QA Documentation & Compliance Specialist
Pharmavite
Pharmavite is seeking a Quality Documentation Specialist in Ohio to ensure quality across manufacturing processes. You will issue, track, review, and evaluate documents and records tied to GMP operations, supporting consistency and compliance. Responsibilities include reviewing batch records, non-conformances, and change controls; filing protocols; and coordinating with operations to resolve documentation errors. A strong attention to detail and English proficiency are essential. #J-18808-Ljbffr Pharmavite
Vacancy posted 2 days ago
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