Role & responsibilities 1. Ensure compliance with GMP, cGMP, ISO, FSSAI and other regulatory requirements. 2. Prepare, review and maintain SOPs and quality-related documents. 3. Review BMR (Batch Manufacturing Records) and BPR (Batch Packaging Records). 4. Perform line clearance and in-process quality checks. 5. Handle deviations, CAPA and change control. 6. Conduct internal audits and support external/customer audits. 7. Investigate quality-related complaints and identify root causes. 8. Review and approve validation protocols and reports. 9. Maintain proper documentation and document control. 10. Coordinate with Production, QC, R&D; and Regulatory Affairs departments. 11. Ensure GMP implementation throughout manufacturing operations. 12. Monitor and improve the Quality Management System (QMS). Preferred candidate profile Preferred Male Candidates Required Qualifications
- B.
Sc / M.
Sc Chemistry
- B.
Pharm / M.
Pharm
- Biotechnology or Microbiology background