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Experiences

Current Experience

  • Global Quality & Risk Senior Manager

    Zaventem, Belgium
    Since March 2016

  • Global QA Supplier Quality Shared Services - Suppliers Manager


    Since January 2009
    manage quality and data of the bio process stream suppliers: •lead, manage and/or support GMP world wide audits of gsk Biological third parties for Qualification, GMP monitoring, target audit •follow-up of suppliers capa plans •manage supplier quality evaluation for the bio process portfolio •initiate quality agreements for key suppliers •initiate supplier improvement / development programs •use scientific and technical know how for supporting global quality related deviations with global suppliers •create and maintain supplier and raw mat data base for the bio process portfolio Manage quality and data of the Bio Process stream suppliers: •Lead, Manage and/or support GMP world wide audits of GSK Biological third parties for qualification, GMP monitoring, target audit •Follow-up of suppliers CAPA plans •Manage supplier quality evaluation for the Bio Process portfolio •Initiate Quality Agreements for key suppliers •Initiate supplier improvement / development programs •Use scientific and technical know how for supporting global quality related deviations with global suppliers •Create and maintain supplier and raw mat data base for the Bio Process portfolio

Past Experience

  • QA Training & Documentation Coordinator

    October 2006 --- December 2010
    Training and Documentation management within qa team. part of Training editorial team. GMP and Auditor Trainer.

  • ISO 9000 Lead Auditor at BQAgie

    January 2000 --- January 2006

  • Quality & Certification Coordinator

    January 2000 --- January 2005

  • Toxicologist

    September 1988 --- January 1990

Knowledge

LinkedIn Assessment :
GMPCAPAQuality Assurance (QA)Quality SystemsPharmaceutical IndustryISOBiotechnologyVaccinesQuality AuditingChange Control21 CFR Part 11AuditingBiopharmaceuticalsQuality ManagementGXPQuality SystemsAseptic ProcessingISO 9000PharmaceuticsGCPcGMPSupplier Qualitysupplier auditscGMP practicesInvestigationDisposablesSingle used technologyRegulatory ComplianceFDAregulatory inspection

Education

  • in Toxicology from Université catholique de Louvain in 1990

Area / Region

Belgium

Others

Driving License
  • Yes

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