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Current Experience

  • Production Support - Finishing Production Department - Consultant for The Biotech Quality Group

    Since August 2015
    Consultant for the biotech quality group role and responsabilities : - Change Control writing/management - deviation and action plan writing/management - Troubleshooting and coordination - continuous improvement project initiation/management Consultant for the Biotech Quality Group Role and Responsabilities : - Change control writing/management - Deviation and action plan writing/management - Troubleshooting and coordination - Continuous Improvement project initiation/management

  • Consultant

    Since March 2014

Past Experience

  • Quality Support - Change Management - Consultant for The Biotech Quality Group

    May 2015 --- August 2015
    Consultant for the biotech quality group role and responsabilities Change Control: - review and approval of Change Control at different process step - ensure following of change from initiation through different steps - ensure quality support for Change Management improvement - analyse and evaluate the Change Control management process - propose and implement potential improvement

  • Quality Support - Raw Material Release - Consultant for The Biotech Quality Group

    March 2015 --- April 2015
    Consultant for the biotech quality group roles and responsibilities: deviation - investigations (within trackwise 8 system) - identification and creation of useful action plans projects and Change Control - closure of supplier Change Control - lead of several projects (specification & procedure update, team organization) - redaction of guidance and Training for “new practices” - support for routine work

  • Quality Support - Deviation Process

    September 2014 --- March 2015
    Consultant for the biotech quality group on cGMP improvement project - diagnose and improve the deviation process, - investigate and write deviation reports, - define adapted capas.

  • QA Officer - QA Pharma Manufacturing - Dry Forms

    March 2014 --- August 2014
    Consultant for the biotech quality group role and responsabilities deviation & capa - investigations on several deviations to found the most probably root cause - qa review of process and documental deviation - propose and find possible capa to avoid recurrence - follow-up and review of capas and action plans Validation - Validation of new dp and new api’s supplier - review of Validation documents: quality risk Analysis (qra), process performance quality science)" rel="nofollow">Protocol (ppqp), process design development (pdd) - review of master batch record - qa follow-up of the projects in accordance to the cGMP tech transfer - authorization of tech transfer towards Manufacturing - review and approbation oftech transfer science)" rel="nofollow">Protocol, tech transfer report release - review of master batch records and specifications - writting, review and follow-up of product quality review others - follow-up of ra commitments - act as back up for other team qa officers and assistants according to manager instructions - assist manager to achieve team objectives

  • Research Associate - Master graduate

    February 2013 --- July 2013
    synthesis of molecules as inhibitors of a protein involved in epigenetic therapy role and responsabilities - optimization of a synthesis pathway, from a literature of the 70's - study of the effects of different substituents on the target's activity - following of conversion and Characterization of structures thanks to available Analytical methods (hp-lc, up-lc, LC-MS, GC-MS, NMR proton, carbon and 2d) - different ways of Purification used : flash Chromatography (normal and reverse phase), manual column, prep. tlc - types of reactions : heterocyclic Chemistry (fisher indolisation, cyclisations, ...), pallado-catalyzed reactions (sonogashira, pd/c deshydrogenation, buchwald coupling), cyclisation (diels-alder, ...) - softwares used : acd Lab for NMR Analysis, chemdraw as Molecule drawer, 3d chemdraw for enthalpy calculation, pymol for Molecule-protein Interactions, ms (word, Excel, PowerPoint) for Presentations, reports, eln (electronic Lab notebook)

  • Research associate

    February 2012 --- August 2012
    internship synthesis of Alzheimer's disease target molecules

  • Intern

    August 2011 --- January 2012
    synthesis of novel fungicide molecules - Organic Synthesis - Analytics used : HPLC, LC-MS, GC-MS, c-and h- NMR - purifications : combi flash column and reverse phase column

  • Intern

    April 2011 --- May 2011
    - study of mineralization of diuron by a consortium of Bacteria - decontamination of vineyards' soils - sterile cultivation of Bacteria - dosage of the minaralizetion of diuron by HPLC


LinkedIn Assessment :
ChemistryPharmaceutical ManufacturingAnalytical ChemistryOrganic ChemistryMulti-step SynthesisGMPR&DGood Laboratory Practice (GLP)Pharmaceutical IndustryTechnical TransfersProcess ValidationQC ToolsTrackwiseSAPLIMSProduct SpecificationFDA GMPDeviation ManagementCAPARegulatory affairsRoot Cause AnalysisAction Plan DevelopmentSOPQuality OperationsGood Distribution Practice (GDP)Analytical Methods DevelopmentSupplier QualityPharmaceutical ConsultingCorrective ActionsVisual InspectionProduct QualityChange ManagementSecteur pharmaceutiqueBPFChimie


  • Ingeneer Diploma in Organic, Bioorganic and Therapeutic Chemistry from Ecole Nationale Superieure de Chimie de Mulhouse in 2013
  • Master of Research degree in Organic Synthesis from Université de Haute-Alsace Mulhouse-Colmar in 2013
  • Licence 2 in Physic Chemistry from CPGE Dumont d'Urville (Toulon) Physique-Chimie in 2009

Area / Region

Brussels, Belgium


Driving License
  • No

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