GMP C&Q Documentation Lead — Owner’s Rep, Pharma
i-Pharm GxP
i-Pharm GxP seeks an experienced C&Q Documentation SME to support a major pharmaceutical project through C&Q and into operational readiness. The role will lead the review and approval of GMP documentation on behalf of the Owner, coordinating with Quality, Engineering, Vendors and Contractors to ensure timely, high-quality deliverables. The position focuses on GMP/C&Q documentation for isolators, downflow booths, fume hoods and related utilities, with on-site presence required one week per month. #J-18808-Ljbffr i-Pharm GxP
Vacancy posted 2 days ago
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