Portugal
NOS
Capgemini
CQV Engineer
Portugal
Fundão, Portugal · Lisbon, Portugal · Vila Nova de Gaia, Portugal
About the opportunity
CQV ENGINEER
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.
YOUR ROLE
- Support commissioning and qualification activities within regulated environments, ensuring compliance with internal procedures, SOPs, and project requirements.
- Draft, author, review, execute, and maintain commissioning and qualification lifecycle documentation using Kneat and other quality systems.
- Prepare and maintain commissioning and qualification protocols, test cases, and strategic documentation, including system classification documents.
- Execute validation protocols, including prerequisites, testing, and evidence documentation within electronic systems.
- Participate in FAT and SAT activities, including remote support when required.
- Support deviation management, test incident resolution, and follow-up actions.
- Contribute to change control activities and ongoing documentation updates throughout the project lifecycle.
- Collaborate with multidisciplinary teams across Capgemini Engineering and participate in regular follow-up meetings, reporting progress and maintaining updated project trackers.
YOUR PROFILE
- We are seeking a CQV Engineer to join our team in the Life Sciences sector.
- This position is especially suitable for professionals with at least 3 years of
- experience in commissioning and qualification (CQV or C&Q) within regulated
- industries, who are looking to grow in an international and multidisciplinary
- environment.
- Candidates should have experience working with electronic validation or
- qualification systems and demonstrate strong technical documentation skills,
- attention to detail, and the ability to collaborate effectively across teams
- while managing execution activities, incidents, and documentation updates.
- This role is suitable for candidates with an academic background in Pharmacy,
- Biomedicine, Biomedical Sciences, or Bioengineering. We value curiosity,
- willingness to learn, and motivation to grow within the Life Sciences field.
- WHAT YOU’LL LOVE ABOUT WORKING HERE
- Join a multicultural and inclusive team environment.
- Enjoy a supportive atmosphere promoting work life balance.
- Hybrid work.
- Your career growth is central to our mission. Our array of career growth
- programs and diverse professionals are crafted to support you in exploring a
- world of opportunities.
- Access valuable training and certifications in cutting edge technologies.
- Engage in exciting projects.
- Health and life insurance.
- Referral program with bonuses for talent recommendations.
- Great office locations.
- ABOUT CAPGEMINI
- Capgemini is an AI-powered global business and technology transformation
- partner, delivering tangible business value. We imagine the future of
- organizations and make it real with AI, technology, and people. With our strong
- heritage of nearly 60 years, we are a responsible and diverse group of 420,000
- team members in more than 50 countries. We deliver end-to-end services and
- solutions with our deep industry expertise and strong partner ecosystem,
- leveraging our capabilities across strategy, technology, design, engineering and
- business operations.
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