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Experiences

Current Experience

  • Head of Regulatory Bioanalysis


    Since September 2015
    i am accountable for all in-house regulatory bioanalytical activities conducted by ucb. i work with a team of scientists developing and validating bioanalytical methods and conducting subsequent sample Analysis. we develop methods for both Small molecules by LC-MS/ms or large molecules by either LC-MS/ms, ligand binding assay or hybrid approaches. I am accountable for all in-house regulatory bioanalytical activities conducted by UCB. I work with a team of scientists developing and validating bioanalytical methods and conducting subsequent sample analysis. We develop methods for both small molecules by LC-MS/MS or large molecules by either LC-MS/MS, Ligand Binding Assay or hybrid approaches.

  • Senior Principal Scientist Bioanalysis


    Since September 2011
    i am in charge of a team of technicians, my main task is to develop and validate bioanalytical methods supporting drug develoment. I am in charge of a team of technicians, my main task is to develop and validate bioanalytical methods supporting drug develoment.

Past Experience

  • Principal Scientist Bioanalysis

    July 2008 --- September 2011
    i am in charge of a team of technicians, my main task is to develop and validate bioanalytical methods supporting drug develoment.

  • Senior Research Scientist Bioanalysis

    March 2008 --- July 2008

  • Research Scientist Bionanalysis

    March 2005 --- March 2008

  • PhD student

    August 2000 --- February 2005

Knowledge

LinkedIn Assessment :
LC-MSMass SpectrometryBioanalysisDMPKHPLCChromatographyAnalytical ChemistryValidationGLPDrug DevelopmentDrug DiscoveryDrug metabolismPharmacokineticsLife SciencesADMEGood Laboratory Practice (GLP)ChemistryHigh-Performance Liquid Chromatography (HPLC)BiotechnologyPharmaceutical Industry

Skills and Expertise

Self Assessment :
Create SOPs Write protocolsAnalyze proteinCollaborate with principal investigatorCreate study documentsEnsure data integrityFollow-up of Quality Management System (QMS) processesGuide staffInteract with pre-clinical scientistsInterpret analytical resultsInterpret scientific dataLead teamsSupervise analysts and researchersLC-MS/MSLigand Binding AssayRegulatory Bioanalysis

Education

  • PhD in Pharmaceutical Sciences in Pharmacy from Ghent University in 2005
  • Industrial Pharmacy in Pharmacy from Ghent University in 2000
  • Pharmacist in Pharmacy from Ghent University in 1999

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
English
Full Proficiency
French
Full Proficiency
German
Elementary Proficiency

Work Preferences

  • Notice Period:
    13 weeks
  • Locations I am interested in:
    Belgium
  • Work From Home:
    No
  • Work Regime:
    Permanent position :    100% FTE
  • International:
    No

Area / Region

Merelbeke, Belgium

Others

Driving License
  • Yes

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