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!
You will support change control and its implementation,
You will participate in handling customer complaints,
You will investigate deviations and non-conformities in cross-functional teams,
You will initiate and assure following up on CAPA (Corrective Action Preventive Action)
You will review batch records in accordance with release requirements
You will review validation documentation (Production, Quality Control…)
You will help write and assess APR (Annual Product Review) and QPR (Quality Performance Review).
You will ensure compliance with standards (FDA, EMA, ICH, ISO…)
Master degree in engineering or related scientific domains
Native level of French or Dutch and fluent in English
At least 3 years' experience in Quality Assurance in a GMP environment
Knowledge of Pharmaceutical Industry, Medical Devices, Biotchnology or Food technology
Discover more about your career on www.altran.be/careers