Global Medical Device Regulatory

Il y a 2 jours

Courbevoie, Île-de-France ProductLife Group Temps plein 50 000 € - 70 000 € Contrat

ProductLife Group, a global regulatory and quality consulting leader, seeks a Medical Device Associate to support regulatory and quality activities for medical devices international markets. You will contribute to regulatory registrations, CAPA processes, and documentation updates, collaborating with cross-functional teams worldwide.

Ideal candidates hold a Life Sciences degree and have experience with MDR/IVDR, ISO 13485, and technical documentation, plus fluency in French and English.