Paul Koevoets

Director Analytical Chemistry at Vico Therapeutics B.V.
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Contact Information
us****@****om
(386) 825-5501
Location
Amsterdam, North Holland, Netherlands, NL

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Experience

    • Netherlands
    • Biotechnology Research
    • 1 - 100 Employee
    • Director Analytical Chemistry
      • Mar 2020 - Present

    • Netherlands
    • Biotechnology Research
    • 100 - 200 Employee
    • Senior Scientist CMC
      • Mar 2019 - Mar 2020

      Analytical method development in the ultra rare disease area:- Supervision of internal and external analytical development and quality control projects.- Analytical development and validation of purity and assay method for oligonucleotides.- LC-UV-MS method development and -validation Analytical method development in the ultra rare disease area:- Supervision of internal and external analytical development and quality control projects.- Analytical development and validation of purity and assay method for oligonucleotides.- LC-UV-MS method development and -validation

    • Scientist
      • Aug 2008 - Mar 2019

      -Development and qualification of (bio-) analytical methods suitable for GMP/GLP quality systems.- UPLC-MS techniques.-Documentation of the work in reports.-Presenting the work, also in external conferences and workshops.-Coordination of method development in a team.-Training on the job -Development and qualification of (bio-) analytical methods suitable for GMP/GLP quality systems.- UPLC-MS techniques.-Documentation of the work in reports.-Presenting the work, also in external conferences and workshops.-Coordination of method development in a team.-Training on the job

    • Senior Research Assistant
      • Aug 2008 - Mar 2019

    • Biotechnology Research
    • 400 - 500 Employee
    • Senior Research Assistant
      • Jan 2004 - Aug 2008

      -Development of QC analyses in bio pharmaceutical product development.-HPLC-UV-MS techniques.-Peptide mapping, protein purification, protein aggregation.-Documentation of the work in reports and SOP's. -Development of QC analyses in bio pharmaceutical product development.-HPLC-UV-MS techniques.-Peptide mapping, protein purification, protein aggregation.-Documentation of the work in reports and SOP's.

    • Netherlands
    • Biotechnology
    • 1 - 100 Employee
    • Senior Research Assistant
      • Oct 2001 - Dec 2003

      -Development of drug discovery screening methods, using HPLC-MS- and HPLC-biochemical detection.-Documentation of the work in reports and SOP's. -Development of drug discovery screening methods, using HPLC-MS- and HPLC-biochemical detection.-Documentation of the work in reports and SOP's.

    • Netherlands
    • Higher Education
    • 700 & Above Employee
    • Biochemisch analist
      • 1986 - 1999

Education

  • Dr. Struycken-Instituut, Etten-Leur
    HBO biochemisch-analist (HNWO), ing
    1981 - 1985
  • Dr. Struycken Instituut, Etten-Leur
    HBO A, klinisch chemisch hematologisch analist, ing
    1977 - 1981

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