🔍 Cleanroom & Equipment Validation Consultant

📍 Location: Leuven
🕓 Type: Full-time

QbD Group team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD’er in Cleanroom & Equipment Validation.

💡 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

As a Qualification & Validation Specialist, you will be working on-site at one of our pharmaceutical or biotech clients. Your primary responsibility will be to support, execute and coordinate qualification and validation activities related to cleanrooms and critical GMP equipment.

• Drafting and executing qualification protocols (URS, DQ, IQ, OQ, PQ).
• Supporting qualification projects for:
  • Cleanrooms and HVAC systems
  • GMP-critical equipment such as autoclaves, refrigerators, incubators, etc.
  • Utilities (e.g. WFI, compressed air, nitrogen – if applicable)

• Reporting on qualification results and preparing summary reports.
• Managing deviations and implementing CAPAs

💪 What you bring

• You hold a bachelor’s or master’s degree in a scientific or technical field (e.g. Biotechnology, Pharmaceutical Sciences, Industrial Engineering…).
• You have at least 1–2 years of experience in qualification and/or validation in a GMP environment.
• Experience with cleanroom qualification is required.
• Experience with equipment qualification (e.g. autoclaves, fridges, incubators) is a strong plus.You are detail-oriented, analytical, and confident working with GMP documentation.
• You are fluent in Dutch and have a good command of English.

🫵 Who you are

Our culture is driven by values If this sounds like you, you’ll fit right in:

• You’re resilient and tackle challenges with a positive mindset
• You’re curious and always up for learning something new
• You have a no non-sense approach honest, clear, respectful
• You’re innovative and bring ideas, not just opinions
• And above all, you’re serious about your work, but not too serious about yourself

✨ 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.