GMP Manufacturing Deviation & Documentation Specialist

A biotechnology company located in Watertown, Massachusetts, seeks a Manufacturing Support Associate to provide hands-on support for GMP manufacturing operations. The role involves leading deviation investigations, conducting batch record reviews, and ensuring compliance with high-quality standards within a CDMO environment. The ideal candidate will have 3–5 years of experience in GMP manufacturing, strong documentation skills, and knowledge of GMP regulations. This is a contract position focused on the manufacturing function. #J-18808-Ljbffr