Site QA Director (m/f/d).

Job ID: 11357

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Type of employment
  • Ensure all products and materials released from the manufacturing site adheres to international compliance standards
  • Responsible for leading a QA organisation in the areas of:
    • QMS
    • Product certification and Releases
    • QA budget and forecasts as well as reaching set targets
  • Complete regular administration reviews on the QMS with the Site Management Team and manage all Regulatory Body inspections and audits

  • Responsible to identify site quality policy and implementation within the facility

  • Responsible for the overall quality of finished products being released to the US and European market

  • Responsible for creating the QA departments budgets and reaching site targets

  • University degree in Science
  • Excellent command of the English language, written and oral
  • Sound knowledge of the pharmaceutical industry with GMP and QMS
  • Experience in working in a highly-matrix organisation
  • Experienced in implementing change-management methodologies and continuous improvement to a department in a manufacturing facility
  • Leadership experience working with a management system of according to ISO 9001 and ISO 13485