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Validation Engineer Life Sciences (Flanders)

Your role

  • You will help define and support the Validation Approach,
  • You will establish procedures for Validation in accordance with international standards (FDA, EMA, ICH, ASTM E2500, GAMP),
  • You will write Validation documents (protocols, reports, SOPs, Critical Impact Assessments) and manage deviations,
  • You will coordinate and execute validation (IQ, OQ, PQ) tests,
  • You will perform risk assessments,
  • You will work in close collaboration with other departments for example production, engineering, maintenance, Quality Control, Quality Assurance…
  • You will ensure handover with final users.
  • Your profile

  • You hold a Master degree in Bio-, Chemical, or Pharmaceutical engineering or related scientific domains,
  • You are Native level of Dutch and fluent in English,
  • You have a first relevant experience in a GMP environment as a Validation, Qualification or Test Engineer,
  • You have Knowledge of the pharmaceutical industry, medical devices, biotech or Foodtech,
  • You are a natural communicator with negotiation skills.
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    Validation Engineer Life Sciences (Flanders)

    Company:
    Capgemini Engineering
    City:
    Brussels
    Contract type: 
    Permanent
    Categories: 
    Test And Validation Engineer
    Degree level: 
    Master
    Published:
    01.01.2022
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