🔍Qualified Person (QP)
đź“Ť Location: Hybrid
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.
🚀 Put Your QP Expertise to Work
Are you a certified Qualified Person (QP) looking for challenging projects in the pharmaceutical and biotech industry? At QbD Group, you'll apply your expertise across a variety of GMP-regulated environments, supporting leading life sciences companies with quality, compliance, and batch certification activities.
Whether you prefer working with a dedicated client or across multiple projects, you'll benefit from a strong network of experts, continuous knowledge sharing and the variety of consultancy combined with the stability of one employer!
What you'll be doing
You'll play a key role in ensuring product quality, patient safety and GMP compliance. Depending on the project and client, your responsibilities may include:
- Performing batch certification and supporting batch release activities.
- Providing GMP oversight and ensuring compliance with EU GMP requirements.
- Reviewing and approving deviations, CAPAs, change controls, and quality risk assessments.
- Supporting manufacturing operations, including sterile and aseptic environments.
- Preparing for and supporting audits, inspections, and interactions with health authorities.
- Acting as a trusted quality partner for cross-functional stakeholders across Production, QC, QA, Engineering, and Regulatory Affairs.
- Driving continuous improvement initiatives within quality systems and compliance processes.
đź’Ş What you bring
We're looking for experienced quality professionals who are ready to make an impact within GMP-regulated environments and support our pharmaceutical clients as a Qualified Person.
You might be the perfect fit if you:
- Hold a Master's degree in Pharmaceutical Sciences (Industrial Pharmacist) or another relevant scientific discipline.
- Are a certified Qualified Person (QP) in accordance with applicable EU regulations.
- Have proven experience working within GMP-regulated pharmaceutical environments.
- Have hands-on experience with batch certification and release activities.
- Possess strong knowledge of EU GMP requirements and pharmaceutical quality systems.
- Have experience with deviations, CAPAs, change controls, audits and regulatory inspections.
- Are comfortable working with different stakeholders and adapting to various client environments.
- Are fluent in Dutch and 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.
- 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.
