GMP QA Specialist: Deviation & Documentation Expert

A leading recruiting firm is seeking a QA Specialist with GMP experience to provide quality support in a regulated pharmaceutical environment. You will support quality assurance activities, focusing on deviation management and GMP documentation. The ideal candidate will have 1-3 years in the pharmaceutical industry, experience with deviation investigations, and a degree in a relevant field. This is an on-site, one-year contract role located in Smyrna, GA. #J-18808-Ljbffr