QA Documentation Specialist: Regulatory Compliance
US-Pharmalab-Inc
US-Pharmalab-Inc in North Brunswick, NJ is seeking a Specialist, Documentation to manage writing, distribution, storage and ongoing maintenance of our GMP documentation. The role ensures SOP compliance and alignment with 21 CFR Part 111 and 117, reporting to the Quality Assurance Manager with a dotted line to the Head of Quality Assurance. Responsibilities include creating and updating documentation, coordinating with internal teams to capture process details, and ensuring staff use current #J-18808-Ljbffr US-Pharmalab-Inc
Vacancy posted 1 day ago
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