Analytical Method Transfer Specialist

Job Description:

World leader in engineering and R&D services, Capgemini Engineering combines its broad industry knowledge and cutting-edge technologies in digital and software to support the convergence of the physical and digital worlds. Coupled with the capabilities of the rest of the Group, it helps clients to accelerate their journey towards Intelligent Industry. Capgemini Engineering has 60,000 engineer and scientist team members in over 30 countries across sectors including Aeronautics, Space, Defense, Naval, Automotive, Rail, Infrastructure & Transportation, Energy, Utilities & Chemicals, Life Sciences, Communications, Semiconductor & Electronics, Industrial & Consumer, Software & Internet. 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 Tech Transfer Specialist in the Life Sciences division, you will play a critical role in managing the transfer of manufacturing processes, analytical methods, and technologies from R&D to commercial production or between manufacturing sites. You will work closely with cross-functional teams including R&D, Quality, Regulatory, and Manufacturing to ensure seamless, compliant, and efficient technology transfers. In this position, you will : - Support and coordinate technology transfer projects across internal and external manufacturing sites - Assist in developing and managing tech transfer plans, risk assessments, and gap analyses - Ensure compliance with GMP, regulatory requirements, and internal quality standards - Collaborate with process development, quality assurance, and regulatory affairs teams - Support process validation, scale-up, and troubleshooting activities - Document and report transfer activities, deviations, and resolutions - Contribute to continuous improvement initiatives and digitalization of tech transfer processes

Candidate Requirements:

- Master's degree in Analytical Chemistry, Pharmaceutical Sciences, Biomedical Sciences, Biotechnology, or related field - Recent graduate with 0-2 years of experience - Knowledge of analytical techniques and method validation principles - Understanding of GMP, ICH guidelines, and regulatory expectations for analytical method transfers - Interest in biologics, small molecules, or advanced therapies analytical testing - Ability to work in a fast-paced, matrixed, and multicultural environment - Fluent in English and French or English and Dutch