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Senior qa & regulatory affairs specialist (mdr/iso 13485)

Dublin
ResMed Inc
Regulatory affairs specialist
Posted: 11 December
Offer description

A leading healthcare solutions company in Dublin is seeking a Senior QA/RA Specialist to ensure quality management systems meet regulatory standards. The role involves collaborating with various teams to drive regulatory strategies for product lifecycle submissions, maintaining compliance for medical devices, and overseeing quality management activities. The ideal candidate will have a technical background with a bachelor's degree and experience in ISO 13485 and MDR-related projects. This position offers the opportunity to shape quality initiatives in a global organization.
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