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Quality Assurance Specialist managing document control, training administration, and product lot disposition in an eQMS to ensure cGMP/GDP compliance for pharmaceutical packaging and distribution operations.
Ensures compliance with QA/regulatory standards in biopharma manufacturing, reviewing documentation, auditing logs, and supporting investigations for GMP operations.
Supervises QA team ensuring cGMP compliance in drug/device manufacturing, oversees daily operations, and collaborates with cross-functional teams to maintain quality standards and resolve issues.
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