- Lead end-to-end Quality Assurance operations for Oral Solid Dosage (OSD) manufacturing.
- Ensure compliance with USFDA EU GMP MHRA WHO-GMP PIC/S and cGMP requirements.
- Lead and manage regulatory inspections customer audits and corporate quality reviews.
- Strengthen Quality Management Systems (QMS) including CAPA Change Control Deviations Risk Management Investigations APR/PQR and Validation oversight.
- Drive a solid culture of quality compliance operational excellence and continuous improvement.
- Collaborate with Manufacturing Quality Control Regulatory Affairs Engineering Supply Chain and Technical Services to achieve business objectives.
- Mentor develop and lead high-performing QA teams while building future leadership capability.