QA Consultant

QbD Group | Spain; Barcelona; On-site; EUR 42,000 - 60,000; Full time

Job summary

QbD Group is seeking a Quality Assurance Consultant to support GMP activities across pharma, biotech, medical devices, and digital health. You will join a fast-growing, international team of 650+ experts, gaining hands-on experience in GMP batch review, deviation handling, and regulatory compliance.

The role offers exposure to audits, multiple client projects, and a path to grow as a quality professional within a stable employer. Fluency in Spanish and English is required.

Qualifications

• 1–7 years of GMP experience required.
• Master’s degree in Pharmaceutical Sciences or related field.
• Fluent in Spanish and English.

Responsibilities

• Gain hands-on GMP experience: support batch review, release, and learn GMP documentation.
• Expand quality systems knowledge: work on deviations, CAPAs, and change controls.
• Experience diverse environments across pharma/biotech/MedTech projects.
• Develop stakeholder communication and problem-solving skills.
• Assist with audits and inspections: prepare documentation and interact with authorities.

Skills

GMP experience

Quality assurance

Stakeholder communication

Problem solving

Education

Master’s in Pharmaceutical Sciences

Job description

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 1 to 7 years 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.

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.