<ul><li>Ensure all activities comply with cGMP, regulatory, and company quality standards.</li><li>Review and approve batch manufacturing records (BMR/BPR) and ensure timely batch release.</li><li>Handle documentation control including SOPs, validation protocols, and change controls.</li><li>Monitor in-process quality checks and ensure adherence to quality procedures.</li><li>Participate in deviation, OOS (Out of Specification), and CAPA investigations.</li><li>Conduct internal audits and coordinate for external and regulatory audits.</li><li>Review qualification and validation documents for equipment and processes.</li><li>Ensure proper implementation of QMS elements like deviations, complaints, and recalls.</li></ul>

QA Executive