Rusan is a research driven pharmaceutical company having its Manufacturing Units in India and Worldwide Marketing of Pharmaceutical Formulation, Active Pharmaceutical Ingredients and Intermediates.
Monitor and verify the quality of raw materials, in-process materials, and finished products through regular inspections and testing. Investigate and resolve quality issues, deviations, and complaints related to manufacturing processes and products.
M.Sc. / B.Pharma. Operating equipment reactors, Sparkler Filter, Candle Filters, Centrifuge, Dryers as per SOP. Knowledge of GMP, cGMP, Data Integrity in USFDA and MHRA regulatory API manufacturing plants. Lupin pharma
To ensure cGMP compliance at the shop floor for Drug Substance (DS) manufacturing through effective line clearance, documentation review, in-process oversight, and quality systems activities.
QA professional experienced in GMP documentation review, process and cleaning validation, QMS management (Change Control, Deviation/Event, CAPA), analytical data review, SOP management, and regulatory compliance activities.