Descripción de la oferta
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
