Senior Regulatory Affairs Lead – Med Device FDA Submissions

il y a 15 heures


Les Ulis, France elemed Temps plein

A healthcare technology firm is seeking a Senior Regulatory Affairs Consultant to develop and execute regulatory strategies compliant with global requirements. The role requires leading FDA submissions and managing design controls. Ideal candidates should have 5-7 years of experience in regulatory affairs for medical devices and a good level of English. This is an exciting opportunity to be part of a midsize innovative company in the medical equipment sector. Applications can be sent via email.
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