Responsibilities
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
Positive in communication
Knowledge of validation, qualification, and calibration processes.