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    Liton Roy

    Experienced Pharmaceutical Professional

    Liton Roy is a renowned science and technology leader with a proven track record of over ten years in the pharmaceutical industry, specializing in various aspects from development to commercialization.

    His expertise spans across scientific and technical leadership, cloud technology development, single-use technology for sterile drugs and biologics manufacturing, and solid oral dosage, semi-solid, and sterile drugs development.

    With a Ph.D. from the University of Vermont and an M.S. from the Indian Institute of Technology, Kanpur, Liton has a strong educational background to support his extensive experience.

    He has served in key roles at prestigious organizations including Pfizer as a Principal Scientist, Teva Pharmaceuticals as the Manager of Analytical Research and Development, Mylan as Manager of Laboratory Operation, and Perrigo Company plc as an Associate Scientist.

    Liton Roy's skill set includes proficiency in ANDA, IND, NDA, CBE-30, PAS, and 505(b)(2) CMC support, along with an in-depth understanding of GLP, cGMP, USP, ICH, and FDA guidelines, showcasing his comprehensive knowledge and regulatory capabilities.

    He excels in managing multiple priorities, strategic analytical development, global CMC, process validation, technology development, and product lifecycle management, demonstrating his ability to thrive in cross-functional and global roles.

    Liton Roy
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    Location

    United States