Teleflex is seeking a Regulatory Affairs Specialist to support regulatory activities for medical products in the EMEA region.
Responsibilities include managing regulatory submissions, ensuring compliance with EU regulations, and providing support during audits.
Successful candidates will possess a degree in a Science or Engineering discipline, have 2-3 years' experience in the medical device industry, and demonstrate strong communication and organizational skills.
The role is on-site in Athlone, Ireland.
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