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Preclinical Quality Assurance

Development and management of audit strategies and programs for the Non-regulated drug discovery arena including:
- Determining audit strategies and risk evaluations
- Developing audit plans and system diagnostic tools
- Managing global audit programs including on outsourced activities
- Providing input on Good Research Practices
- Managing audit resource allocations
- Reporting out on audit findings
- Providing due diligence and for cause audit support
- Audits on preclinical data
- Audits on ESP
- Involved in GLP and GCLP audit strategies

Lab-, data- and project management


Current Experience

  • Ass. Director Quality Assurance non-regulated strategy Beerse, Belgium
    Since July 2013

Past Experience

  • Program Manager, Non-Regulated Quality Systems (R&DQA) Beerse, Belgium
    July 2012 --- June 2013

  • Data Manager Beerse, Belgium
    February 2008 --- June 2012

  • Senior Associate Scientist Beerse, Belgium
    February 1997 --- January 2008


Self Assessment :
Quality Assurance (QA)Quality AuditingQuality ManagementQuality SystemsQA complianceComplianceCancer ResearchLaboratory ResearchPre-clinical researchQualitative ResearchData ManagementPreclinical regulations and practicesTraining Labtechnician Cell biology BiochemistryLaboratory ManagementGood Laboratory Practice (GLP)oncologyDrug Discovery R&DGood Scientific Practicesgood research practicesPharmaceutical ResearchPharmaceutical SciencesPharmaceutical

Skills and Expertise

Self Assessment :
Control dataPeople managementCollaborate with project teamImplement Quality Management System (QMS)Conduct auditsFollow-up of external auditsFollow-up of internal auditsPrepare external auditsPrepare internal auditsRespond to audit findingsImplement Quality & Compliance strategyConduct research audits


  • Aggregaat in Secundair Onderwijs from University of Antwerp in 1997
  • Master in Biochemistry from University of Antwerp in 1997
  • Bachelor in Chemistry from Limburgs Universitair Centrum (Universiteit Hasselt) in 1994

Training and Certification

  • Implementing Good Clinical Laboratory Practice (GCLP) in 2015 Training
  • Frontline Leadership in 2012 Training
  • ISO31000 Risk Management in 2015 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Work Preferences

  • Locations I am interested in:
  • Work From Home:
    Yes, 0 to 1 days per week
  • Work Regime:
    Permanent position
  • International:

Area / Region



Driving License
  • Yes