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.
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 sigmar.ie
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