Key Responsibilities:
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.