Regulatory Affairs Specialist

AbbVie

Taipei, Taiwan
Medical device license submission
Regulatory compliance management
Project status tracking tools
Prepare, submit, and obtain approvals for medical device licenses and other relevant permits from Taiwan authorities for assigned products

Job Summary

  • Prepare, submit, and obtain approvals for medical device licenses and other relevant permits from Taiwan authorities for assigned products.
  • Build and maintain positive and collaborative relationships with internal cross functions and external regulatory agencies to support business and compliance objectives.
  • Develop and implement action plans for self and team to ensure efficient and timely completion of objectives.

Matching Summary

Prepare, submit, and obtain approvals for medical device licenses and other relevant permits from Taiwan authorities for assigned products.

Skills & Requirements

Must-have

  • Medical device license submission
  • Regulatory compliance management
  • Project status tracking tools
  • Local regulatory requirements awareness
  • Cross-functional collaboration
  • Microsoft Office proficiency

Nice-to-have

  • Good interpersonal skills
  • Adaptable to complex tasks
  • English communication skills

Key Requirements

  • Bachelor’s or master’s degree in science or engineering
  • English writing, speaking, listening, and reading skills

Work Rights

Not specified

Tailored Resume

Cover Letter