Flexible Work, Better Balance
Monitor and control IPQA activities in sterile injectable manufacturing, filling, and packaging areas.
Ensure adherence to aseptic practices, gowning procedures, and cleanroom behavior.
Review and approve batch manufacturing records, line clearance, and critical process steps.
Conduct in-process checks, sampling, and verification of critical parameters during production.
Supervise environmental monitoring and ensure timely escalation of deviations.
Support investigations, CAPA implementation, and root cause analysis for quality issues.
Coordinate with production, QC, and engineering teams to ensure smooth operations.