Daphne BIJLSMA

Head of Product Verification and Validation and Technology Transfer at Quotient Limited
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Contact Information
us****@****om
(386) 825-5501
Location
Eysins, Vaud, Switzerland, CH
Languages
  • French Native or bilingual proficiency
  • English Professional working proficiency
  • Dutch Native or bilingual proficiency

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Experience

    • Switzerland
    • Medical Device
    • 100 - 200 Employee
    • Head of Product Verification and Validation and Technology Transfer
      • Feb 2020 - Present

    • Product Verification and Validation Manager
      • Sep 2018 - Feb 2020

    • Instrument Validation Engineer
      • Jul 2016 - Sep 2018

  • Pictor Limited
    • Auckland, New Zealand
    • Scientist
      • Apr 2016 - Jun 2016

      Pictor Limited develops and commercializes a technology for multiplexed testing of blood and other biological fluids. Responsibilities: - Development of biological immunoassays - Statistical evaluation of data quality. - Documenting daily activities, protocols and data Pictor Limited develops and commercializes a technology for multiplexed testing of blood and other biological fluids. Responsibilities: - Development of biological immunoassays - Statistical evaluation of data quality. - Documenting daily activities, protocols and data

    • France
    • Medical Equipment Manufacturing
    • 200 - 300 Employee
    • Project Manager- Biomedical Engineer In Vitro Diagnostics
      • Dec 2011 - Jul 2015

      Project management and team coordination - Development and validation of reagents on analyzers - Project planning and follow-up - Evaluation of resources and cost management - Industrialization of processes - Inter-office coordination: marketing, quality assurance, regulatory affairs, production - Reporting Instrumentation - Maintenance of analyzers: Selectra Pro Series/ Envoy500 & Eon100/300 - Knowledge of instrument qualification and validation: IQ, OQ, PQ Regulatory Affairs - Quality management - GMP/GLP guidelines, ISO 13485, ISO 9001, ISO 17025 and 21CFR820 norms -Participation in the elaboration of technical files for registration of medical devices in compliance with european and international procedures ( CE / FDA ( 510K ) ) - Risk assessment Show less

    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • R&D Engineer Assistant
      • Jan 2010 - Oct 2010

      Creation and optimization of a new device based on TRACE Technology (Time Resolved Amplified Cryptate Emission) Drafting of protocols Antibody purification Creation and optimization of a new device based on TRACE Technology (Time Resolved Amplified Cryptate Emission) Drafting of protocols Antibody purification

    • R&D TECHNICIAN
      • Apr 2009 - Jul 2009

      Study of the role of NOX2 in aging and associated diseases by using a transgenic animal model (mouse). Animal care and breeding (cleaning cage, feeding, monitoring , collecting data,…) Rotarod performance tests on mice in order to assess their coordination and endurance according to their genotype Optimization of scientific protocols for screening lipid peroxidation (TBARS) Cells quantification with Flow cytometry Western Blotting Bibliography research Study of the role of NOX2 in aging and associated diseases by using a transgenic animal model (mouse). Animal care and breeding (cleaning cage, feeding, monitoring , collecting data,…) Rotarod performance tests on mice in order to assess their coordination and endurance according to their genotype Optimization of scientific protocols for screening lipid peroxidation (TBARS) Cells quantification with Flow cytometry Western Blotting Bibliography research

Education

  • Ecole de Biotechnologies, Grenoble
    Master 2 (M2) Industry of the In Vitro Diagnostics, Biotechnology
    2008 - 2010
  • University Joseph Fourier
    Bachelor's degree, Biology
    2006 - 2008

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