Opportunity to join a global orthopedic company and lead their APAC Regulatory activities.
Responsibilities
- Lead and manage day to day activities and corporate APAC regulatory staff;
- Support regulatory activities that lead to and maintain regulatory compliance and approval for Arthrex devices in APAC;
- Work closely with regional APAC regulatory team to develop and drive process efficiencies for APAC regulatory submissions.
Education and Experience:
- Advanced Degree (MS or PhD, or equivalent) preferred; preferably in a Science or Engineering discipline.
- 5 years direct experience in Regulatory Affairs in a Medical Device Company required. Orthopedics preferred