Medical Device Compliance Manager - Augusta - beBeeRegulatoryAffairs

    beBeeRegulatoryAffairs
    beBeeRegulatoryAffairs Augusta

    1 week ago

    Job title: Principal Regulatory Affairs Specialist

    Description
    • Main Responsibilities:
    • Lead new and modified product development projects to establish and integrate regulatory strategy into project activities.
      Lead the preparation, submission, and maintenance of global product registrations with a focus on 510(k), EU Technical Documents, and International STEDs.
      Collaborate with internal departments to assess international registration requirements, develop international regulatory strategy, and ensure timely execution.

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