15 ott - Campo di Ne
MIRA
Mira, a fast-growing femtech company, seeks a Regulatory Submission Specialist to lead and support regulatory documentation for in vitro diagnostic devices. 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.
17 ott - Bologna
Relizont S. P. A.
17 ott - Milano
SATUR
17 ott - Lombardia
Privato
17 ott - Minerbe
ORIENTA