GMP QA Specialist - Deviation & Documentation Expert
The Voluntary Protection Programs Participants' Association, Inc
A pharmaceutical organization is seeking a QA Specialist with GMP experience for a one-year contract role located in Smyrna, GA. The candidate will provide fundamental quality assurance support, focusing on deviation management and GMP documentation in a regulated pharmaceutical environment. Responsibilities include quality assurance support, deviation investigations, compliance with GMP regulations, and collaboration with manufacturing and regulatory teams. Ideal candidates should have a Bachelor's degree in a life sciences field and 1-3+ years of relevant experience. #J-18808-Ljbffr The Voluntary Protection Programs Participants' Association, Inc
Vacancy posted 5 days ago
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