Validation Engineer | Life Sciences
Confirmed on the employer's own hiring board on Oct 6, 2026. First seen by Alion on Jun 16, 2026. Capgemini scores B on the Alion truth index.
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
As a Validation Engineer, you will play a crucial role in ensuring pharmaceutical manufacturing processes, equipment, and cleaning procedures meet regulatory requirements and quality standards. Working with cross-functional teams, you'll help our clients maintain compliance while optimizing their validation processes.
In this role you will play a key role in:
- Executing validation protocols including IQ/OQ/PQ for equipment and process validation batches
- Developing and reviewing cleaning validation documentation, performing risk assessments and worst-case analyses
- Preparing validation master plans, protocols, and comprehensive validation reports
- Collaborating with engineering, production, and quality teams to ensure validation activities align with GMP requirements
- Supporting regulatory inspections and audits by providing validation documentation and expertise
- Leading investigations related to deviations and implementing CAPA (Corrective and Preventive Actions)
- Maintaining validation lifecycle documentation and performing impact assessments for changes
Your Profile
- Bachelor's or Master's degree in Engineering, Pharmaceutical Sciences, Chemistry, or related technical field
- Fluency in Dutch and English
- 2-5 years of experience in validation within the pharmaceutical or life sciences industry
- Hands-on experience with equipment qualification (IQ/OQ/PQ), cleaning validation, and/or process validation
- Strong knowledge of GMP regulations, FDA/EMA requirements, and industry validation standards
- Experience with risk assessment methodologies and contamination control strategies
- Excellent analytical skills with ability to interpret validation data and prepare technical reports
- Strong communication and collaboration skills to work effectively in cross-functional teams
What You'll Love About Working Here
- Continuous feedback: We take human-centric approach to foster growth and performance. Our performance management tool GetSuccess enables continuous feedback, quarterly check-ins with managers, and ongoing performance discussions.
- FlexAbroad: Employees in 20+ countries can work abroad for up to 45 days in a 12-month period.
- Digital campuses and academy: Our engineering academy offers more than 60,000 hours of training, as also our digital campus on GenAI, data or sustainability, support digital learning in the flow of work from awareness to expert certifications.
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.