<ul><li>To perform IPQA activities at shop floor in each and every stage of manufacturing and packing.</li><li>QA overview for clean room behaviour and personnel hygiene .</li><li>Review of batch processing records.</li><li>Review of all documents relating to the manufacturing, Packaging analysis report prior to batch release.</li><li>Knowledge of APQR and CPV process.</li><li>Review of documents of respective areas and logbooks for adequacy and completeness.</li><li>QA overview for receipt of material from warehouse to production.</li><li>IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities.</li><li>Review and Control of SOPs, Specification, BPR issuance, Master Formulae and Records.</li><li>Preparation Review of process validation protocols and reports.</li><li>Executing the validation/revalidation activity in the absence of authorized person.</li><li>Any job activity assigned by HOD</li></ul>