RAQA Specialist

New Opportunity Regulatory & Quality Affairs Specialist Medical Devices Paris

Are you passionate about innovation in healthcare? Ready to make a real impact in the MedTech world?

A fast-growing medical device company based in Paris is looking for a Regulatory & Quality Affairs Specialist to support the development and commercialization of cutting-edge Class IIb/III technologies in Europe and the US (CE Marking & FDA).

Your Mission
Manage regulatory submissions (EU/FDA)
Support quality system maintenance & improvement (ISO 13485)
Contribute to Post-Market Surveillance, Risk Management & Usability
Represent RAQA in cross-functional product development teams

You Bring
3+ years of experience in RA/QA for medical devices
Strong knowledge of MDR 2017/745, ISO 13485, ISO 14971
Fluency in English & French
Experience in electromechanical or robotic devices = big plus!

Why Join?
Youll work on a meaningful innovation aiming to restore mobility and autonomy for people with disabilities, in a collaborative and fast-paced environment.

CDI | Based in Paris | Flexible hybrid policy

Interested or know someone great for this role? Lets talk!
monia@talentssolutions.fr