12 ott - Uri
MIRA
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.
#J-*****-Ljbffr
24 ott - Teramo
Abbott
24 ott - Tribiano
Adecco (Italy)
24 ott - Tivoli
AIR
24 ott - Vicenza
Ms C Group