I am a dedicated and detail-oriented M.Pharmacy graduate with a strong foundation in pharmaceutical sciences, drug regulations, quality assurance, and research.
I have hands-on exposure to analytical techniques such as RP-HPLC, UV spectroscopy, and chromatographic methods, along with practical knowledge of GMP, GLP, SOP preparation, documentation, ICH guidelines, CTD dossier basics, and validation concepts.
I am comfortable with scientific documentation, literature review, report writing, and basic data analysis, and I bring strong problem-solving, communication, time management, and teamwork skills.
My academic background includes a Master of Pharmacy and a Bachelor of Pharmacy, and I completed a project on analytical method development and validation for simultaneous estimation of Naltrexone and Oxycodone using RP-HPLC.
I also completed an industrial internship at Natco Pharma Ltd., where I gained exposure to pharmaceutical manufacturing processes, quality control procedures, laboratory practices, and GMP environments.
I am seeking an entry-level opportunity in regulatory affairs within medical devices or life sciences, where I can contribute my technical background while continuing to grow professionally.
I gained exposure to pharmaceutical manufacturing processes, quality control procedures, laboratory practices, and GMP.
This internship helped me understand industry workflows and strengthened my practical knowledge of pharmaceutical operations.
M.Pharmacy, Pharmacy
B.Pharmacy, Pharmacy
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