Design, development, manufacturing and post-market roles across therapeutic and diagnostic medical devices.
293 roles found · page 5 of 12
Stryker · Fort Lauderdale, FL
Edwards Lifesciences · USA Irv-1442 Alton/mic
Danaher · Remote
Danaher · Westborough, MA
Amgen · New Albany, OH
Danaher · Cardiff, UK
Stryker · Bengaluru, India
Danaher · Mannheim, Germany
Danaher · Karnataka, India
Stryker · Ventura, CA
Stryker · Dallas, TX
Stryker · Gurugram, India
Stryker · Mexico City, Mexico
Stryker · Singapore
Edwards Lifesciences · Singapore
Stryker · Gurugram, India
Medtronic · Mounds View, MN +1 more
Danaher · Cincinnati, OH
Abbott · Hamburg, Germany
Medtronic · Bulgaria
IQVIA · Durham, NC +1 more
Edwards Lifesciences · Singapore
Stryker · Gurugram, India
Stryker · Fremont, CA
Stryker · Portage, MI
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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