GMP QA Specialist – Deviation & Documentation Expert

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