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Capgemini Engineering is seeking an experienced Commissioning, Qualification and Validation Engineer for the pharmaceutical industry in Diegem, Belgium. You will join expert teams to ensure compliance and quality of pharmaceutical facilities and equipment.
You will develop and execute qualification/validation protocols, perform CQV activities in line with GMP, and document results with detailed reports. You will collaborate across disciplines and contribute to corrective actions as deviations
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 mostinnovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as theyprovide 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 arethe same.
As a Commissioning, Qualification and Validation Engineer in the pharmaceutical industry, you will join our expert teams dedicated to ensuring compliance and quality of pharmaceutical facilities and equipment.
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.