Manager QA, EU Qualified Person Cell Therapy

Bristol-Myers Squibb Co; Leiden; Remote; EUR 110,000 - 150,000; Full time

Job summary

Bristol Myers Squibb is seeking a Manager QA, EU QP Cell Therapy for Europe and Rest of World Markets. The role focuses on implementing the Quality Assurance function and ensuring product quality for ATMPs in the EU and beyond.

You will act as Qualified Person for investigational and commercial cell therapy products, ensuring compliance with EU GMP/GDP and engaging with cross-functional teams to drive timely batch disposition and regulatory adherence.

Qualifications

• MSc (or equivalent) in a technical or scientific discipline and eligible to act as Qualified Person.
• EU Qualified Person eligibility as described in EU regulations.
• Extensive quality assurance/control experience in biotechnology (≈6+ years).
• Experience with aseptic manufacturing and cell therapy products.
• Excellent communication, collaboration, and dispute-resolution skills in a team setting.
• Strong organizational, project management, and problem-solving abilities.
• Thorough knowledge of GMP/GDP requirements and global regulations.

Responsibilities

• Act as Qualified Person under BMS Netherlands Operations BV licenses and perform duties per conduct code.
• Fulfil QP duties per EU regulations and ATMP guidelines.
• Interpret international, regional, and local regulations and ensure GMP/GDP compliance across EU/EEA and RO World Markets.
• Verify QP certification of ATMPs and IMPs for import into the UK per MHRA guidelines.
• Develop knowledge of cell therapy processes and commercialization plans.
• Collaborate with QA, Supply Chain, and site/vendor oversight functions to ensure compliant batch disposition.
• Support inspections and implement corrective actions where needed.
• Maintain and improve quality risk assessments and release processes.

Skills

Quality assurance

Excellent communication

Organizational skills

Problem solving

Attention to detail

Regulatory knowledge

Team collaboration

Computer proficiency

Education

MSc or equivalent in science/tech

EU Qualified Person eligibility

Job description

At Bristol Myers Squibb, our employees often ask, 'Who are you working for?' - a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Position Summary

The Manager EU QP supports in the implementation and execution of the Quality Assurance function and Quality Management System of BMS Netherlands Operations BV which will ensure product quality and compliance with all regulatory and corporate requirements for Investigational and Commercial ATMP (Gene Therapy) Products within Europe and Rest of World Markets as applicable. This position acts in its primary role as Qualified person for investigational and commercial Cell Therapy products within EU/EEA and Rest of World Markets as applicable. These duties and responsibilities are executed in accordance with the requirements of the BMS Netherlands Operations BV license and the Professional Code of Conduct.

Duties/Responsibilities

• Act as Qualified Person as per requirements of BMS Netherlands Operations BV licences and execute functions in accordance with Professional Code of Conduct
• Fulfil Qualified Person duties as defined in article 51 of 2001/83/EC, Annex 16, Annex 13 and the ATMP guidelines of Volume 4 of the EU GMP guidelines
• Interpret international, regional, and local regulations and apply those regulations within the GMP/GDP environment and the batch disposition process in the EU/EEA and Rest of World Markets as applicable.
• Perform the verification of QP certification of imported Advanced Therapy Medicinal Products (ATMPs) Investigational Medicinal products (IMP) into the United Kingdom in accordance with MHRA guidelines "Importing Investigational Medicinal Products (IMP) from countries on a list to Great Britain", as assigned
• Build up a deep knowledge of the cell therapy-based processes, technology and the specific treatments which are intended to be commercialized
• Interact with global, site, and vendor oversight Quality and Supply Chain functions to ensure a compliant, efficient, and timely batch disposition for cell therapies
• Participate in GMP- or GDP-related health authority inspections at Celgene Distribution BV, BMS Netherlands Operations BV and other BMS entities as required, respond to any noted observations, and ensure implementation of corrective actions
• Manage quality and compliance risks by conducting risk assessments and ensuring risk mitigation actions are taken
• Develop and maintain a release process which takes into account the specifics of autologous cell therapy treatments with staged release, treatment of OOS results and related risk assessments
• Conduct final review and approval of non-routine quality investigations related to batch deviations, batch disposition, and other quality systems for assigned products as required
• Identify and recommend product and process quality improvements
• Support BMS Netherlands Operations BV for implementing and maintaining and continuously improving the quality management system
• Author and/or revise procedures, work instructions, and Standards, as required
• Maintain compliance with personal training requirements
• Draft or review, negotiate with contractors, and recommend approval for Quality Agreements
• Participate in GMP audits of suppliers, and service providers as required

The Manager QA, EU QP Cell Therapy reports administratively and functionally to the Director, Disposition Operations – Cell Therapy.

Qualifications

• MSc (or equivalent) in a technical or scientific discipline and meets educational requirements for EU Qualified Person as described in Article 49 2001/83/EC and any national requirements
• Eligible to act as Qualified Person within EC/EEA
• Experience as Qualified Person preferred
• Extensive quality assurance/control experience in the biotechnology industry (equivalent to a minimum of 6 years experience), including audit, batch record review, change control, complaint handling and investigations experience
• Must have experience and good knowledge of aseptic manufacturing, biological products and/or cell therapy products
• Must have excellent communication skills, including excellent written, interpersonal, collaboration, negotiation and dispute resolution skills, with a team oriented approach
• Must have excellent organizational, project management and problem solving skills
• Must have thorough knowledge of pharmaceutical manufacturing, packaging, testing, and distribution processes and associated global regulatory GMP/GDP requirements (EU particularly), including a good knowledge of Advanced Therapy Medicines Product guidelines of the EU GMP Vol. 4 regulations
• Must have demonstrated understanding of the processes and interactions essential for ensuring and maintaining regulatory compliance
• Must have computer proficiency
• Must have superior attention to detail

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume,

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] with the Job Title and Requisition number.

Equal Employment Opportunity

Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.