Kripal Singh

Senior executive R&D API Synthesis at Ami Lifesciences Pvt. Ltd.
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Contact Information
us****@****om
(386) 825-5501
Location
Vadodara, Gujarat, India, IN

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Experience

    • India
    • Pharmaceutical Manufacturing
    • 200 - 300 Employee
    • Senior executive R&D API Synthesis
      • Mar 2021 - Present

      1.Literature search and its compilation2.To finalize the route of synthesis after doing feasibility study of ROS. 3.Develop the non infringing process for DMF and patentability.4.To develop cost effective, high quality and minimum environmental hazardous process following cGMP, & GLP guidelines.5.Lab process development its optimization and validation.6.Technology transfer from lab to pilot plant and PE Lab.7.To prepare the documents for PDR and DMF. 1.Literature search and its compilation2.To finalize the route of synthesis after doing feasibility study of ROS. 3.Develop the non infringing process for DMF and patentability.4.To develop cost effective, high quality and minimum environmental hazardous process following cGMP, & GLP guidelines.5.Lab process development its optimization and validation.6.Technology transfer from lab to pilot plant and PE Lab.7.To prepare the documents for PDR and DMF.

    • India
    • Pharmaceutical Manufacturing
    • 300 - 400 Employee
    • Executive
      • Apr 2020 - Mar 2021

      1. Literature search and its compilation2.To finalize the route of synthesis after doing feasibility study of ROS. 3.Develop the non infringing process for DMF and patentability.4.To develop cost effective, high quality and minimum environmental hazardous process following cGMP, & GLP guidelines.5.Lab process development its optimization and validation.6.Technology transfer from lab to pilot plant and PE Lab.7.To prepare the documents for PDR and DMF. 1. Literature search and its compilation2.To finalize the route of synthesis after doing feasibility study of ROS. 3.Develop the non infringing process for DMF and patentability.4.To develop cost effective, high quality and minimum environmental hazardous process following cGMP, & GLP guidelines.5.Lab process development its optimization and validation.6.Technology transfer from lab to pilot plant and PE Lab.7.To prepare the documents for PDR and DMF.

    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Scientist II
      • Oct 2016 - Feb 2020

      Reaearch & Development of API drugs Reaearch & Development of API drugs

    • India
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Research Associate
      • Apr 2015 - Sep 2016

      Process development and validation from lab to plant scale.Non infringing route development for API & intermediates.Literature search and patent searchTechnical support to analytical departmentCo-ordination with plant for tech transfer of newly developed productDocumentation of newly developed product Process development and validation from lab to plant scale.Non infringing route development for API & intermediates.Literature search and patent searchTechnical support to analytical departmentCo-ordination with plant for tech transfer of newly developed productDocumentation of newly developed product

Education

  • Maharaja Krishnakumarsinhji Bhavnagar University
    Master of Science, Organic Chemistry
    2012 - 2014
  • Saurashtra University, Rajkot
    Bachelor of Science - BS, Chemistry
    2009 - 2012

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