Senior CQV Validation Engineer - GMP Facility Lead
Virtue America
Virtue America in California seeks a Senior Validation CQV Engineer with 9+ years in pharma/biotech to lead validation activities for a facility expansion and upgrade project. You will develop and execute CQV documentation, manage IQ/OQ/PQ, and ensure all systems remain in a validated state in a GMP environment. The role requires hands-on qualification of HVAC, water systems, HPLC, bioreactors, and analytical equipment, with strong data integrity and QMS experience. #J-18808-Ljbffr Virtue America
Vacancy posted 1 day ago
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