Teleflex in Athlone, Ireland is seeking a Regulatory Affairs professional responsible for coordinating and managing regulatory and product registration activities in the EMEA region.
The candidate will prepare registration files, ensure compliance with international regulations, and provide regulatory input for projects.
A degree in a relevant Science or Engineering discipline, along with 2-3 years of medical device industry experience, is essential.
This role calls for excellent communication and project management skills, along with a good understanding of EU regulations.
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