cGMP Quality Documentation Specialist

A leading quality documentation firm in Virginia is seeking a Quality Documentation Coordinator to manage important quality documents in a regulated environment. Responsibilities include organizing and tracking records, supporting audits, and ensuring compliance with safety and cGMP standards. Ideal candidates should have a High School Diploma or GED, along with 1-3 years of relevant experience and knowledge of FDA documentation. This role offers a competitive pay rate and a supportive work environment. #J-18808-Ljbffr