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Validation & Qualification Engineer

Trabajo disponible en: 08001, Barcelona, Cataluna, España
Empresa: TRIUM Clinical Consulting NV
Tiempo completo posición
Publicado en 2026-01-20
Especializaciones laborales:
  • Ingeniería
    Ingeniería de Calidad, Ingeniero de Procesos, Ingeniero biomédico
Rango Salarial o Referencia de la Industria: 50000 - 70000 EUR Anual EUR 50000.00 70000.00 YEAR
Descripción del trabajo

🔍 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 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.

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