<ul><li>To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing.</li><li>QA overview for clean room behavior and aseptic activity.</li><li>Review of batch processing records.</li><li>Review of all documents relating to the manufacturing, Packaging &amp; analysis report prior to batch release.</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 SOP’s, Specification, BPR issuance, Master Formulae and Records.</li><li>Preparation &amp; Review of process validation protocols and reports.</li></ul>

Trainee-IPQA