CQV Document Controller | GMP/GxP & Veeva Expert
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Verista in West Chester, Ohio, seeks an experienced Document Controller to manage controlled documents within a regulated pharmaceutical manufacturing environment. You will support Quality, Engineering, Validation, and Manufacturing teams, ensuring GDP-compliant documentation and meticulous record-keeping. Candidates should have hands-on Veeva Vault QualityDocs experience, strong attention to detail, and excellent communication skills to coordinate cross-functional reviews and audits. #J-18808-Ljbffr Socket.dev
Vacancy posted 2 days ago
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