The candidate must be capable of analyzing raw materials, finished products, and stability samples. Knowledge of AMV and QAMS will be given preference.
M.Sc Chemistry, B.Pharm, M.Pharm ; Preparation of IPQA SOPs, IPQA Checks, AQL, Line Clearance, Review of BPR, Audit & Compliance, Sampling of API & Drug Product, Document & Data Control, Control Sample Management.
Creating new opportunities for growing the business, organically and inorganically through in licensing of products for company's entry into international markets excluding US and India.
Strong understanding of pharmaceutical formulations and patent law basics. Proficiency in patent databases and search strategies.
Analytical mindset with excellent attention to detail. Good communication and technical writing skills.
M.Sc. / B. Pharm / M. Pharm. Review of Electronic data on various QC instrument Like HPLC, GC, FTIR, UV-Visible Spectrophotometer, TOC analyzer etc. Details experience on Audit Trail review of All QC instruments. Hands on Experience on Various QC instrument calibration like HPLC, GC, FTIR, Polarimeter, UV-Visible Spectrophotometer, Dissolution etc. Experience on Handling of OOS, OOT, OOC, Laboratory Incident investigation, Deviation etc.
Preparation of IPQA SOPs, IPQA Checks, AQL, Line Clearance, Review of BPR, Audit and Compliance, Sampling of API & Drug Product, Document and Data Control, Control Sample Management.