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Joshua Radke profile image

Joshua Radke

NA Quality Director & Global Quality Support at Fagron
Intro Book
Seasoned quality professional with 20+ years of experience in the pharmaceutical industry.
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Location
St Paul, Minnesota, United States, US
Skills
  • Chemistry
  • Pharmaceutical Industry
  • Gmp
  • Analytical Chemistry
  • Quality Control
  • Show all
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Bio

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Joshua Radke is a seasoned quality professional with 20+ years of experience in the pharmaceutical industry, holding a PhD in Chemistry from the University of Colorado Boulder. He has worked in various roles, including Quality Control Manager, Quality and Regulatory Affairs Manager, and Director of Analytical Chemistry/Quality Control. Radke has expertise in GMP, analytical chemistry, and quality assurance, with a strong background in organic and analytical chemistry. He currently serves as the NA Quality Director & Global Quality Support at Fagron, where he provides global quality information systems, supports quality continuous improvement projects, and manages technical transfer between sites of production for pharmaceutical products.

Experience

  • Fagron
    • Netherlands
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • NA Quality Director & Global Quality Support
      • May 2022 - Present

      Continuation of Sr. Specialist Duties with deepening responsibilities. Additional duties include global data governance quality support, global brand launch quality management, contract manufacturer quality management, and North America and global regulatory support.

    • Sr. North America Quality Specialist
      • Apr 2019 - Apr 2022

      Serve as a flexible resource for North American and global Fagron companies. Maintain global Quality information systems. Support and Manage Quality Continuous Improvement Projects for Fagron Companies. Support and manage technical transfer between sites of production for pharmaceutical products.

  • Fagron, Inc.
    • United States
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Quality and Regulatory Affairs Manager
      • May 2017 - Apr 2019

      Manage Quality Control and Quality Assurance Departments.

    • Quality Control Manager
      • Dec 2002 - Apr 2017

      Manager of Analytical Chemistry and Quality Control for cGMP regulated business.

  • Gallipot, Inc.
    • Director Analytical Chemistry/Quality Control/IT/IS
      • Dec 2002 - Aug 2010

      Director of Analytical Chemistry/Quality ControlDirector of all IT/IS for company. Responsible for Purchases, Deployment, Maintenance, and Software Development.In August, 2010, I was assigned to my degree focus (QC/Chemistry)

  • Univeristy of Colorado, Boulder
    • Boulder, CO
    • Research Assistant
      • 1995 - 2002
      • Boulder, CO

      Performed thesis research on a variety of topics including Organic Synthesis, Scanning Tunneling Electron Microscopy, Molecular Modeling, and ab initio Quantum Chemistry Calculations.

Education

  • 1994 - 2002
    University of Colorado Boulder
    PhD, Chemistry, Organic Chemistry, Computational Chemistry, Condensed Matter Physics
  • 1987 - 1994
    University of Minnesota
    BA, Chemistry, Chemistry

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Industry Focus. “Pharmaceutical and Healthcare”

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