Medical Device Compliance Specialist

2 weeks ago


Ennis, Clare, Ireland Cregg Group Full time

**About the Role**

In this key role, you will provide regulatory direction to development project teams as a core team member and advise other functional units on the requirements in each target market.

You will review proposed labeling and instructions for use for compliance with applicable local and international regulations and recommend changes for labelling and internal documentation.

This is an excellent opportunity to become the Subject Matter Expert (SME) for the Biological safety process and work closely with Regulatory and Clinical Affairs to address biological aspects for submissions to EU/US regulators.



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