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Experiences

Past Experience

  • Compliance and regulatory expert

    June 2014 --- April 2015

    Project Management (implémentation of new processes)

    coordination

    Training

    drafting SOP

    international / across departments

    improve Treatment and transfert of key informations/documents between regulatory department and Operations 

Personality

Self Assessment :
AdaptabilityAttention to detailCoordinationOrganization

Knowledge

Self Assessment :
NegotiationAuditingCAPAChange ControlCMCCurrent Good Manufacturing Practice (CGMP)Good Distribution Practice (GDP)ICH guidelinesImmunoassaysImmunocytochemistry (ICC)ISO 9001LIMSLinuxMicrosoft ExcelMicrosoft OfficeMicrosoft PowerpointMicrosoft WordOutlookPackagingPharmaceutical ManufacturingpharmacologyProcess improvementProcurementProject CoordinationQA complianceQuality AuditingQuality Assurance (QA)Quality Management System (QMS)Regulatory ComplianceRoot Cause Analysis (RCA)Sterile drug productsTraining

Education

  • Advanced Master in Pharmaceutical products and health products from Université de Bourgogne in 2010

Languages

BrightOwl Assessment:
Self Assessment:
French
Native
Spanish
Native
English
Full Proficiency
Portuguese
Professional Proficiency
Arabic
Professional Proficiency
Russian
Elementary Proficiency
Polish
Elementary Proficiency
Dutch
Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Qualified Person Quality Engineer Quality manager Compliance Manager Expert
  • Locations I am interested in:
    Belgium
  • Work From Home:
    No
  • Work Regime:
    Permanent position :    100% FTE
    BrightOwl employee :    100% FTE
  • International:
    No

Area / Region

Brussels, Belgium

Others

Driving License
  • Yes

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