Job Description

🔍Qualified Person (QP)

📍 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!

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. 

💪 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.