- Ensure pharmaceutical products comply with GMP guidelines, company SOPs, and applicable regulatory requirements.
- Review and approve batch manufacturing records (BMR), batch packaging records (BPR), and other quality documents.
- Monitor in-process activities, deviations, CAPA, change control, and documentation compliance.
- Coordinate with QC, Production, and other departments to maintain product quality and compliance.
- Support internal audits, regulatory inspections, validation activities, and continuous quality improvement.
Preferred candidate profile
- M.Pharm / B.Pharm / M.Sc. in Chemistry or a relevant pharmaceutical discipline.
- 46 years of experience in Quality Assurance in the pharmaceutical industry.
- Knowledge of GMP, GLP, GDP, SOPs, BMR/BPR, deviations, CAPA, and change control.
- Experience in audits, regulatory compliance, and pharmaceutical documentation.
- Robust analytical, communication, and problem-solving skills.