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# https://schema.org

- **Company:** Kymos
- **Location:** Barcelona, Spain
- **Contract:** Permanent contract
- **Skills:** Data Integrity, Supervisory Control and Data Acquisition (SCADA), Laboratory Information Management Systems, Test Execution Engine, GXP
- **Published:** August 16, 2026
- **Apply:** https://es.trabajo.org/oferta-4021-bdbbfe4db26e848ef2ab8cd4a073af7c

## About the Role

in regulated GMP and GLP environments. Our laboratories are equipped with a wide range of analytical instruments and computerized systems, including solutions such as LIMS, Empower, laboratory software, and other corporate systems. We are currently looking for someone to join our Computer System Validation - CSV area, based in Cerdanyola del Vallès, Barcelona. We are looking for a profile with some previous experience or knowledge in CSV, quality, laboratory environments, or computerized systems, who is willing to continue developing in a regulated and highly technical environment. Main objective To support the validation, maintenance, and review activities of computerized systems used in the laboratory and in other company processes, ensuring compliance with applicable regulatory requirements in GxP environments. Main responsibilities - Participate in computer system validation activities, both for laboratory equipment and other systems. - Support the, normativas o guías como GAMP 5, EU GMP Annex 11, 21 CFR Part 11, ISO o GxP. - Conocimientos o experiencia con sistemas como LIMS, Empower, SCADA, ERP u otros softwares de laboratorio o corporativos. - Capacidad para trabajar en equipo con departamentos técnicos, laboratorio, IT y Garantía de Calidad. - Buen nivel de organización, atención al detalle y orientación al cumplimiento. - Nivel avanzado de español e inglés, hablado y escrito. Si te unes a nosotros, podrás disfrutar: - Incorporación a una compañía especializada y en crecimiento. - Desarrollo profesional en un área técnica con alta demanda en el sector farmacéutico. - Acompañamiento por parte de equipos expertos en calidad, laboratorio, IT y sistemas. - Entorno colaborativo y dinámico. - Horario flexible e intensivo los viernes. - Modelo híbrido, con presencia principalmente en oficina. - Plataforma de beneficios para empleados. - 23 días de vacaciones

## Description

aplicables en entornos GxP. Principales funciones - Participar en actividades de validación de sistemas informatizados, tanto de equipos de laboratorio como de otros sistemas. - Dar soporte en la elaboración y revisión de documentación de validación, como Validation Plan, Risk Analysis, Design Review, IOPQ, Traceability Matrix y Final Validation Report. - Colaborar en la evaluación de requisitos de integridad de datos, cumplimiento regulatorio y control de cambios. - Apoyar en la preparación y ejecución de pruebas, planes de test y pruebas de aceptación de usuario. - Participar en revisiones periódicas de sistemas informatizados. - Colaborar con los equipos de Quality Assurance, IT, LIMS y Laboratorio en proyectos relacionados con sistemas informatizados. - Dar soporte en auditorías internas y en la preparación de documentación relacionada con CSV. At Kymos Group, we provide specialized analytical services to the pharmaceutical industry


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