
Open since Jul 2026
Sterility Process Engineering Expert
AI Summary
Supports clients in achieving compliance with updated sterile manufacturing requirements by providing hands-on expertise in isolators, RABS, cleanroom qualification, and contamination control strategies.
About this role
📍 Location: Flanders
đź•“ Type: Full-time
🏢 What you’ll be doing
Join our new Annex 1 solution experts and support clients in achieving compliance with updated sterile manufacturing requirements. You'll bring hands-on expertise in isolators, RABS, cleanroom qualification, and contamination control.
💡 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.
đź’Ş What you bring
Senior experience in sterile manufacturing environments
Proven isolator/RABS qualification experience
Knowledge of cleanroom design and qualification
Expertise in aseptic techniques and process validation
Deep understanding of contamination control strategies (CSS plan) and Annex 1 requirements
Experience with environmental monitoring (EM) programs
🫵 Who you are
You're a sterile manufacturing specialist who understands the critical nature of this work
You combine technical rigor with practical problem-solving
You stay current with regulatory changes (Annex 1, PIC/S)
You're quality-focused and comfortable working in high-stakes environments
✨ 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.
Skills
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