Bachelor’s degree or above
No less than five years’ experience in Medical Device compliance or regulatory affairs
Have comprehensive knowledge of medical device classification and compliance.
Excellent problem solving and communication skills.
Ability to plan and schedule multiple priorities in a concurrent fashion
Ability to work well within cross-functional teams
Good written and oral English
Proficient in Microsoft applications

Serve as the “gate keeper” of the company’s daily distribution activities
Responsible for screening the products and identify the medical devices and other regulated items if necessary
Provide regulatory inputs to ensure regulatory compliance and to optimize the relevant processes
Responsible for maintaining the gate keeping documentation
Support RA projects as required
Support department special projects as required