Global Medical Devices Regulatory

Il y a 5 jours

Paris, Île-de-France ProductLife Group Temps plein

ProductLife Group is seeking a Medical Device Associate to support regulatory and quality activities for medical devices across international markets, helping ensure compliance with MDR, IVDR, ISO 13485, and related standards while contributing to a wide range of client projects.

In this role you will prepare and maintain technical documentation, reviews of labeling, CAPA processes, and participate in audits.

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