Ensure batch compliance with GMP documentation standards. Review batch production records (BPRs), perform process validation activities, handle deviations and CAPAs, manage SOPs, and support internal and external regulatory audits.
Requirements:
- B.Sc / M.Sc in Chemistry (Organic, Analytical, or General)
- Freshers with robust understanding of pharmaceutical QA principles are welcome
- Knowledge of cGMP documentation, deviation handling, CAPA, and change control
- Good communication and documentation skills
Work Location: Plot Nos. 292–296, Kadechur Industrial Area, Kadechur Village, Yadagir Taluka & Dist, Karnataka – 585221, India. Candidates must be willing to work from this location.