Equipment Qualification Engineer | Life Sciences

Your Role

In this role, you will play a key role in supporting our client's Equipment Requalification program at their Geel site in Belgium, working as part of a broader global Quality Transformation initiative. You will work autonomously on-site, collaborating closely with Engineering, Quality, Manufacturing, and Validation teams to deliver high-quality GMP documentation and ensure full compliance with regulatory standards.

In this role you will play a key role in:

• Supporting equipment qualification and requalification activities within a GMP-regulated pharmaceutical manufacturing environment, ensuring all activities are executed to the highest quality and compliance standards
• Preparing, executing, and reviewing IQ / OQ / PQ documentation in line with GMP / GxP requirements, contributing to the overall success of the Equipment Requalification workstream
• Contributing to Commissioning, Qualification, and Validation (CQV) activities, including the assessment and requalification of utilities, facilities, and process equipment
• Managing and contributing to deviation identification, CAPA follow-up, and remediation plans related to equipment qualification gaps, ensuring timely and compliant resolution
• Supporting inspection readiness activities when required, ensuring documentation and processes are audit-ready at all times

Your Profile

We are looking for an experienced Qualification / Validation professional who is confident working autonomously in a fast-paced, regulated pharmaceutical environment. You will bring strong technical knowledge, a rigorous approach to documentation, and the ability to collaborate effectively with cross-functional site teams.

• Minimum 3 years of experience in equipment qualification, validation, or a related role within a pharmaceutical or biopharmaceutical manufacturing environment
• Hands-on experience with IQ / OQ / PQ protocols, CQV methodologies, and GMP / GxP documentation standards, with the ability to both prepare and critically review qualification documentation
• Demonstrated experience working with utilities, facilities, and process equipment in a regulated manufacturing setting, including involvement in commissioning and qualification activities
• Strong understanding of deviation management and CAPA processes, with the ability to contribute to remediation plans and support cross-functional teams in resolving qualification gaps
• Fluency in English and Dutch for effective communication with local site teams in Geel

What You Will Love About Working Here

• Impact Together Week – During this week, we volunteer for activities supporting a sustainable and inclusive future. Over 7,000 volunteers have contributed skills and time to help those in need.
• 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 learning platforms – Free access for all to world-class learning assets and curated programs from Harvard Business Review, Coursera, Pluralsight, Udemy, Microsoft, AWS, Google and many more.