Responsible for overall Quality Assurance and Quality Control operations in the pharmaceutical manufacturing unit and ensuring compliance with GMP, WHO-GMP, and company quality standards.
Key Responsibilities
- Manage QA and QC activities.
- Ensure GMP and regulatory compliance.
- Approve SOPs, BMR/BPR, specifications, and quality documents.
- Handle deviations, CAPA, OOS, audits, and inspections.
- Monitor in-process quality and batch release.
- Ensure training and implementation of quality systems.
- Drive continuous quality improvement initiatives.