17 oct
|
Mira
|
Barcelona
Mira seeks a Regulatory Submission Specialist to lead regulatory documentation for IVD devices.
Maximice sus posibilidades de que su candidatura sea seleccionada asegurándose de que su CV y sus habilidades se ajustan al perfil.
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. xhfqzwm
The idóneo candidate has experience in regulatory submissions, technical documentation, and international IVD regulatory requirements, with strong writing, project management, and cross-functional coordination
Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.
📌 Remote Regulatory Submission Lead – Ivd (Barcelona)
🏢 Mira
📍 Barcelona