QA Documentation Specialist — Pharma cGMP Compliance

A pharmaceutical company in Manassas is seeking a QA Associate for documentation compliance with cGMP standards. This on-site position entails performing inspections, managing document control systems, and overseeing quality assurance processes. The ideal candidate has at least two years of experience in a quality assurance role within pharmaceutical manufacturing and holds a college degree in a relevant science field. Strong documentation skills and an understanding of FDA regulations are essential for success in this role. #J-18808-Ljbffr