Quality Assurance Specialist

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.

Youll 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 youll 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 youll 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 were 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 Masters 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 youll fit right in:

• Youre resilient and tackle challenges with a positive mindset

• Youre curious and always up for learning something new

• You have a no non-sense approach honest clear respectful

• Youre innovative and bring ideas not just opinions

• And above all youre serious about your work but not too serious about yourself

Whats 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 wont just be taking a job youll be joining a community where people grow laugh build and contribute to something bigger.

Interested Lets talk.

Send us your CV and motivation letter. You could be the next one to join the QbD family.d be the next one to join the QbD family.