28 ott - Genova
MIRA
Mira, a fast-growing femtech company, seeks a Regulatory Submission Specialist to lead and support regulatory documentation for in vitro diagnostic devices.
Le informazioni riportate di seguito illustrano i requisiti del ruolo, l'esperienza richiesta ai candidati e le qualifiche associate.
You will ensure compliance across technical documentation and regulatory programs while collaborating with internal teams and external consultants.
The role emphasizes EU IVDR CE-marking readiness, post-market surveillance, and cross-functional coordination in a remote, fast-paced startup environment that serves a global market.
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