- Review and ensure compliance of SOPs, BMRs, and protocols across sites
- Conduct internal audits and support external regulatory audits (USFDA, WHO, MHRA, etc.)
- Monitor CAPA implementation and change controls
- Ensure data integrity and GMP compliance across manufacturing units
- Evaluate product quality trends and prepare quality reports
- Coordinate with cross-functional teams for QA improvements
Skills:
GMP guidelines, documentation, audit handling, QMS, communication skills
Working Location ; Rabale
Qualification: B.Pharm / M.Pharm / M.Sc
Job Type: Full-time
Benefits:
- Paid sick time
- Paid time off
- Provident Fund
Education:
- Bachelor's (Preferred)
Experience:
- CQA: 2 years (Preferred)
Work Location: In person
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