Regulatory & QA Documentation Specialist

A leading pharmaceutical company in West Warwick is seeking a Documentation Coordinator to maintain and control GMP documentation according to FDA regulations. The role requires managing the document lifecycle, supporting inspections, and ensuring compliance with quality standards. Candidates should have a degree in Quality or Life Sciences, along with 2–5 years of experience in an FDA-regulated environment. Strong attention to detail and knowledge of data integrity principles are essential for success in this position. #J-18808-Ljbffr