Onsite GMP Quality Lead — CAPA, Batch Release & Compliance
GSK
GSK US is seeking an on-site Quality Assurance professional at a United States manufacturing site to provide operational quality oversight. You will partner with production, laboratories, engineering and quality teams to ensure processes meet cGxP standards and regulatory requirements, reviewing batch records and approvals, and escalating quality risks. You'll coach staff on quality best practices, support deviations and CAPA, and help maintain inspection readiness while fostering a culture of #J-18808-Ljbffr GSK
Vacancy posted 1 day ago
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