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• Prime responsibility is looking for overall manufacturing, component preparation , filling area of pre filled syringe & vial washing ,vial filling area. • Responsible for batch manufacturing & filtration activities. • Qualified visual inspector for in process tub inspection during filling. • Maintaining cGMP & good Aseptic Technique in aseptic area. • Actively Participated in smoke study & Media fill. • Attended trouble shooting in process equipment. • Involved in Scaleup batches, Development batches and PV batches activity for all stages like Formulation,Filling activity’s. • Monitoring of Issue, receipt and review of Batch manufacturing records as per cGMP. • Successfully faced the USFDA audit as a member of the production team.
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