<ul><li>Assist in daily QA activities under supervision, ensuring compliance with cGMP and company quality standards.</li><li>Support review of batch manufacturing records (BMR/BPR) and related documentation.</li><li>Participate in in-process checks during manufacturing and packaging operations.</li><li>Help in preparation, revision, and control of SOPs and other QA documents.</li><li>Assist in deviation, change control, and CAPA documentation.</li><li>Perform line clearance activities before and after production or packaging operations.</li><li>Support internal audits and help maintain audit readiness documentation.</li><li>Ensure proper documentation practices and data integrity across departments.</li><li>Participate in validation and qualification activities when required.</li></ul>

QA Trainee Officer