Senior Regulatory Compliance Specialist Medical Device
Oracle · United States
Full-timeOn-sitePosted 13 June 2026
Apply on Company Site →Job description
We are seeking a detail-oriented Senior Compliance Specialist to support our medical device development organizations in complying with global regulatory requirements including CE marking for the European Union (EU MDR), Medical Device Single Auditing Program (MDSAP), ISO 9001:2015, and ISO 13485:2016 certifications, as well as other international medical device regulations.
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