Irene Körbl

Regulatory Affairs / Quality Assurance Manager at BAP Medical B.V.
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Location
Rijssen, Overijssel, Netherlands, NL

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Experience

    • Netherlands
    • Medical Equipment Manufacturing
    • 1 - 100 Employee
    • Regulatory Affairs / Quality Assurance Manager
      • Sep 2015 - Present

      Responsible for global product registrations (medical devices) and ISO13485 quality management system. Responsible for global product registrations (medical devices) and ISO13485 quality management system.

    • United Kingdom
    • Industrial Machinery Manufacturing
    • 700 & Above Employee
    • Coordinator Approvals
      • Sep 2008 - Aug 2015

      Responsible for global drinking water and food contact certification projects. Incl. Medical Device and legionella control certification. Quality Assurance ISO9001, auditing, complaints handling, improvement projects. Responsible for global drinking water and food contact certification projects. Incl. Medical Device and legionella control certification. Quality Assurance ISO9001, auditing, complaints handling, improvement projects.

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
      • Aug 2005 - Aug 2008

      Coordination of all registration activities of Puregon/Puregon Pen in Africa, Latin America, Asia, Pacific area and the Middle East.

      • Sep 1998 - Aug 2005

      Design and synthesis of pharmacological active compounds.

    • Netherlands
    • Chemical Manufacturing
    • 700 & Above Employee
    • Chemisch analyst
      • Sep 1997 - Aug 1998

      Development and improvement of water based coatings. Development and improvement of water based coatings.

    • Hospitals and Health Care
    • 1 - 100 Employee
    • Graduate student HLO
      • Sep 1996 - Jun 1997

Education

  • Saxion Hogeschool Enschede
    Ing., Organische chemie
    1993 - 1997

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