Quality Management Specialist

🔍 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 Bachelor or 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 the QbD family.