Global Regulatory Affairs Specialist - Medical Devices

A leading healthcare products company located in Schaumburg, Illinois, is seeking a Regulatory Affairs Specialist to coordinate and submit regulatory applications for medical devices across various regions including the US, Canada, and Latin America. The ideal candidate will have a BS degree and at least 3 years of relevant experience in the regulatory compliance of medical devices. This role includes writing 510(k) submissions and ensuring compliance with regulations.

Strong communication and organizational skills are essential for success.
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