Junior Quality Assurance Engineer (Flanders)

About Capgemini

Capgemini is a global leader in partnering with companies to transform and manage their business by harnessing the power of technology. The Group is guided everyday by its purpose of unleashing human energy through technology for an inclusive and sustainable future. It is a responsible and diverse organization of 270,000 team members in nearly 50 countries. With its strong 50 year heritage and deep industry expertise, Capgemini is trusted by its clients to address the entire breadth of their business needs, from strategy and design to operations, fueled by the fast evolving and innovative world of cloud, data, AI, connectivity, software, digital engineering and platforms. The Group reported in 2020 global revenues of €16 billion.
Get the Future You Want | www.capgemini.com

Our offer

We currently offer a specific job in our Life Sciences division with a lot of variation and room for initiative and development. This project gives you the opportunity to come into contact with many different domains within Quality Assurance, etc. We ensure that this project builds on the experience you have already gained and brings you into contact with new inspiring topics. If you recognize a possible next step in your career in this project, we would like to discover with you how closely your profile matches the desired one. Through this project, we launch your Capgemini Engineering career and 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 have the opportunity to provide support with handling complaints, change controls, deviations, CAPA, etc,..
  • You will ensure compliance with standards (FDA, EMA, ICH, ISO…)
  • You are responsible for the QA Qualification of equipment, facilities and utilities
  • You provide Product Quality Reviews (PQR) and the Continued Process Verifications (CPV)
  • You are responsible for operational QA follow-up during the production or distribution of the goods
  • You will have the opportunity to take care of the planning and execution of internal audits
  • You are the trainer for all GMP related topics within the department of the client

Your profile

  • A Master in Pharmaceutical or Biomedical Sciences, Bio-engineering, Chemistry or related scientific fields
  • A very good level of Dutch and fluent in English
  • Not necessary, but a first experience in Quality Assurance in a GMP environment
  • A natural drive, communication skills and strong motivation
  • Knowledge of or a strong interest in the Pharmaceutical Industry, Medical Devices, Biotechnology or Diagnostics



Posted on:

June 2, 2021

Experience level:

Entry level

Contract type: