Validation Manager- Injectable Venus Remedies (VRL)

8.0 - 13.0 years

6 - 15 Lacs

baddi

Work from Office

Role & responsibilities Strategic & Leadership: Lead the QA Validation function for sterile injectables manufacturing facility. Develop, implement, and periodically review the Validation Master Plan (VMP) . Provide strategic direction for validation activities in line with corporate and regulatory requirements. Mentor, train, and supervise the validation team. Validation & Qualification: Oversee qualification of facility, cleanrooms, HVAC, water systems, equipment, utilities, and computerized systems . Manage process validation, cleaning validation, aseptic process validation (media fills), and hold-time studies for injectables. Ensure timely revalidation and continuous verification activiti...

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