GMP Document Control Specialist – Cell Therapy

A global biotechnology company is seeking a Document Control Specialist to support the document management process in a cell therapy manufacturing facility. The candidate will manage compliance within the Document Management System and ensure regulatory standards are met. Required qualifications include a bachelor's degree and at least 2 years of relevant experience. This full-time position in Raritan, NJ offers competitive compensation and benefits including medical, retirement plans, and generous paid time off. #J-18808-Ljbffr