Regulatory & Quality Engineer, SaMD (3-Month)

Avicenna.AI seeks a Quality & Regulatory Affairs Engineer for a 3-month assignment to support CE marking, FDA submissions, and maintenance of ISO 13485 QMS. You will collaborate with Regulatory, Quality, Clinical, Production, R&D, Marketing and Product teams, plus distributors.

The role requires a Master's in a scientific field, 3+ years in regulatory affairs for medical devices, and strong English. Hybrid work is offered with La Ciotat offices; contract is fixed-term and renewable.