GMP Documentation & Quality Specialist

Amgen Inc. in Ohio is seeking an experienced documentation professional to support GMP manufacturing. You will develop, review, and update SOPs, WIs, and protocols, manage deviations, CAPA and change controls, and provide clerical support for document control. You’ll liaise with cross-functional teams to implement changes and drive training documentation and continuous improvement. The role emphasizes accurate record keeping, timely processing, and maintaining current GMP standards in a #J-18808-Ljbffr