Quality Assurance Consultant

🔍 Quality Assurance Consultant

📍 Location: Barcelona - On-site

🕓 Type: Full-time

 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.

As a Quality Assurance Consultant you’ll get the unique opportunity to:

• Build a broad quality skillset across different environments

• Work on diverse projects at multiple or one dedicated client

All while being supported by experienced mentors and working for one stable employer: QbD Group.

🏢 What you’ll be doing

As a Quality Consultant, you will gain hands-on experience across different projects and companies, allowing you to quickly develop both your technical expertise and professional skills.

• Build hands-on GMP experience: Support batch review and release, interpret GMP documentation, and learn the QP role within EU GMP.

• Expand your quality systems knowledge: Work on deviations, CAPAs, and change controls while contributing to improvements and gaining exposure to sterile manufacturing.

• Experience diverse environments: Join projects across pharmaceutical/MedTech/Biotech companies and build a versatile industry profile.

• Grow into a quality professional: Develop stakeholder communication, problem-solving, and take on increasing responsibility.

• Get exposure to audits & inspections: Support inspections and learn how to prepare documentation and interact with authorities. 

💪 What you bring

Already have experience in GMP and ready to take the next step in your professional career At QbD, we’re looking for motivated professionals who want to grow fast by working on diverse projects across different clients and environments.

You might be the perfect fit if you:

• Hold a Master’s degree in Pharmaceutical Sciences (Industrial Pharmacist) or another relevant scientific field.

• Have hands-on experience with GMP .

• Are eager to deepen your expertise in sterile manufacturing and regulatory compliance.

• Are fluent in Spanish 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

• 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.