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MSAT Validation & Lifecycle Lead, Cell Therapy

Job in 2300, Leiden, South Holland, Netherlands
Listing for: Biopharma Careers
Full Time position
Listed on 2026-09-03
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist, Validation Engineer
Salary/Wage Range or Industry Benchmark: 110000 - 150000 EUR Yearly EUR 110000.00 150000.00 YEAR
Job Description & How to Apply Below
Bristol Myers Squibb Leiden Cell Therapy Facility seeks a Manager, MSAT Validation & LCM to lead validation activities, lifecycle management, and risk assessments for advanced cell therapy manufacturing. The role interfaces with process engineers and regulatory teams to ensure quality and compliance.
The ideal candidate has extensive biopharma validation experience, strong communication skills, and a track record of driving improvements in GMP environments.

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