Job Description
KEY RESPONSIBILITIES
Regulatory Affairs
Prepare, submit, and obtain approvals for medical device licenses and other relevant permits from the Taiwan authorities for assigned products.
Coordinate and maintain correspondence with Corporate Regulatory Affairs and Subject Matter Experts.
Manage and track project status using company systems and tools (e.g., WindChill).
Maintain and update any local registration strategic planning documents and meeting materials.
Provide support to direct supervisor and RA team with assigned tasks and activities.
Maintain an awareness of local regulatory requirements that impact Abbott products throughout the product life cycle.
Assesses product changes and take necessary actions to make sure product compliances.
Relationships
Build and maintain positive and collaborative relationships with internal cross fu...
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