MSAT Validation & Lifecycle Lead, Cell Therapy
Job in
2300, Leiden, South Holland, Netherlands
Listed on 2026-09-03
Listing for:
Biopharma Careers
Full Time
position Listed on 2026-09-03
Job specializations:
-
Pharmaceutical
Regulatory Compliance Specialist, Validation Engineer
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.
#J-18808-LjbffrNote that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
Search for further Jobs Here:
×