🔍 Quality Management Specialist At QbD Group, we support the life sciences industry — pharma, biotech, medical devices, and digital health — across the entire product life cycle. You’ll join an award-winning, fast-growing international team of 650+ experts, where knowledge sharing, innovation, and people truly come first. We are a knowledge-based company where continuous learning and meaningful impact are at the heart of everything we do. We are looking for our next QbD’er in Quality Assurance! 🏢 What you’ll be doing As a Quality Management Specialist, you play a key role in ensuring robust and compliant Quality Management Systems within GMP-regulated environments. You will work closely with QA teams and cross-functional stakeholders in dynamic and innovative settings. Depending on the project setup and your preferences, you may work in a consulting model with multiple clients or be assigned to a mid/long-term engagement with a single client , allowing you to either broaden your experience across different environments or deepen your impact within one organization. Your responsibilities include: Providing expert advice and hands-on support on Quality Management Systems (QMS). Managing and supporting CAPAs, deviations, change controls, complaints, and quality events. Performing QA batch record review and supporting material and batch release processes. Ensuring compliance with applicable GMP guidelines and regulatory requirements. Collaborating with internal and external stakeholders to drive continuous quality improvements. Contributing to audits, inspection readiness and quality system optimization. 🎯 Who we are looking for You hold a Bachelor or Master’s degree in Pharmacy, Bioengineering, Biomedical Sciences, Applied Sciences, or a related scientific field. You have at least 3 years of experience in QA within a GMP-regulated environment, preferably in commercial manufacturing. You have a strong understanding of GMP, Quality Systems and regulatory compliance. You have a structured, detail-oriented mindset with a strong focus on product quality. You are flexible, stress-resistant, and comfortable working in dynamic environments. 🫵 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. You take ownership and enjoy solving complex challenges. And above all, you’re serious about your work, but not too serious about yourself. 💡 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. ✨ 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.
Quality Management Specialist • Région Wallonne, Belgium
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