Specialist, Regulatory Affairs

Edwards Lifesciences

Beijing, China
Experience in regulatory submissions
Ability to manage confidential information
Attention to detail
Make a meaningful difference to patients around the world

Job Summary

  • Make a meaningful difference to patients around the world.
  • Support management of processes to obtain and evaluate document finalization.
  • Serve as regulatory and clinical science liaison throughout product lifecycle.

Matching Summary

Make a meaningful difference to patients around the world.

Skills & Requirements

Must-have

  • Experience in regulatory submissions
  • Ability to manage confidential information
  • Attention to detail

Nice-to-have

  • Problem-solving and critical thinking skills
  • Excellent communication skills
  • Teamwork and collaboration

Key Requirements

  • Bachelor's Degree in related field
  • 3 Years’ experience in regulatory affairs
  • Full knowledge of regulatory guidelines

Work Rights

Not specified

Tailored Resume

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