GMP Compliance Documentation Specialist

A pharmaceutical company is seeking a qualified candidate for a position involving the review of manufacturing documentation. The role includes ensuring compliance with cGMP, conducting batch record reviews, and maintaining documentation standards. Ideal candidates will possess strong MS Office skills, attention to detail, and the ability to work independently in a fast-paced environment. An Associate's degree or relevant experience in manufacturing quality documentation is required. Flexible work hours and the ability to lift 30 pounds are also necessary. #J-18808-Ljbffr