🔍 Validation & Qualification Engineer

📍 Location: Barcelona
🕓 Type: Full-time

Are you someone who thrives in regulated environments (GMP) and enjoys making a real impact by ensuring everything runs safely, smoothly, and compliantly? Then you might be the Validation & Qualification Engineer we’re looking for!

💡 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.

🏢 What you’ll be doing

• Depending on your preference/expertise, you collaborate in the execution and drafting of automation protocols (room integration, reading electrical panels and drawings, SCADA execution, etc.).
• You monitor and ensure that equipment, utilities, qualified areas and processes are compliant.
• You learn to develop and implement validation strategies following internal procedures and industry regulations.
• You contribute to the drafting of validation plans, protocols, risk assessments and reports under the guidance of experienced consultants.
• You provide support during internal and external audits, gaining valuable exposure to industry best practices.
• You uphold a culture of knowledge sharing and continuous learning within the QbD Group.

💪 What you bring

• You have a master’s degree in engineering, technological, pharmaceutical or chemical sciences.
• While experience in qualification & validation within the life sciences industry is preferred, we welcome fresh talent eager to learn.
• You are fluent in Spanish and English (B2) language.
• You show a resilient attitude to to tackle any challenge with a positive mindset.
• You are able to communicate effectively and work collaboratively in diverse team environment.
• You show an eye for details and strong technical aptitude.
• You have a genuine passion for contributing to the mission of ensuring quality and compliance in the life sciences industry!

🫵 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

✨ About us

We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 600+ 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.