QA Documentation Specialist

A pharmaceutical company in Bedford, Ohio is seeking a Document Associate to manage document control for the manufacturing site. Responsibilities include creating and filing GMP documentation, authoring SOPs, and liaising with various functional groups. The ideal candidate should have an associate degree and relevant experience in pharmaceutical documentation and quality assurance. Compensation ranges from $22.60 to $38.00 hourly, based on experience and location. #J-18808-Ljbffr