Qualified Person (QP)

QbD Group; Vlaanderen; Sur place; EUR 70 000 - 100 000; Plein temps

Résumé du poste

QbD Group in Belgium is seeking an experienced Qualified Person to support GMP-regulated product release and quality oversight across life sciences clients.

You will review deviations, lead batch certification activities, and collaborate with cross-functional teams including Regulatory Affairs, QC and Production to ensure patient safety and compliance.

Qualifications

• Master's degree in Pharmaceutical Sciences or equivalent.
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Responsabilités

• Perform batch certification and release support.
• Review deviations, CAPAs, change controls, and quality risk assessments.
• Support audits, inspections, and health authority interactions.
• Collaborate with Production, QC, QA, Engineering, and Regulatory Affairs.

Connaissances

GMP knowledge

Quality systems

Stakeholder management

Deviations handling

Formation

Master's degree in Pharmaceutical Sciences

Outils

CAPA management

Change controls

Regulatory inspections

Description du poste

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.

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.

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.