Validation & Qualification Engineer - Barcelona at QbD Group

Rubí, Catalonia, Spain -

Full Time

Start Date

Immediate

Expiry Date

13 Jan, 26

Salary

0.0

Posted On

15 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Validation, Qualification, GMP, Engineering, Pharmaceutical Sciences, Chemical Sciences, Spanish, English, Collaboration, Attention To Detail, Technical Aptitude, Compliance, Risk Assessment, Auditing, Continuous Learning, Innovation

Industry

Business Consulting and Services

Description

🔍 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.

Responsibilities

The Validation & Qualification Engineer will collaborate in executing and drafting automation protocols, ensuring compliance of equipment and processes. They will also support internal and external audits and contribute to validation plans and reports.