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CSV Engineer - Life Sciences

Your role

Key responsibilities

  • Review and analyze CSV parts from our client;
  • Realize on field Gemba in order to check the conformity of the project and recommendation;
  • Take Corrective Action / Preventive Action regarding CSV aspects;
  • Be a guide for our client regarding regulatory compliance and computer validation;
  • Assure the link between Altran and the client regarding all CSV aspect.
  • Your profile

    You are an “Innovation Maker” and you want to put your engineering , science and business skills to use to create solutions. You like to share your knowledge with likeminded engineers and you know how to take initiative .

    You have:

  • Master degree in (Bio-)engineering, computer science or related domains,
  • Fluent in English and French or Dutch,
  • At least 3 years of relevant experience in CSV in a pharmaceutical industry (as FDA part 11);
  • You will be recruited by Georges & Isabelle, don’t hesitate to contact them & send them your CV: -

    Discover more about your career on

    CSV Engineer - Life Sciences

    Altran, Brussels
    Degree Level: 
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