RAQA Specialist
RAQA Specialist
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Job Description
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 fastgrowing medical device company based in Paris is looking for a Regulatory & Quality Affairs Specialist to support the development and commercialization of cuttingedge 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 PostMarket Surveillance Risk Management & Usability
Represent RAQA in crossfunctional 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 fastpaced environment.
CDI Based in Paris Flexible hybrid policy
Employment Type
Full Time
