Must have a Masters Degree in Pharmaceutical Sciences, Industrial Pharmacy or closely related field. Must have one 1 year experience in the field of quality assurance in the generic pharmaceutical industry. The experience must include inprocess quality assurance checks, sampling of incoming materials, inprocess samples, and finished products, recording of sampling and batch release in SAP ERP system, and maintaining inventory for DEA submissions. Must have strong knowledge in CGMPs; health safety; environmental protection; stability studies as per ICH guidelines; and change controls and deviations. Demonstrable skills in oral and written communications, independent judgement, problem solving and effective managing and adhering to timelines is required

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