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project and Product Manager / product support Engineer / Trainer core competencies: project and Product management, studies Coordinator, transfusion and Medical Device knowledge, science)" >Protocol/Report Writing, monitoring studies, Data Analysis, Trainer, beam experience (gamma and electrons), PCR, Purification, Sequencing, Microbiology (In Vitro, In Vivo culture and transplantation). social skills: result oriented, positive minded, team player, flexible, persevering, rigorous and diplomatic.


Current Experience

  • International Product Manager

    Since August 2013
    scientific support to the exclusive agents of the various countries. benmarking and Competitive Analysis. development of argumentation. elaboration of products brochures for pediatricians. Training courses abroard for the medical representatives of our agents. scientific support to our agents from the corporate office and abroad in the field. Scientific support to the Exclusive Agents of the various countries. Benmarking and competitive analysis. Development of argumentation. Elaboration of products brochures for pediatricians. Training courses abroard for the Medical Representatives of our agents. Scientific support to our agents from the corporate office and abroad in the field.

Past Experience

  • Product Support Engineer & Product Support Specialist

    November 2007 --- July 2013
    as product support Engineer: • support product developments or enhancements. this includes the development of design control protocols, executing the studies and producing reports. • collaboration with external suppliers and the Manufacturing plants required. • run post Marketing studies on new or upgraded devices. as product support specialist: • lead the implementation support activities sustaining deployment of a red Cell collection apheresis platform (alyx) in key accounts selected throughout europe. • network the clin ed specialists identified within countries to support alyx implementation. • prepare and deliver Training programs to country clin ed specialists or distributors. • coordinate with team the implementation of new launched Software including cer protocols. • elevate customer issues (quality, supply, product features...) and track resolution.

  • Manager First Spin-off

    October 2003 --- September 2007
    management of a first spin-off developing a new Treatment by ionization to improve wood durability: benchmarking and Competitive Analysis, network setup, prospecting, collaboration with centers and companies, international conferences, Advertising in various trade fairs, design analysis, Process development, Publications and reports.

  • Project Researcher (Xylowall)

    September 2001 --- August 2003
    development of a new Treatment by ionization to improve wood durability: Research towards optimal Treatment for wood.


Self Assessment :
AdaptabilityCollaborationInterest in knowledgeCoordinationFlexibilityOptimismSociabilityOrganization


Self Assessment :
Medical devices R&D Scientific writingEnglish Cell biologyCell biologyCell CultureClinical monitoringClinical Study DesignClinical study reportsCommunication SkillsData AnalysisData cleaningData entryData ManagementDNA extractionDNA sequencingElectronic Data Capture (EDC) FDAGood Laboratory Practice (GLP)Good Manufacturing Practice (GMP)ICH GCP guidelinesIn VitroMedical affairsMedical DevicesMicrosoft ExcelMicrosoft OfficeMicroscopyMonitoring Study ProgressPCRPowerPointProduct designProject ManagementProtocolQuality Assurance (QA)R&DScientific WritingSerious Adverse Event (SAE)SOPTechnical reportsValidationWriting Study Procedures and SOPs
LinkedIn Assessment :
Medical DevicesQuality SystemsValidationGMPProcess improvementQuality Assurance (QA)Product managementISO 13485Good Laboratory Practice (GLP)Product developmentTrainersDesign ControlProduct launchR&DCompetitive Analysis

Skills and Expertise

Self Assessment :
Analyze data Design case record forms Develop protocols Interact with nurses Guide students Report dataCommunicate with investigatorConduct post-marketing surveillance studycoordinating research projectsExecute scientific projectsOral presentationOrganise meetingsPresent data at congressProvide trainingReport dataSearch literature on clinical trialsSupervise techniciansVerify dataValidate dataWrite protocols


  • Master in management in from IAG Louvain-la-Neuve in 2005
  • Engineer's degree in Bio-engineer from Université catholique de Louvain in 1998

Training and Certification

  • Learning facilitator, Inter-ActiveMinds in 2012 Training
  • Transfusion knowledge, INTS, Paris in 2010 Training
  • Biology introduction, INTS, Paris in 2008 Training
  • CE Medical Device Conformity, BioWin in 2008 Training
  • Good Laboratory Practice, BioWin in 2008 Training
  • Clinical Research Associate, BioWin in 2007 Training
  • Introduction to ISO and Good Manufacturing Practice, Pragmagora Society in 2006 Training
  • Certified animator in 1992 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Elementary Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Locations I am interested in:
    Braine-l'Alleud, Belgium Charleroi, Belgium Fleurus, Belgium Gembloux, Belgium Genappe, Belgium Gosselies, Charleroi, Belgium Louvain-la-Neuve, Ottignies-Louvain-la-Neuve, Belgium Mont-Saint-Guibert, Belgium Namur, Belgium Ottignies-Louvain-la-Neuve, Belgium Waterloo, Belgium Wavre, Belgium
  • Work From Home:
  • Work Regime:
    Permanent position :    80 to 100% FTE
    BrightOwl employee :    80 to 100% FTE
  • International:

Area / Region

Marbais, Villers-la-Ville, Belgium


Driving License
  • Yes

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