Lead QA operations for pellets manufacturing ensuring cGMP compliance and audit readiness.
Key Responsibilities
- Ensure cGMP compliance and QMS implementation
- Handle deviations, CAPA, change control
- Review BMR/BPR and ensure process compliance
- Support audits
- Oversee validation and documentation
- Lead QA team and cross-functional coordination
Requirements
- M.Pharm/B.Pharm/MSc
- 10–15 years pharma experience
- Mandatory pellets manufacturing experience
- Exposure to regulated markets preferred