? Qualifications: Gujarat State FDA Approved Technical Person in Production Certification is mandatory
- M.Sc. / B.Sc. in Chemistry
- B.Pharm / B.Tech Chemical Engineering
- Minimum 4–5 years of experience in API/Bulk Drugs/ Pharmaceutical Manufacturing Industry
? Salary: As per industry norms
? Key Responsibilities:
✔ Review and endorse Batch Manufacturing Records (BMR) & Batch Packing Records (BPR)
✔ Ensure compliance with Valuable Manufacturing Practices (GMP)
✔ Verify raw materials, in-process materials & finished goods as per specifications
✔ Coordinate with QC for testing and product approvals
✔ Monitor critical process parameters and validated processes
✔ Execute validation protocols and reports (IQ, OQ, PQ)
✔ Handle process validation,
cleaning validation & equipment qualification
✔ Maintain Validation Master Plan (VMP) and revalidation schedules
✔ Develop and review SOPs related to validation activities
✔ Investigate deviations, perform root cause analysis & implement CAPA
✔ Ensure documentation compliance and data integrity