Senior CSV Consultant to Capgemini Engineering Malmö

Are you passionate about and experienced in Computerized System Validation?
Join us and get the future you want!
Capgemini Engineering is in a global leading position within innovation, development and engineering. Together with our partners we are facing exciting challenges whilst creating the future. Our team is taking the efficiency, quality and compliance of our partners to the next level in order to develop smarter products and become an even stronger player within the life science industry.
Our offer
By offering exciting opportunities of career development you can get the future you want.
Capgemini Engineering offers you a work environment that is characterized by innovation. As a consultant at Capgemini Engineering, you are part of something bigger. We deliver, together with our global centers of expertise, solutions for both large global customers and smaller local start-ups. We are driven by meeting the customer's needs and generating added value. In the Life Science Team in Malmö, we work with both medical device and pharm clients.
Your Role
As a consultant in our life science team, you will be leading quality management in development projects related to computerized System Validation. In many of our client assignments, our consultants work in teams provided to the client by Capgemini Engineering – but in close collaboration with employees of the client. You may be working in accordance with clients processes as well as with applicable standards and legislations in order to ensure quality assured activities and documentation throughout the process.
You as an individual are self-driven, prestige-less and a team-player. We expect that you will lead others and that you are interested in taking the driver’s seat with regard to your own development as well as your colleagues. You find the consultant role interesting and thrive in a varied environment where changes sometimes take place with abrupt changes.
Your profile
You have:
A degree in engineering, a master of science, data/IT science degree or similar,
Long experience within GxP computer validation in Pharmaceutical and Medical Device Industries.
Knowledge of and/or experience of working accordance with regulations, guidelines and standards such as: GAMP5, EU GMP, US GMP, 21 CFR Part 11, ISO 13485, ISO 27001 etc
The ability to communicate fluently in spoken and written English.



You as a person are:
Curious and motivated by exciting challenges,
A person who takes initiatives, is flexible and thrives in a dynamic environment,
A person who finds it easy to cooperate and communicate with different groups of people,
Genuinely interested in technology and problem solving, and driven by challenges and personal development.



About Us
Capgemini Engineering is one of the world’s leading consultant companies within R&D. We are part of Capgemini Group with around 270 000 employees globally. In Scandinavia, our main areas of business are Industry, Automotive, Life Science and the Public Sector. Together with our global centers of expertise, we deliver solutions to both global clients and local start-up companies.
Based on the need of the client, we provide competence, complete project teams and services. We always adapt our solutions and services to the client’s organization and challenges.
Our organization is characterized by a team spirit atmosphere and leaders whose main focus is to support the consultants in their projects. We actively work to promote participation by regularly organize team breakfasts and lunches, after works, sport events and other fun activities!
We care about our employees, and to us it is important that all our employees have a close connection to their teams as well as team managers.
Application and Contact
Interviews are ongoing.
If you have questions or want more information, please contact our Talent Acquisition Partner Martin Svensson at martin.svensson@capgemini.com
We kindly refrain from contact with advertises and employment agencies in the recruitment process.