We are recruiting a ISO 13485 Quality Assurance / Regulatory Affairs Manager

Mission

CILIATECH is developing a new implant for glaucoma surgery, not yet commercialized.

You will be responsible for managing and adapting the quality system to meet the various standards required for international commercialization (ISO 13485, MDR 2017/745, MDSAP, FDA 21 CFR 820…), as well as preparing the necessary documentation for registrations outside Europe.

You will also be responsible for product release before market placement.

You will report directly to the R&D and Quality Assurance Manager.