GMP QA Specialist - Deviation & Docs (1 Yr)

A recruiting firm is seeking a QA Specialist with GMP experience in Atlanta, GA, to provide quality support in a pharmaceutical manufacturing environment. This on-site role involves overseeing key quality assurance activities, including deviation management and documentation. The ideal candidate will have a relevant bachelor's degree and 1–3 years of experience in a regulated setting. Join to ensure compliance with industry regulations and support investigations across quality systems. #J-18808-Ljbffr