Senior Global Regulatory Affairs Manager - Medical Devices

eTeam is seeking a qualified candidate to manage regulatory documentation and support international registrations for medical devices in New Jersey. The ideal candidate will exhibit competence in US and foreign regulations, possess strong project management skills, and handle proprietary information confidentially.

Applicants should have a bachelor’s degree in science or biomedical engineering, with 4–6 years of relevant experience in regulatory activities. An advanced degree and RAC Certification are desirable, with evidence of foreign regulatory approvals being a plus.