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Validation Engineer - Life Sciences

Our offer

At Altran we value excellence, care, responsibility, dynamism and innovation. We offer a job with variation that leaves plenty of room for initiative and development. In fact, we are not just offering you a job, we’re inviting you to be part of our community where we will provide you trainings, tools & grounds for professional and personal growth.Each career experience is assorted by an attractive salary package.

If you are a team player, if you recognize yourself in this profile and are not afraid of taking on challenges… Apply today!

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, …)
  • You will manage deviations,
  • You will coordinate and execute validation (IQ, OQ, PQ) tests,
  • You will perform risk assessments,
  • You will work in close collaboration with production, engineering, maintenance, QC, QA…
  • You will ensure handover with final users.
  • Your profile

  • Master degree in engineering or related scientific domains,
  • Native level of French or Dutch and fluent in English,
  • At least 2 years of relevant experience in Validation in a GMP environment is mandatory
  • Knowledge of management (project/team management)
  • Validation Engineer - Life Sciences

    Altran, Brussels
    Categories: 
    Engineering
    Degree Level: 
    Master
    Apply before: