<ul><li>Having knowledge on Preparation, review, and control of SOPs.</li><li>Having knowledge of Controlling all master documents and maintaining distribution, archival and retrieval of documents.</li><li>Having thorough knowledge on QMS ( Handing of Change controls, Deviations, OOS, CAPA and market complaint ) documents, ensure compliance and CGMP is followed.</li><li>Having exposure of Preparation of process validation Protocol and report.</li><li>Having exposure for Review of documents like BMR, BPR, MOA and specification.</li><li>Should have good experience of regulatory audits like USFDA, EU, MHRA etc.</li><li>Should have good written and Oral communication skills.</li></ul>

Officer / Executive - Quality Assurance