Global Regulatory Affairs Device Lead - Cambridge

Only for registered members Cambridge, United States

1 month ago

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Job summary

The Global Regulatory Affairs Device Lead will drive global regulatory strategies for medical device and combination products.

We are seeking an experienced Regulatory Affairs professional with familiarity with international submissions from within a global healthcare organization.


Responsibilities

  • Serve as GRA Device Lead on assigned project teams
  • Provide regulatory guidance and advice to Global Regulatory Team (GRT) and cross-functional teams

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