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european/american (FDA) regulations in Food contact, reach, clp, SAP, Quality Assurance (capa), msds, ehs, Auditor, Planning, scheduling, lean, 6 sigma, green belt, dmaic, GMP, continuous improvement


Current Experience

  • Expert consultant

    Since February 2014
    on assignment with gsk: - environmental invalid tests reduction role: pmo - task force backlog déviation / capa reduction roles : déviation manager / deviation writer On assignment with GSK: - Environmental invalid tests reduction Role: PMO - Task force backlog déviation / CAPA reduction Roles : Déviation manager / deviation writer

Past Experience

  • Green Belt

    December 2012 --- February 2014
    application of the dmaic methodology, use of lean-6sigma tools (kanban, 5S, etc.), project Leadership ie extruders throughput optimization in powder production area by 20%

  • Production planner / Material management officer

    October 2011 --- February 2014
    Analysis of raw material needs, Planning of customer orders (sch++), coordination of current productions (sch++ & frozen zone), Analysis and optimization of the inventories (stocks, slow movers), coordination of meetings for departments "Supply Chain" / "production" / “Customer Service” (Sales & Operations meetings)

  • Regulatory Product Stewardship France-Benelux

    February 2006 --- November 2012
    department regulatory product stewardship france-benelux, responsible for 3 team members, management of database in SAP, creation of msds, build up reach registration dossier, key contact for clp/ghs, key contact for transportation classification (imds, iata, adr), monitoring and enforcement regulation (Food contact certificates, national laws, pharmacopea, implementation of reach directive), Training operational people

  • Head of Product Safety & Regulatory Affairs

    April 2008 --- January 2011

  • Country System Manager / Quality Assurance Manager

    September 2006 --- March 2009
    management and Planning of internal quality audits, implementation of standards ISO 9001:2008, iso 14001:2004, ohsas 18001 :2008, management of customer complaints and internal complaints (via SAP): records, implementation and monitoring of corrective / preventive actions (capa), coordinate monthly Presentations of results to management (Statistics, monitoring of kpi's), maintenance, improvement and harmonization of Quality Management systems in the benelux region, implementation of the goals / objectives in local regional projects, reporting of results at european level, organization of external audits


LinkedIn Assessment :
GMPISO 14001ISO 9000Quality Assurance (QA)Quality AuditingQuality SystemsSupply ChainSix SigmaSAPPlasticsProduct StewardshipLean Manufacturing


  • Bio-Engineer in Phytopathology from Université catholique de Louvain in 2005
  • Science in Physics, Chemistry from Collège Ste Marie (Mouscron) in 2000


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Area / Region

Andenne, Belgique


Driving License
  • Yes

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