Quality Assurance Engineer/Consultant

☞ Altran

Visualizza: 135

Giorno di aggiornamento: 26-11-2025

Località: Antwerp City Antwerp

Categoria: Produzione / Funzionamento

Industria:

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Contenuto del lavoro

Currently we are offering a specific position in our Life Sciences division with a lot of variation and focused on taking initiative and your professional development. This project within Quality Assurance consists of activities close to various topics like Deviations, Change Control, CAPA, Batch Releases, Qualification, etc. We make sure that this project continues to build on your current experience and exposes you to new inspiring domains. If you recognize the next move of your career in this job offering, we look forward to discovering together with you how much of a match you are to the requirements. With this project we launch your Capgemini Engineering career and we invite you to become a part of our Capgemini Engineering community. In this community we organize trainings, share unforgettable experiences, offer a variety of development tools and tons of possibilities to develop yourself as a professional and as a person. All of our career opportunities are accompanied by an attractive salary package.

If you are a team player, you recognize yourself in this profile and you are up to the challenge… Send us your resume today!

Your role

  • You are responsible for complaint handling, change control, deviations, CAPA, etc;
  • You ensure the compliance to standards (FDA, EMA, ICH, ISO,…);
  • You take on the QA Qualification of equipment, facilities and utilities;
  • You create the Product Quality Reviews (PQR) and the Continued Process Verifications (CPV);
  • You take on the role as project manager within the QA department and make sure of the follow-up on all aspects;
  • You are responsible for the follow-up of operational QA during production or distribution of supplies;
  • You manage the planning and execution of internal audits;
  • You are the trainer for all GMP related topics within the department of the client.

Your profile

  • Master in engineering or related scientific subject;
  • A high professional level of Dutch and above average proficiency in English;
  • At least 1 year of experience in Quality Assurance in a GMP environment;
  • Knowledge of the pharmaceutical, medical devices, biotechnology and/or diagnostics industry;
  • A natural mature mindset, extensive communicative skills and able to successfully cope with complexity;
  • Mobility towards the Antwerp province in Belgium.
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Scadenza: 10-01-2026

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