01 nov
|
Mira
|
Barcelona
Mira seeks a Regulatory Submission Specialist to lead regulatory documentation for IVD devices.
¿Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuación.
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 idóneo candidate has experience in regulatory submissions, technical documentation, and international IVD regulatory requirements, with strong writing, project xghoner management, and cross-functional coordination
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Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.
📌 Remote Regulatory Submission Lead – IVD (Barcelona)
🏢 Mira
📍 Barcelona