GMP & ISO 13485 Documentation Specialist

Katalyst Healthcares & Life Sciences is looking for a Documentation Management role in Ridgefield, NJ. The candidate will manage the lifecycle of production documents, ensuring compliance with cGMP regulations and ISO 13485 standards. Key responsibilities include reviewing Batch Production Records, collaborating with cross-functional teams, and utilizing software tools like SAP for documentation management. Strong organizational and communication skills are essential, along with 3-5 years of experience in a GMP manufacturing environment.
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