Global Regulatory Affairs Lead - Medical Devices (510/CE)

A leading medical device consultancy based in Omaha, Nebraska is seeking a Regulatory Affairs Level III specialist to manage global product registrations and ensure compliance within the medical device industry. The ideal candidate has over 5 years of regulatory affairs experience and must have a strong background in leading successful FDA 510(k) clearances and CE marking for respiratory devices. Excellent analytical, communication, and detail-oriented skills are essential for this role. #J-18808-Ljbffr