Validation Lead – CSV

Title: Validation Lead – CSV
Location: Wilmington, DE (Onsite/Hybrid)

independent visa

Client Looking For:

• Strong Computer System Validation (CSV) experience in Life Sciences / Pharma R&D.
• Must have knowledge of GxP, FDA 21 CFR Part 11, and GAMP 5.
• Experience leading validation activities, documentation, testing, and regulatory compliance.