Regulatory Affairs Specialist

Regulatory Affairs Specialist is responsible for obtaining approvals and registrations of our mission-critical products in S. Korea and ASEAN countries. Person in this role will coordinate with regional counterparts on products to maintain up-to-date information on local regulatory requirements. The incumbent’s medical device regulatory expertise, organizational ability, and multi-tasking skills will be rewarded with opportunities for career growth and advancement in a company that makes a difference in people’s lives. The ideal candidate brings strong regulatory expertise, attention to detail, and the ability to manage multiple priorities in a fast-paced environment.