Regulatory Affairs Specialist

Manage global regulatory affairs requirements, prepare and project manage device registrations for approval by the US FDA and EU Competent Authorities, liaise with regulatory authorities, and contribute to the development of the Regulatory Strategy.

• Date Posted:

  5/11/2024 

• Remote Work Level:

  Option for Remote

• Location:

  Dublin, Ireland

• Job Type:

  Employee

• Job Schedule:

  Full-Time

• Career Level:

  Experienced

• Travel Required:

  No specification

• Categories:

  Research, Medical & Health, Project Management

• Company:

  Company details here

• Benefits:

  Company Benefits here

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