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 adecuado candidate has experience in regulatory submissions, technical documentation, and international IVD regulatory requirements, with strong writing, project management, and cross-functional coordination
📌 Remote Regulatory Submission Lead – Ivd (Valladolid)
🏢 Mira
📍 Valladolid
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.