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 current 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

📌 Deputy General Manager/assistant General Manager - Quality Control - Formulations (10-20 Yrs) Bangalore (qa/qc & Regulatory Affairs)
🏢 Magna Global HR Services
📍 Bengaluru