· Conduct comprehensive market research on USFDA-approved / marketed drugs.
· Familiarity with core pharmaceutical and regulatory terminologies (e.g. NDA, ANDA, RLD, RS, Bioequivalence Study, API, DMF, ATC, etc.).
· Understanding of the drug discovery & development process, post-marketing information, and regulatory landscape.
· Positive knowledge of formulation science and basic chemistry concepts.
· Awareness of global regulatory authorities (preferably USFDA), including approval status of generics (approved / tentatively approved) and associated market pricing insights.
· Ability to systematically search, extract, interpret, and analyse data from various publicly available sources and prepare high-quality written drug/product profiles.
· Proficiency in MS Office, especially MS Excel.
· Strong analytical mindset with the ability to think critically and underlying assumptions.
· Excellent oral and written communication skills.