GMP Documentation Specialist II
Cosettepharma
Cosettepharma is seeking a candidate for a role involving the issuance of cGMP documentation to support daily processes. Responsibilities include managing documentation and ensuring adherence to Good Documentation Practices. The ideal candidate will have a High School Diploma, 5+ years in document control, and strong knowledge of cGMP and FDA requirements. Skills in Microsoft Office are essential. This position requires an organized individual able to work under pressure. #J-18808-Ljbffr Cosettepharma
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