- Review QC raw data, BMRs, STPs, and specifications.
- Monitor compliance with cGMP, GLP, and documentation practices.
- Conduct GMP training sessions and maintain related records.
- Handle deviations, change control, CAPA, and non-conformance.
- Perform self-inspections, audits, and ensure ISO compliance.
- Familiarity with ISO 9001, 14001, and OHSAS standards
Required Skills
- Logical
- Team player
- Valuable in communication
- Knowledge of validation, qualification, and calibration processes.