kim de Ruiter

Validation Technician at Byondis
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Contact Information
us****@****om
(386) 825-5501
Location
Arnhem-Nijmegen Region, NL
Languages
  • Nederlands Native or bilingual proficiency
  • Engels -

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Experience

    • Netherlands
    • Pharmaceutical Manufacturing
    • 200 - 300 Employee
    • Validation Technician
      • Apr 2020 - Present

    • Netherlands
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Maintenance & validation technician
      • Jun 2016 - Apr 2020

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • scientist , preclinical Development
      • 2011 - Jan 2015

      - Analytical support (performing, reporting and verification of analytical methods). - Writing and reviewing analytical protocols and reports. - Development and validation of HPLC methods. - Manager HPLC systems (Troubleshooting, maintenance and qualification) - Manager GMP reference standards - Deviations ( equipment related issues) - Analytical support (performing, reporting and verification of analytical methods). - Writing and reviewing analytical protocols and reports. - Development and validation of HPLC methods. - Manager HPLC systems (Troubleshooting, maintenance and qualification) - Manager GMP reference standards - Deviations ( equipment related issues)

    • Validation Engineer / Lab. support technician
      • 2009 - 2011

      - Managing investments for the purchase of new equipment (writing VP,URS, GQP and VR documents) - Managing en coordinating equipment projects (IQ/OQ/PQ) - Validation, calibrating and control of analytical equipment - Troubleshooting and performing repairs on HPLC equipment - Verification of GMP documentation - Manager of lab consumables (HPLC colums, GMP reference standards, chemicals) - Managing investments for the purchase of new equipment (writing VP,URS, GQP and VR documents) - Managing en coordinating equipment projects (IQ/OQ/PQ) - Validation, calibrating and control of analytical equipment - Troubleshooting and performing repairs on HPLC equipment - Verification of GMP documentation - Manager of lab consumables (HPLC colums, GMP reference standards, chemicals)

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Pharmaceutical laboratory assistent
      • 2007 - 2009

      -Stability research of new pharmaceutical formulations in GMP environment -Analytical method development and validation (HPLC) -Data verification -Stability research of new pharmaceutical formulations in GMP environment -Analytical method development and validation (HPLC) -Data verification

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Quality Control laboratory assistent
      • 2000 - 2006

      - Quality control analyses in a GMP environment (HPLC, GC, Dissolution) - Stability analysis - Verification of analysis - Quality control analyses in a GMP environment (HPLC, GC, Dissolution) - Stability analysis - Verification of analysis

Education

  • Hogeschool van Arnhem en Nijmegen
    Bachelor of Science (B.S.), Analytische chemie
    1996 - 2000
  • Nijmegen west
    HAVO
    1991 - 1996

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