Our client, has been a pioneer in the manufacturing of nutritional healthcare products in India and has emerged as a multi-product, multi-divisional pharmaceutical company that develops therapeutic formulations and distributes them worldwide.Responsible for overall in-charge of all quality control aspects of raw materials, in-process, finished products & documentation related quality system, which will cover :A facility audit of QC, QA, Production, warehouse, and engineering for cGMP complianceB Audit of Analytical validation documentsC Implementation of cGMP in the factory.D Monitoring of Third-party product statusE Co-ordination with Export Department for registration documents. Other Areas:- You will be responsible for monitoring adherence to various cGMP/GLP activities and laid down procedures in receipt, storage, testing, processing and dispatch of products.- You will coordinate the technology transfer for the new products and with Production for planning of analysis.- Reporting of monthly activities of the dept. and respective contract manufacturing management.What they are looking for:- M.Sc with 10+ years (B.Sc with 12+ years) overall experience in QC for formulations and with 4+ years of experience working in Plant QC/QA and experience in undergoing regulatory inspections. (ref:biojoby.com)
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