Senior Regulatory Affairs Specialist Contractor

Job description

Multinational Medical Device Manufacturer requires a contractor for a Senior Regulatory Affairs position for minimum of 12 months. Hourly Rate role.

**Experience with submissions in the EU to a Notified body and in the US to FDA is required**

Purpose of the Role:

Responsible for Regulatory Affairs support of the site, submissions and regulatory compliance.

Minimum Requirements:

BSC/BEng Degree

Experience in MDD, MDR, FDA, ISO environment

Ability to identify and drive regulatory compliance improvements

Excellen communication skills

For more information and to see a full job description, please call Sarah on 091 455301 or email shayes at

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