Manager, MSAT Investigations

Bristol Myers Squibb; Leiden; On-site; EUR 120,000 - 180,000; Full time

Job summary

Bristol Myers Squibb Netherlands is seeking a Manager, MSAT Investigations to lead complex root-cause investigations in the Leiden Cell Therapy Manufacturing Facility. You will drive corrective actions, CAPAs, and risk assessments with cross-functional teams.

You will ensure audit readiness, support regulatory inspections, and mentor colleagues on Investigation Program fundamentals while staying current with industry standards.

Qualifications

• Experience in biopharmaceutical operations with a minimum of 5 years.
• Bachelor’s degree in science, engineering, biochemistry or related discipline.
• Proficient in quality systems and regulatory guidelines (cGMP).

Responsibilities

• Lead complex root cause investigations and CAPAs as a Senior Investigator.
• Collaborate with Process Engineering, Facilities, QA and QC for effective investigations.
• Proactively manage investigations to timely, compliant closure per KPIs.
• Present findings to site senior management and stakeholders.
• Apply Quality Risk Management and Operational Excellence to drive improvements.
• Support regulatory inspections and maintain audit readiness.
• Mentor colleagues on Investigation Program fundamentals.

Skills

Root cause analysis

Operational Excellence

Lean manufacturing

Cell therapy

cGMP compliance

Communication

Strategic thinking

Team leadership

Education

Bachelor's degree in science/engineering/biochemistry

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.

Bristol Myers Squibb Netherlands

Bristol Myers Squibb has been active in the Dutch market for over 50 years, employing people across a range of activities and business units in Utrecht, The Netherlands.

The Netherlands is also home to our first European Cell Therapy facility, located at the Leiden Bio Science Park, the largest life sciences cluster of The Netherlands. This new state of the art facility is focused on commercial manufacturing with capabilities for multi-product Cell Therapy manufacturing. You can become part of this exciting journey. Check out this video if you want to know more about it!

The Netherlands has everything it takes to become the medicines hub of Europe, the so-called Boston by the North Sea. As we continue to expand our footprint by building this new site, we are looking to grow our team.

Would you like to become an important chain in our worldwide network to bring this new personalized treatment to patients suffering from blood cancer? Join us and be a game changer!

For more information about Bristol Myers Squibb Netherlands, visit us at bms.com/nl or careers.bms.com/nl

Position Summary

The Manager, Investigations, Cell Therapy provides investigation leadership and support to the Leiden Cell Therapy Manufacturing Facility. The Manager will perform complex root cause analysis, work with stakeholders to identify corrective and preventative actions, facilitate impact assessments, ensure the Manufacturing Science & Technology team is audit ready, facilitate Annual Product Quality Reviews, and investigate product complaints.

Key Responsibilities

• Conducting and managing the resolution of complex/multi-functional root cause investigations, including impact assessments, CAPAs, and product complaints as a Lead Investigator
• Collaborating with many different groups/organizations as a Lead Investigator including Process Engineering and Support, Engineering and Facilities, Manufacturing Operations, Quality Assurance, and Quality Control
• Proactively managing the progression of investigations and CAPAs to timely and compliant closure per established KPIs
• Presentation of investigation findings to key stakeholders and site senior management
• Use of Quality Risk Management and Operational Excellence principles to facilitate risk-based decision-making, drive continuous improvement, and eliminate waste
• Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness; Actively supporting regulatory inspections
• Staying current with industry trends and BMS standards and participating in best practice forums consistent with function responsibilities.
• Coaching and mentoring of colleagues on Investigation Program fundamentals and best practice

Experience, Skills, and Abilities

• Experience utilizing root cause analysis tools and identifying corrective and preventative actions is required
• Experience with Operational Excellence and Lean Manufacturing is a plus
• Experience in cell therapy, biologics, or vaccine manufacturing/support desired
• Proficient in cGMP’s and multi-national biopharmaceutical/cell therapy regulations
• Excellent verbal/written communication skills and ability to influence at all levels
• Ability to think strategically, and to translate strategy into action
• Ability to prioritize and provide clear direction to team members in a highly dynamic environment
• Experience in product complaints and/or APQRs is a plus

Education and Knowledge

• Knowledge of science generally attained through studies resulting in a Bachelor’s degree in science, engineering, biochemistry or related discipline plus a minimum of 5 years’ experience in biopharmaceutical operations, or its equivalent is required

Working Conditions

• Position may require working in Clean-Room manufacturing environment approximately 15% of the time. Remainder of work is performed in an office environment.

#LI-Hybrid

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

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 workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin 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

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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. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1605647 : Manager, MSAT Investigations