Regulatory Affairs Specialist (Medical Tools)
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Requirements:
* Candidates understand the process of AKD registration with type three Active Medical Device.
* Ability to obtain permits quickly and effectively, regardless of circumstances. (Get-it-done person)
* Strong connections with the Ministry of Health, particularly in relation to AKD permits.
* Ability to work independently as a single contributor.
* Fluent in English (proficiency in Mandarin is a plus).
* Reports directly to the Deputy General Manager.
Job Description :
* Understand the registration system for local medical devices.
* Responsible for the preparation and execution of product registration plans, and have project management capabilities to promote the on-schedule progress of registration projects.
* Track the registration process and solve various problems raised by MOH in a timely and effective manner.
* Navigate the AKD process efficiently and secure the AKD approval promptly.