IVD Validation Specialist

Tipo de Contrato: Indefinido tiempo completo Número de solicitud de puesto: 547258 ¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de...

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. Due to a constant growth, we are looking for a Computer System Validation...

Are you the kind of person who won’t rest until every system, process, and piece of equipment runs exactly as it should — and can prove it? We’re looking for a Qualification & Validation Specialist who’s passionate about quality, precision, and ensuring that life-saving products are backed by rock-solid compliance. In this role, you’ll play a vital...

Desde Talent Search People, en colaboración con una importante multinacional farmacéutica, nos encontramos en búsqueda de un/a Technical Service Specialist para realizar mantenimiento de dispositivos médicos especializados en el diagnostico clínico de hematología, urianalisis e inmunología, entre otras especialidades en Murcia. ¿Qué harás?...

Werfen is seeking an Enterprise Systems Digital Assurance Specialist to support Corporate QA IT. The role focuses on validating and ensuring audit readiness for cloud/Kubernetes platforms, external data center services, and integrations, while aligning with IT governance and documentation standards. You will collaborate with IT teams, business stakeholders...

Grifols, S.A busca un/a Técnico/a de Validaciones de equipos y procesos para gestionar y ejecutar proyectos de validación conforme a la normativa vigente, asegurando la validez de los procesos productivos. La posición exige Grado en Ingeniería, experiencia de 1 a 3 años, inglés avanzado (B2.2), dominio de Office y SAP, y disponibilidad para viajar; se...

KYMOS GROUP, a growing CRO with HQ in Spain, seeks a Computer System Validation professional for the Barcelona area. You will support validation of laboratory and other computerized systems in regulated GxP environments, ensuring regulatory compliance and data integrity. You will collaborate with QA, IT and Laboratory teams, handling validation plans, risk...

A leading life sciences company in Barcelona is seeking a Qualification and Validation Specialist to ensure quality in validation processes within the pharmaceutical and medical device industries. Responsibilities include conducting validation and qualification of equipment and processes, managing documentation, and supporting compliance efforts. Candidates...

Mira seeks a Regulatory Submission Specialist to lead regulatory documentation for IVD devices. You will ensure clinical, analytical, usability, risk-management, quality, and labeling evidence is compiled into submission-ready materials and supports compliance across the product lifecycle. The ideal candidate has experience in regulatory submissions,...