PQE Group is seeking an experienced Quality Assurance & Regulatory Affairs professional to support a Medical Device organization.
Para una comprensión completa de esta ocasión y de lo que se requerirá para ser un candidato exitoso, siga leyendo.
You will act as an extension of the manufacturer's quality and regulatory team, ensuring compliance with EU MDR 2017/745 and ISO 13485/9001/14001.
The role involves hands-on quality and regulatory activities across audits, CAPAs, deviations, and post-market xghoner surveillance, with opportunities to collaborate on international projects and product registrations.
📌 Senior QARA Specialist – MedTech Compliance (Barcelona)
🏢 Pqe Group
📍 Barcelona
Postulate a este anuncio
Muestra tus habilidades a la empresa, rellenar el formulario y deja un toque personal en la carta, ayudará el reclutador en la elección del candidato.