Lead Process Engineering Manager, Cell Therapy

Biopharma Careers

Leiden

On-site

EUR 90,000 - 140,000

Full time

3 days ago
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Job summary

Bristol Myers Squibb Netherlands is seeking a Manager, Process Engineering to lead the technical side of CAR-T therapy production at the Leiden facility, ensuring continuous, compliant, and efficient 24/7 operations. This role collaborates with Process Validation, MES/Automation, Manufacturing, and Quality to drive rapid, flawless delivery of high-quality products.

The ideal candidate has 8+ years in cGMP biologics manufacturing, strong process engineering and Lean manufacturing knowledge, and a

Qualifications

  • Deep knowledge of facility/clean room design, cell therapy processes, equipment and automation.
  • Hands-on experience with single-use technologies, closed systems, and cold chain/cryogenic technologies.
  • Experience working with external parties and/or leading cross-functional teams.

Responsibilities

  • Drive end-to-end process optimization and issue resolution on the production line.
  • Lead investigations and CAPA activities for OOS, deviations and process changes.
  • Ensure timely technical documentation reviews and approvals (SOPs, batch records, protocols).
  • Provide on-site and on-call support for operations and shopfloor topics.
  • Coordinate with MSAT, Manufacturing, Quality, and Supply Chain to ensure compliant, cost-effective delivery of therapies.
  • Lead changes and continuous improvement initiatives across the multiproduct facility.

Skills

Cell therapy
Process engineering
cGMP knowledge
Automation
Leadership
Cross-functional collaboration
Analytical troubleshooting

Education

Bachelor’s degree in science or engineering
Advanced degree preferred

Tools

Lean Manufacturing

Job description

Bristol Myers Squibb Netherlands is seeking a Manager, Process Engineering to lead the technical side of CAR-T therapy production at the Leiden facility, ensuring continuous, compliant, and efficient 24/7 operations. This role collaborates with Process Validation, MES/Automation, Manufacturing, and Quality to drive rapid, flawless delivery of high-quality products.

The ideal candidate has 8+ years in cGMP biologics manufacturing, strong process engineering and Lean manufacturing knowledge, and a

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