Oracle
Senior Regulatory Compliance Specialist Medical Device
United States
Company's own board
First seen Oct 24 · seen live today · from Oracle's own Oracle Cloud board
The posting, as published
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.