Overview
Quality Management Specialist Jobs in Flemish Region, Belgium at QbD Group
Title: Quality Management Specialist
Company: QbD Group
Location: Flemish Region, Belgium
🔍 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 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 th
