Validation & Qualification Engineer (SCADA experience)

QbD Group; Barcelona; Presencial; EUR 40.000 - 60.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Knowledge-sharing and mentoring

Competitive compensation package

Growth opportunities in a community of experts

Descripción de la vacante

A life sciences consulting firm is looking for a Validation & Qualification Engineer to join their team in Spain. This role involves collaborating on protocols, ensuring compliance, and developing validation strategies. Candidates should have a master's degree in a related field and fluency in Spanish and English. The firm is focused on creating a positive impact in the life sciences industry and supports continuous learning and growth for its employees. The position offers a full-time opportunity in a vibrant and innovative environment.

Formación

• Experience in qualification & validation within the life sciences industry is preferred.
• Fresh talent eager to learn is welcomed.
• Curious and always willing to learn.

Responsabilidades

• Collaborate in execution and drafting of automation protocols.
• Monitor compliance of equipment and processes.
• Develop validation strategies per internal procedures.
• Draft validation plans and protocols.
• Support during audits.

Conocimientos

Fluent in Spanish

Fluent in English (B2)

Attention to detail

Strong technical aptitude

Collaborative teamwork

Educación

Master’s degree in engineering, technological, pharmaceutical or chemical sciences

Descripción del empleo

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.