In charge of regulatory approval and product registration
Communicate with regulatory authorities as well as overseas counterparts with regards to regulator affairs matters such as product registrations, changes in existing products and renewals
Advise internal stakeholders on regulatory guidelines
In charge of new product registration and license renewal progress
Maintain and update business agreements with overseas counterparts
Any other adhoc duties pertaining to regulatory affairs
Requirements
Possess bachelor's degree in related field
At least 3 years of relevant work experience
Good knowledge of Medical Devices and cosmetics regulatory guidelines
Good knowledge of Microsoft Office applications.
EA License No: 13C6305
Reg. No.: R1989581
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