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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:
6/10/2024
Remote Work Level:
Option for Remote
Location:
Dublin, IrelandJob Type:
Employee
Job Schedule:
Full-Time
Career Level:
Experienced
Travel Required:
No specification
Categories:
Company:
Company details here
Benefits:
Company Benefits here
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