Global Medical Device Regulatory

Il y a 3 jours

Courbevoie, Île-de-France ProductLife France Temps plein 55 000 € - 75 000 € Contrat

ProductLife Group is seeking a Medical Device Associate to support regulatory and quality activities for medical devices across international markets. You will work on MDR/IVDR compliance, Technical Documentation, CAPA, and audit support in a dynamic global team.

The role requires a Life Sciences degree, experience in regulatory affairs, and fluency in French and English. Hybrid & flexible working is offered with continuous learning opportunities and international exposure.