Validation & Qualification Engineer (SCADA experience)

Job Summary

Join QbD Group as a Validation & Qualification Engineer (SCADA experience).

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.

What you’ll be doing

• Collaborate in the execution and drafting of automation protocols (room integration, reading electrical panels and drawings, SCADA execution, etc.) depending on your preference and expertise.
• Monitor and ensure that equipment, utilities, qualified areas and processes are compliant.
• Develop and implement validation strategies following internal procedures and industry regulations.
• Contribute to the drafting of validation plans, protocols, risk assessments and reports under the guidance of experienced consultants.
• Provide support during internal and external audits, gaining valuable exposure to industry best practices.
• 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.
• Experience in qualification & validation within the life sciences industry is preferred, but fresh talent eager to learn is welcomed.
• You are fluent in Spanish and English (B2).
• You show a resilient attitude, tackling challenges with a positive mindset.
• You can communicate effectively and work collaboratively in a diverse team environment.
• You have an eye for detail 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

• Resilient and tackling challenges with a positive mindset.
• Curious and always up for learning something new.
• Have a no-nonsense, honest, clear, respectful approach.
• Innovative and bring ideas, not just opinions.
• Serious about your work, but not too serious about yourself.

Job details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Engineering, Science, and Writing/Editing
• Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Engineering Services
• Location: Sant Just Desvern, Catalonia, Spain

How to apply

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

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