GMP Documentation Specialist: Records & Compliance Lead

A leading pharmaceutical company is looking for a Documentation Specialist to ensure the accuracy and compliance of production documents. The ideal candidate will manage the lifecycle of documentation, collaborate with multiple departments, and maintain compliance with cGMP and ISO 13485 standards. Applicants should have 3-5 years experience in a GMP manufacturing environment, strong organizational skills, and proficiency in Microsoft Office.

Full-time position located in Ridgefield, New Jersey.
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