Descripción de la oferta
Job SummaryJoin QbD Group as a Validation & Qualification Engineer (SCADA experience).What’s in it for youMake 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 doingCollaborate 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 bringYou 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 areResilient 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 detailsSeniority level: Mid-Senior levelEmployment type: Full-timeJob function: Engineering, Science, and Writing/EditingIndustries: Pharmaceutical Manufacturing, Biotechnology Research, and Engineering ServicesLocation: Sant Just Desvern, Catalonia, SpainHow to applySend us your CV and motivation letter. You could be the next one to join the QbD family.
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