CQV Engineer - Life Sciences (H/F)

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. As a VIE in Commissioning, Qualification and Validation in the pharmaceutical industry, you will join our expert teams dedicated to ensuring compliance and quality of pharmaceutical facilities and equipment. In this role you will play a key role in • Participating in the development and execution of qualification and validation protocols for pharmaceutical equipment and systems. • Performing commissioning, qualification and validation (CQV) activities in accordance with Good Manufacturing Practices (GMP) and pharmaceutical regulations. • Executing IQ/OQ/PQ testing to verify that systems and equipment are installed correctly, operate as intended, and perform consistently according to specifications. • Collaborating with multidisciplinary teams to ensure facility compliance with regulatory requirements and client specifications. • Documenting test results and writing detailed technical reports. • Identifying deviations and participating in the implementation of corrective actions.