Global Medical Device Regulatory Specialist

A medical device consulting company located in Seattle is seeking a Regulatory Affairs Specialist to prepare regulatory submissions for medical devices. Applicants must hold a B.S. in a life science or technical field and have 2-5 years of Medical Device experience. The role demands strong problem-solving abilities and attention to detail, with proficiency in Microsoft Office. Familiarity with FDA regulations and EU Notified Bodies is critical for ensuring compliance and successful product registrations. J-18808-Ljbffr