Job Location: Vadodara (Full Time)

Requirement: MSC (Life Sciences) / B.Pharma with 0-4 years of experience.

Candidate's profile: The candidate should possess sound knowledge of pharma drug approval process or drug chemistry or drug manufacturing. Softer skills like analytical and report writing will be valued. Experience in regulatory affairs will be preferred.

Job Profile: Tracking all Para IV litigation (patent litigation) updates from a public source and update it on to our proprietary database. Study the litigation along with drug complexities and determine the likely timeframe of first generic launch along with possible competition. The candidate will be required to be proficient in using various regulatory portals like USFDA

The job will require to create understanding of another drug database and publish weekly and monthly reports.