Bhavesh Barot
Principal Scientist -drug Product Development @Bristol Myers Squibb
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WORK HISTORY
Principal Scientist -drug Product Development @Bristol Myers Squibb
New Brunswick, NJ, US
Product Development Lead for oral solid and parenteral dosage form for novel pipeline assets• Lead and manage the development of pharmaceutical products, from conception to launch, in collaboration with cross-functional teams.• Conduct thorough research and analysis to identify potential drug candidates and develop effective product development strategies.• Design and execute experiments to evaluate the safety, efficacy, and stability of oral products, ensuring compliance with regulatory guidelines.• Oversee the formulation and process development of oral products, ensuring optimization of drug delivery and manufacturing processes.• Collaborate with external partners, such as contract manufacturing organizations, to ensure successful scale-up and commercialization of oral products.
EDUCATION
K. B. Institute of Pharmaceutical Education & Research
Doctor of Philosophy - PhD, Pharmaceutics
L.M. College Of Pharmacy
M. Pharm., Pharmaceutics and Pharmaceutical Technology
WIPO-UNIGE Summer School on Intellectual Property
DL 101 General Course on Intellectual Property Rights
L.M. College Of Pharmacy
B. Pharm.
ABOUT BHAVESH BAROT
Accomplished pharmaceutical scientist and formulation development leader with a Ph.D. in Pharmaceutical Sciences and 10+ years of experience advancing complex drug products from early development through commercialization. Recognized for building high‑performing teams, shaping CMC strategy, and delivering robust, scalable formulations across oral solid and parenteral modalities—including lipid nanoparticle–based systems- Expert in API characterization, formulation design, and end‑to‑end drug product development with a strong foundation in both scientific rigor and operational execution- Proven leadership in diagnosing and resolving development and manufacturing challenges through innovative technologies, data‑driven decision‑making, and deep process understanding- Strong command of QbD frameworks, including DoE, statistical modeling, and risk management, to enable efficient scale‑up, tech transfer, and commercial readiness- Extensive experience supporting global regulatory submissions (IND → NDA) with clear, concise, and scientifically sound CMC documentation- Effective cross‑functional leader, partnering seamlessly with Regulatory, Quality, Analytical, Operations, and Program Management to align strategy and accelerate timelines- Strategic thinker with a strong business mindset—skilled at evaluating risk, optimizing resources, and guiding teams through ambiguity and complex decision landscapes- Published 20+ peer‑reviewed papers and invited guest faculty at the University of Southern California, demonstrating commitment to scientific excellence and mentorship.
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