Senior Regulatory Affairs Specialist - International

Are you looking to advance your career at one of the world's largest medical device companies?

If so I'm closely working with the International Regulatory team at a class II and III medical device company in Irvine that is looking to bring on a Senior Regulatory Affairs Specialist that will be instrumental in leading international regulatory submissions for multiple overseas markets.

Must haves:

  • Bachelor's degree in science, engineering, health care or related field
  • 5 years of experience (3 with Master's) in regulatory affairs in the medical device field
  • APAC or LATAM regulatory experience
  • Experience submitting to international notified bodies

While this role offers:

  • A competitive salary range and bonus target
  • The opportunity to be a part of a small, high achieving team with the potential for internal promotion and work on class II and III devices

Sthree US is acting as an Employment Agency in relation to this vacancy.