On-Site QA Documentation Specialist - Pharma (GMP/FDA)
Piper Companies
Piper Companies in Ridgefield, NJ is seeking an experienced Quality Assurance Technical Writer to join a growing pharmaceutical manufacturer. The role focuses on authoring and revising QA documentation and Master Batch Records to support sterile injectable production. Responsibilities include reviewing alterations to master batch records, advising manufacturing personnel on documentation standards, and ensuring compliance with FDA and GMP regulations using MS Office tools. #J-18808-Ljbffr Piper Companies
Vacancy posted 2 days ago
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