Position: Mid-Senior level

Job type: Full-time

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Job content

Tasks

  • Identify potential quality and compliance risks and help to manage these risks through the quality systems
  • Manage Deviations/CAPA
  • Manage the follow-up of SOP reviews
  • Review and/or approval of files and documents
  • Conduct and follow-up of internal or external audits

Benefits

  • Challenging projects based on your interests and skills
  • Personal follow-up and clear, transparent communication both before and after commencement of employment
  • Possibility to follow extra training
  • Inspiring network events and legendary after work drinks
  • Strong network of industry leading clients
  • Expertise within IT, Engineering and Life Sciences
  • A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees

Have you got what it takes?

  • Bachelor or Master’s degree with scientific orientation (biology, chemistry, chemical,) or relatable experience.
  • 1-5 years’ relevant experience in QA in a regulated environment (pharma, biotech) is a MUST
  • Good knowledge of GMP, Deviation, CAPA and Change control,
  • Autonomous, conscientious and positive problem-solving mindset.
  • Fluent in French and good level of English
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Deadline: 19-12-2025

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