Senior MES Validation Lead: CSV & GxP Compliance
RAIS USA
RAIS USA is seeking an experienced Senior CSV Consultant to support validation and compliance activities for MES and GMP-regulated systems within the pharmaceutical and life sciences environment. The consultant will work onsite at Concord, NC, and partner with Quality, Manufacturing, IT, and Compliance to ensure systems remain compliant with FDA 21 CFR Part 11, GAMP5, data integrity standards, and the system lifecycle. #J-18808-Ljbffr RAIS USA
Vacancy posted 1 day ago
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