Oversee sterile / injectable manufacturing operations
Ensure compliance with cGMP, WHO, USFDA norms
Handle aseptic processing, sterile filling, lyophilization
Review BMR/BPR and maintain documentation
Manage cleanroom operations and audit readiness
Required Candidate profile
Coordinate with QA, QC, Engineering teams
Handle deviations, CAPA, and investigations
Strong knowledge of aseptic practices & regulatory audits
Positive team handling skills