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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