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