Bristol Myers Squibb Co is seeking a Manager, CSV Cell Therapy to lead qualification and validation activities for manufacturing and laboratory equipment at multi-use sites. You will own lifecycle deliverables, drive CFR 21 Part 11 compliance, and supervise vendors while developing validation plans and training staff.
The role requires a BS degree (or equivalent) and 5+ years in FDA-regulated environments, with strong collaboration across manufacturing, QA, and IT teams.
#J-18808-LjbffrCell Therapy CSV Lead: Validation & Compliance in summit at Unknown Company
This position is listed as full time and onsite.