Description:
The Technical Writer will ensure the clarity, accuracy and quality of our medical device quality documents, ensuring compliance with US pre-market regulatory submission requirements (e.g., FDA 510(k), De Novo). The Technical Writer will collaborate across hardware, software, and catheter development teams to document complex technical information in accordance with procedures and standards. This role is based full-time in our Burlington, MA office. ResponsibilitiesAct as a subject matter expert
Jan 23, 2026;
from:
dice.com