Equipment Qualification Engineer

QbD Group; Vlaanderen; Sur place; EUR 55 000 - 70 000; Plein temps

Résumé du poste

QbD Group in Belgium is seeking (experienced) Qualification Engineers who are passionate about quality, precision and ensuring life-saving products are backed by robust compliance. You will oversee qualifications from installation to performance, contributing to stability and regulatory alignment within the life sciences sector.

Join a team of experts dedicated to training, documentation, and continuous improvement, with a clear path to growing your expertise in GMP, validation strategies, risk

Qualifications

• Bachelor's or Master's degree in engineering, technological, pharmaceutical or chemical sciences.
• Experience with equipment qualification, validation, or data integrity in a GxP-regulated environment.
• Fluent in Dutch or English; strong communication and teamwork skills.

Responsabilités

• Supporting the qualification of lab and production equipment (installation, operational, and performance qualification).
• 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 strategies and ensuring alignment with quality and compliance standards.
• Performing and reviewing test activities 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.

Connaissances

Equipment qualification

Validation

Data integrity

GxP compliance

Quality assurance

Formation

Bachelor's or Master's degree in engineering or related sciences

Description du poste

Are you the kind of person who won’t rest until every system, process, and piece of equipment runs exactly as it should? We’re looking for (experienced) Qualification Engineers who are 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.
• 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 strategies and 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 degree in engineering, technological, pharmaceutical or chemical sciences.
• You have a strong interest in or proven experience with equipment qualification, validation, or data integrity within a GxP-regulated environment.
• You are fluent in the 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

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!