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Summary

 

 


  • I am a chemical engineer who combines a strong technical background with the experience of working in a multicultural international environment.

  • I had operational and  project responsibilities and I built a sterile manufacturing site from a green field up to a running plant.

  • My strengths are a broad pharmaceutic technology knowledge, thorough understanding of GMP and regulatory demands, multicultural interest, ability to manage and motivate people under high workload conditions and tight deadlines, conceptual and results driven thinking.

  • My career objectives are an optimal contribution in an engineering/production management position in an international company by levering my pharmaceutical and multicultural experience.

  • Preferred functions are sterile manufacturing/cleanrooms focused or pharmaceutics in general in different disciplines like Product Support / Process & Equipment / Technology Transfer / Commissioning & Validation / Project Engineering / Consultancy. Examples are: Production Manager, Engineering Manager, Validation Manager, Project Manager, Consultant.

 

Experiences

Current Experience

  • Manager Clinical Supplies,
    Since June 2012

    Production of test kits for Clinical Trials, Technology Transfer and Validation/Engineering Projects.

Past Experience

  • Senior Production Manager
    September 2008 --- May 2012
    Design, construction, commissioning, validation & start-up of a new production facility of sterile eye drops in Singapore, starting from a green field to commercial production.

  • Production Manager
    May 2008 --- September 2008
    Production of sterile eyedrops

  • Production Supervisor
    October 1988 --- May 2008
    Production of sterile eyedrops. Trouble shooting. Tech Transfer / PSBs / Qualification / Validation JIT scheduling

  • Production Leader
    June 1985 --- October 1988
    Responsible for the production 24/7 of gelatine capsules.

  • Production Supervisor Assistant
    September 1980 --- June 1985
    Responsible for the production of non-sterile pharmaceutics: granulation, tabletting and coating, capsule filling, cream and ointments, syrups and shampoos, inhalators, packaging.

Personality

Self Assessment :
Analytical thinkingSociabilityStrategic thinkingSelf-confidenceProblem solvingInterest in knowledgeIndependenceFlexibilityCoordinationOptimism

Knowledge

LinkedIn Assessment :
Specialist Sterile Production PharmaceuticsSpecialist Aseptic Techniques & Processespeople managementmanagementCross-functional team leadershipPharmaceuticsManufacturingAseptic ProcessingScuba DivingValidationProject ManagementTechnology transferProcess EngineeringGMPCAPAFDASOPRegulatory affairsChemistryQuality Assurance (QA)GXPV&VChange ControlQuality Systems21 CFR Part 11Pharmaceutical IndustryClinical trialsSterilizationMedical Devices

Skills and Expertise

Self Assessment :
Create SOPs Develop protocols Technology researchAdjust processes and methodsAssure medical qualityCoachPilot scale batchesSolve problems

Education

  • Functional Analist in Computer Science from University Leuven in 1985
  • Master of Science in Chemical Engineering from Hoger Instituut De Nayer in 1978
  • Technician in Pharmaceutic Chemistry from Technische Scholen Mechelen in 1973

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
English
Full Proficiency
French
Elementary Proficiency
German
Elementary Proficiency

Work Preferences

  • Work From Home:
    Yes, 0 to 2 days per week
  • Work Regime:
    Permanent position
  • International:
    Yes

Area / Region

Keerbergen, België

Others

Driving License
  • No