Lab Equipment Qualification Engineer

Job content

???? Qualification & Validation Specialist

???? Location: Hybrid, Belgium

???? Type: Full-time

Are you the kind of person who won’t rest until every system, process, and piece of equipment runs exactly as it should — and can prove it? We’re looking for aQualification & Validation Specialist who’s passionate about quality, precision, and ensuring that life-saving products are backed by rock-solid compliance.

In this role, you’ll play a vital part in guaranteeing that critical equipment and systems meet the highest standards — from installation to performance. If you thrive on structure, enjoy solving technical challenges, and want to make a real impact in the pharmaceutical or life sciences world, then this could be the perfect next step in your career.

???? What’s in it for you

• Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices
• Grow within a community of experts: Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise
• Build a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences
• A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued

???? What you’ll be doing

• Supporting the qualification of lab and production equipment (e.g., installation, operational, and performance qualification activities).
• Reviewing and developing qualification documentation such as risk assessments, protocols, and reports in compliance with regulatory requirements.
• Participating in the design and execution of validation strategiesand ensuring alignment with quality and compliance standards.
• Performing and reviewing test activities (e.g., user acceptance testing) and ensuring proper documentation and traceability.
• Supporting change control, deviation management, and CAPA processes related to equipment qualification.
• Providing training and guidance to end-users on qualification procedures and compliance expectations

???? Who you are

• You have a bachelor or master’s degreein engineering, technological, pharmaceutical or chemical sciences.
• You have a strong interest in or initial experience with equipment qualification, validation, or data integritywithin a GxP-regulated environment.
• You are fluent inthe Dutch or the English language.
• You show a resilient attitude to to tackle any challenge with a positive mindset.
• You are able to communicate effectively and work collaboratively in diverse team environment.
• You show an eye for details and strong technical aptitude.
• You have a genuine passion for contributing to the mission of ensuring quality and compliance in the life sciences industry

✨ About us

We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma.

We believe in JPEG:Joy. Partnership. Going the Extra Mile. Getting Things Done.

You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger!

???? Interested? Let’s talk.

• Send us your CV and motivation letter. You could be the next one to join the QbD family.