EMEA Regulatory Submissions Lead

A leading medical device company in Île-de-France is seeking an EMEA International Registration Manager. This role involves managing product registrations, ensuring compliance with regulations, and supporting the development of medical devices. The ideal candidate should have 4-5 years of experience in regulatory affairs, exceptional communication skills, and a relevant master's degree. This position offers a unique opportunity to contribute to the healthcare sector while working in a dynamic and innovative environment.

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