At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as they provide unique R&D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days are the same.
À propos du poste
Intégrez le département Qualité pour contribuer au traitement des CAPA et des déviations dans le respect des normes GMP et des exigences réglementaires de l’industrie pharmaceutique. Vous participerez à la mise en œuvre des actions correctives et préventives afin de garantir la conformité et l’amélioration continue des processus qualité.
Lieu : Casablanca
Durée : CDI
Expérience : 0 à 3 ans dans l’industrie pharmaceutiqueLangues : Bon niveau en français et en anglais
Les missions du poste
Votre profil
Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fueled by its market leading capabilities in AI, generative AI, cloud and data, combined with its deep industry expertise and partner ecosystem.
