Remote Regulatory Submission Lead – IVD

Hace 22 horas

barcelona, cataluña, España Mira Jornada completa

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, technical documentation, and international IVD regulatory requirements, with strong writing, project management, and cross-functional coordination

#J-18808-Ljbffr