28 ott - Genova
MIRA
Mira, a San Francisco-based hormonal health company, seeks a Regulatory Submission Specialist to lead regulatory documentation for IVD devices.
La descrizione completa del lavoro illustra tutte le competenze, l'esperienza pregressa e le qualifiche che i candidati dovrebbero possedere.
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. xlwpduy
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Per questa posizione sono disponibili opzioni di lavoro a distanza/a casa.