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Experiences

Current Experience

  • Senior Clinical Developer


    Since January 2009
    final responsible for set-up, co-ordination and managing of analytical and Clinical performance activities (internal and external) in view of targeted registration requirements (ce, FDA and Health canada) of Nucleic acid and/or Protein based quantitative or qualitative In Vitro Diagnostic Assays. Final responsible for set-up, co-ordination and managing of analytical and clinical performance activities (internal and external) in view of targeted registration requirements (CE, FDA and Health Canada) of nucleic acid and/or protein based quantitative or qualitative in vitro diagnostic assays.

Past Experience

Knowledge

LinkedIn Assessment :
Laboratory SkillsProduct developmentClinical DevelopmentRegulatory RequirementsProject ManagementSequencingAssay developmentPCRValidationBiotechnologymolecular biologyMolecular DiagnosticsData AnalysisRegulatory affairsDNALifesciencesLife SciencesFDAIn VitroImmunology

Education

  • in from in 1995

Area / Region

Beervelde, Lochristi, Belgium

Others

Driving License
  • Yes

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