Dr. Prashant Devrukhakar

Dr. Prashant Devrukhakar

Project Trainee

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  • Timeline

  • About me

    Sr Manager at Eli Lilly | PhD at VIT, Vellore | M.S. (Pharm) at NIPER, Hyderabad | Ex-Novartis | Ex-USP

  • Education

    • L. M. College Of Pharmacy, Ahmedabad Gujarat University

      2004 - 2008
      B. pharm Pharmacy
    • VIT_Vellore Institute of Technology

      2014 - 2020
      Doctor of Philosophy - PhD Pharmaceutical analysis

      Title of my Ph.D. thesis is “Isolation and characterization of degradation products obtained from forced degradation study of active pharmaceutical ingredient.”

    • National Institute of Pharmaceutical Education and Research

      2008 - 2010
      M.S. (Pharm.) Pharmaceutical Analysis
    • Symbiosis Institute of Management Studies

      2011 - 2013
      Master of Business Administration (M.B.A.) Operations A
  • Experience

    • US Pharmacopeia

      Jul 2009 - Jun 2010
      Project Trainee

      I have successfully accomplish dissertation work titled as ‘Validated Stability Indicating RP-HPLC Assay Method for Combination of Antiviral Drugs’ under the guidance of Dr. K.V. Surendranath, Vice President, USP India Pvt. Ltd., Hyderabad and Dr. Nalini Shastri, Associate Professor, NIPER Hyderabad

    • United States Pharmacopeia India Pvt.Ltd

      Apr 2011 - Feb 2016
      Scientist II

      The United States Pharmacopeia (USP) is the official pharmacopeia of the United States, published dually with the National Formulary as the USP-NF. The United States Pharmacopeial Convention (usually also called the USP) is the nonprofit organization that owns the trademark and copyright to the USP-NF and publishes it every year. USP establishes written (documentary) and physical (reference) standards for medicines, food ingredients, dietary supplement products and ingredients. These standards are used by regulatory agencies and manufacturers to help to ensure that these products are of the appropriate identity, as well as strength, quality, purity, and consistency. Before sending out, we test these standards and it involves various techniques such as Ultra High Pressure Liquid Chromatography (UHPLC), High Performance Liquid Chromatography (HPLC), Differential Scanning Caloriemetry (DSC), Thermo gravimetric analysis (TGA), Inductive coupled plasma – optical emission spectroscopy (ICP-OES), High Performance Thin Layer Chromatography (HPTLC), Ultra-Violet Visible Spectroscopy (UV), Water Content analysis, Titration (Aqueous and Non-aqueous), Elemental analysis (Elementar and Thermo), Melting Range (Optimelt), Loss on Drying (LOD), Residue on Ignition (ROI), Specific Optical Rotation (SOR) and Infrared spectroscopy (IR). We also involved in IQ, OQ and PQ of equipments. We have worked under ISO 9001 and ISO 17025 certified lab. Our posted results were cross checked with other three collaborators. Show less

    • Novartis

      Mar 2016 - Jul 2022
      • Expert

        Sept 2021 - Jul 2022
      • Senior Scientist

        Mar 2016 - Sept 2021
    • Eli Lilly and Company

      Jul 2022 - now
      Senior Manager
  • Licenses & Certifications