Validation and Compliance Project Engineer | Life Sciences
Job in
Town of Belgium, Belgium, Ozaukee County, Wisconsin, 53004, USA
Listed on 2026-07-17
Listing for:
Capgemini
Full Time
position Listed on 2026-07-17
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist -
Engineering
Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below
# Validation and Compliance Project Engineer | Life Sciences Diegem Apply for this job
* Permanent* Experienced Professionals
* Quality Engineering & Testing
* -en GBAt 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 We are looking for a Medior Project Engineer - Validation & Compliance to join our team in Flanders, Belgium. In this role, you will coordinate validation and verification activities within capital projects in a regulated pharmaceutical environment, acting as a key interface between Engineering and Quality Assurance to ensure safe, compliant, and efficient project delivery.
In this role you will play a key role in:* +
** Coordinating validation and verification activities
** across capital projects, developing and monitoring project schedules from planning through to full implementation, ensuring all milestones are met with accuracy and compliance at the forefront +
** Interpreting and applying GMP regulations** (US and EU), international standards (ISO, ICH), and internal quality standards, serving as the primary liaison between Engineering and Quality Assurance teams to maintain alignment throughout project life cycles +
** Drafting, reviewing, and managing
** validation protocols, qualification documentation, and technical compliance documents, upholding the highest standards of technical writing and documentation accuracy at all times +
** Facilitating Quality Risk Assessments (QRM)
** and providing expertise in validation, verification, and risk management, as well as supporting investigations related to quality issues, deviations, and change control processes +
** Managing one or more projects simultaneously**, contributing to continuous improvement initiatives, supporting the introduction of new products, and addressing urgent quality investigations with a structured and solution-driven approach +
** Supporting qualification and validation of analytical methods
** and contributing to the development of computer-controlled systems where applicable, while also providing backup support to fellow project engineers as needed## Your Profile
* You hold a
** Master's degree
** in Engineering (Civil, Industrial, or Bio-engineering), Industrial Pharmacy, or a relevant scientific field such as Biochemistry, Biotechnology, or a related discipline — equivalent experience will also be considered
* You bring a minimum of
** 2 years of experience
** in a regulated pharmaceutical or production environment, with a solid understanding of GMP requirements and validation and qualification processes
* You demonstrate
** strong communication and stakeholder management skills**, with the ability to collaborate effectively across cross-functional teams, manage multiple priorities in a dynamic environment, and take ownership of your responsibilities with attention to detail and reliability
* You are
** fluent in both Dutch and English**, with excellent technical writing capabilities and a structured, detail-oriented working style that ensures accuracy and quality in every deliverable
* Experience with
** aseptic processes, cleaning, disinfection, sterilisation**, or laboratory environments is a strong advantage and will be highly valued## What You Will Love About Working Here
* ** Hybrid working** – We encourage flexibility when it comes to when and where work gets done. Employees work with their managers to determine an arrangement that works best for their role and personal circumstances.
* ** Mentoring programs** – Capgemini empowers women at all career stages with programs spanning STEM education to career reentry. We value mentorship for fostering professional growth and empowerment within our engineering community.
* ** Free access to…
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