Design, development, manufacturing and post-market roles across therapeutic and diagnostic medical devices.
293 roles found · page 10 of 12
Becton Dickinson · Covington BMD
Medtronic · Croatia +2 more
Medtronic · Vietnam
Becton Dickinson · Davis Drive +1 more
Medtronic · Mounds View, MN
Medtronic · Czech Republic
Medtronic · Tokyo, Japan
Medtronic · Mounds View, MN +1 more
Medtronic · Romania
Becton Dickinson · Anasco
Medtronic · Tokyo, Japan
Medtronic · Berlin, Germany
Medtronic · Finland
Medtronic · Slovakia
Medtronic · Silesia, Poland +1 more
Regeneron · Tech Valley
Becton Dickinson · Covington BMD
Medtronic · North Haven, CT
Becton Dickinson · Covington BMD +2 more
Stryker · Cary, IL
Stryker · San Jose, CA
Stryker · Berkshire +8 more
Edwards Lifesciences · Singapore
Edwards Lifesciences · Irvine, CA
Stryker · Cincinnati, OH +2 more
Medical device work runs on its own regulatory and engineering track: design controls under 21 CFR 820.30, risk management to ISO 14971, a quality system to ISO 13485, and post-market surveillance obligations that intensified under the EU MDR. Roles span R&D and design engineering, verification and validation, human factors, manufacturing and process engineering, and field clinical support. Software as a medical device has made regulatory-aware software and cybersecurity engineering a growing part of this category rather than a niche within it.
Roles in this area are also listed as medtech jobs, device engineering jobs, ISO 13485 jobs and design assurance jobs.
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