EU MDR Medical Device Design & Compliance Lead
Listed on 2026-10-07
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Engineering
Medical Device Industry, Biomedical Engineer
Actalent seeks a lead engineer to drive design, development, and EU MDR 2017/745 compliance for medical devices. You will generate technical documentation, conduct risk assessments, and coordinate Notified Bodies for audits.
The ideal candidate holds a degree in Mechanical, Biomedical, or Electrical Engineering with several years of medical device R&D and strong expertise in EU MDR documentation and design controls.
We have an opening for a EU MDR Medical Device Design & Compliance Lead in Aurora, CO, United States within Engineering.
The following opening is for a EU MDR Medical Device Design & Compliance Lead with Actalent.
Our group is growing, and we are hiring a EU MDR Medical Device Design & Compliance Lead in Aurora, CO, United States.
This opening is for the EU MDR Medical Device Design & Compliance Lead role at Actalent.
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