Sr RA specialist

? 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