Cadila Pharma

• Literature search by Sci-Finder and evaluation, summary of literature search and finalization of ROS base on cheaper and commercially available raw materials. • Check and define the feasibility of proposed ROS, design the experiments and optimization of process • Handle CIP-project to ensure shortest process, best recovery and minimum RMC. • Responsible to resolve any issues/queries related to other departments such as QA, RA, Analytical, PE and Plant w.r.t. product process, scale-up, technology transfer, risk assessment, investigation of any failure, etc. • Evaluation of GTI and N-nitroso impurities in drug substance. • To develop cost effective process meeting regulatory quality and minimum environmental hazardous process by following cGMP & GLP guidelines. • Provide support to the subordinates to achieve the goal by using technical knowledge and experience. • Characterization of working standards of KSM, intermediates and finished products and impurity standard by using PXRD, 1H NMR, 13C NMR, IR, Mass, DSC, TGA and ICP-MS techniques. • Create novel ideas and implement them to create IP assets after discussion with IPR team and superior. (Patent filling) • Preparation of technical package for customers and process development report (PDR) and reviewed the documents. • Training and development of the team members. • Lab maintenance and ensure that all equipment used in the lab are calibrated, validated, clean and in good condition.

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