EU MDR Compliance Lead – Medical Device Quality
Listed on 2026-11-05
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Quality Assurance - QA/QC
Oracle Health seeks a Senior Compliance Specialist to guide cross‑functional teams on medical device quality system compliance, focusing on CE marking and EU MDR requirements. The role covers conformity assessment, documentation, risk management, and post‑market surveillance.
Responsibilities include audits coordination, CAPA, regulatory monitoring, HQMS data analysis, and supplier quality support, with collaboration across the business.
Our group is growing, and we are hiring a EU MDR Compliance Lead – Medical Device Quality in Santa Fe, NM, United States.
As a EU MDR Compliance Lead – Medical Device Quality, you will play an important part at Oracle in Santa Fe, NM, United States.
We invite applications for the EU MDR Compliance Lead – Medical Device Quality position located in Santa Fe, NM, United States.
The following position is for a EU MDR Compliance Lead – Medical Device Quality with Oracle.
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