水平: Entry level

工作类型: Full-time

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工作内容

  • Review and write Validation documentations, plans and reports
  • Plan, organize and manage Validation activities
  • Review and monitor change control
  • Identify and solve problems

What are we looking for?

  • Bachelor or Master’s degree with scientific orientation or relatable experience
  • 1-5 years of experience in Validation (Process Validation/CSV/Method Validation) within the pharmaceutical industry
  • Experience in cleaning validation is a plus
  • Good knowledge of GMP regulations
  • Autonomous, conscientious, and positive problem-solving mindset.
  • Fluent in French and good level of English

What do we offer?

  • 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
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最后期限: 09-01-2026

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