews.

Interested? For this position you’ll need the following education, experience and skills

Bachelor’s, master’s degree or an education in a relevant scientific discipline

Minimum of 5 years’ experience in the pharmaceutical industry

Fluent English & French communication (oral and written).

Proven experience in logistics within a regulated pharmaceutical environment
Prior people management experience is considered a strong asset
Experience with SAP and a strong understanding of its functionalities are essential
Ability to collaborate and influence across departments and levels
On-site presence required
Demonstrated experience in audit and inspection
Ability to face unstable environment and demonstrate agility to handle unpredicted changes
Ability to work effectively under pressure and adapt to changing priorities

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Principal Programmer, Atlanta, GA (Atlanta, Georgia, US)