📍 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.
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!
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.
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.
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.
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 usWe 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 Required
- Master's degree in Pharmaceutical Sciences (Industrial Pharmacist) or relevant scientific discipline
- Certified Qualified Person (QP) in accordance with applicable EU regulations
- Proven experience working within GMP-regulated pharmaceutical environments
- Hands-on experience with batch certification and release activities
- Strong knowledge of EU GMP requirements and pharmaceutical quality systems
- Experience handling deviations, CAPAs, change controls, and quality risk assessments
- Experience preparing for and supporting audits, inspections, and health authority interactions
- Experience supporting manufacturing operations, including sterile and aseptic environments
- Fluency in Dutch and English
- Ability to work with cross-functional stakeholders and adapt to various client environments
What We Do
QbD Group is an international life sciences consultancy supporting companies from idea to patient. It provides tailored solutions across development, clinical services, regulatory affairs, quality and compliance, production, distribution, and related software. The company serves advanced therapies, biotech, medical devices, diagnostics, digital health, and pharmaceutical organizations, helping clients accelerate innovation, achieve regulatory compliance, and grow with operational confidence across global markets.
