The candidate should have experience in Parenterals and Freeze drying in Injectables.To Plan Man power as per production schedule on daily basis.To supervise filling and packing activities in compliance with cGMP guidelines and documentation.To optimize packing material consumption Vs yield, from batch to batch.To upkeep GMP environment.To possess through knowledge of Machinery and trouble shooting of themTo Prepare Master Batch Mfg. RecordTo Prepare and implement SOPs.Responsible for Effective implementation of QA systems as per cGMP, USFDA, WHO-GMP, MCA-UK, MCC-SA.Regulatory exposure is required.Rush cv's toMr.SaikishoreEmail :
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esired ProfileB.Pharm with 5 - 8 yrs experience


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