Mira, a San Francisco-based hormonal health company, seeks a Regulatory Submission Specialist to lead regulatory documentation for IVD devices. You will ensure evidence supports claims, align labeling, and coordinate with internal teams and external consultants to maintain compliance throughout the product lifecycle.
The role requires EU IVDR experience, strong technical writing, and the ability to work in a fast-paced startup while collaborating across global teams.
📌 Remote Regulatory Submission Lead – EU IVDR/CE for IVDs (Bardi)
🏢 MIRA
📍 Bardi
Candidati a questo annuncio
Mostra le tue capacità professionali all'azienda, compila il form e lascia un tocco personale nella lettera di presentazione, aiuterà il recruiter nella scelta del candidato.