3 - 8 years
4 - 9 Lacs
Posted:19 hours ago|
Platform:
Work from Office
Full Time
The QA Validation Sterile professional will be responsible for overseeing and ensuring the validation and qualification of sterile manufacturing processes, equipment, utilities, facilities, and computerized systems in compliance with cGMP, regulatory guidelines, and company standards. The role ensures that all validation activities support the consistent production of high-quality, sterile pharmaceutical products.
Acme Formulation
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