Regulatory Affairs Lead, Medical Devices (France/EMEA)

Abbott in France (Rungis) seeks a Regulatory Affairs Senior Specialist to lead regulatory activities across the EMEAP region, focusing on France. You will drive regulatory strategy, ensure compliance with global and local requirements, and support lifecycle management of diabetes care products in a matrixed international environment.

Responsibilities include preparing technical documentation for CE marking, in-country submissions, and advising cross‑functional teams on MDR/IVDR compliance.