<ul><li>Assist in reviewing batch records, SOPs, and quality documentation for injection products.</li><li>Support in-process checks and validation activities under supervision.</li><li>Learn and follow GMP, WHO, USFDA, and other regulatory guidelines applicable to sterile manufacturing.</li><li>Participate in audits, deviation reporting, and investigation processes.</li><li>Help maintain documentation, filing, and traceability of quality records.</li><li>Coordinate with production, QC, and other departments for smooth operations.</li><li>Support training initiatives and continuous improvement projects.</li></ul>

QA Trainee Officer (Injection)