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Summary

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

Experiences

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

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

Knowledge

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

Education

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

Languages

BrightOwl Assessment:
Self Assessment:
French
Native
English
Professional Proficiency

Area / Region

Andenne, Belgique

Others

Driving License
  • Yes