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3.0 - 4.0 years
3 - 7 Lacs
gummidipoondi, thiruvallur
Work from Office
Position: Archival In-charge Vaccine Manufacturing Unit Department: Quality Assurance / Quality Systems Experience Required: 3 – 4 Years (GMP / Pharmaceutical / Biotech / Vaccine domain) Location: Manufacturing Site About the Role Experienced Archival In-charge to manage GxP documentation and record control in a regulatory compliant vaccine manufacturing environment. The role ensures readiness for WHO, FDA and national regulatory audits by maintaining integrity, traceability, and secure storage of critical records. Key Responsibilities Document & Record Control Receive, verify, classify, and archive batch records, QC data, validation documents, calibration/qualification records and supportin...
Posted 3 days ago
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