MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable
Are you passionate about quality and keen to build your career in the pharmaceutical industry? We are hiring enthusiastic and dedicated individuals for our Quality Control (QC) Department.
Execute Analytical method Validation activities of drug substances API by using HPLC,GC and Spectroscopic techniques as per regulatory guidelines. Execution and coordination for Analytical method transfer activities of drug substances.
M.Pharmacy / M.Sc. / BPharm; Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols.
To search on various country patent databases to retrieve equivalent patent information, legal status etc., in different geographies. To prepare patent landscapes, analyze the patent content to summarize their claims and specification.
Regulatory Submissions Prepare, submit, and manage regulatory filings for API products, including new drug applications, amendments, and variations, while ensuring compliance with relevant guidelines and regulations. API Equipment Handling.
Monitor Cleaning of Reactor, Centrifuge, ANFD, Filtration System, Dryer, Miller, Sifter and Micronizer as per approved cleaning Records, SOPs. Execution of batch operations like material charging, extractions, workups, filtration, additions, centrifuging, drying, sampling and labelling.