Design, development, manufacturing and post-market roles across therapeutic and diagnostic medical devices.
293 roles found · page 12 of 12
Stryker · Ventura, CA
IQVIA · Madrid, Spain
Agilent · Japan-remote Location
Stryker · Waltham, MA
Stryker · Portage, MI
Stryker · Gurugram, India
Stryker · Gurugram, India
Illumina · Northtech, Singapore
Illumina · San Diego, CA
Centrillion Biosciences · Palo Alto, CA
Ginkgo Bioworks · Emeryville, CA
Abbott · Porto
Abbott · Milan, Italy +2 more
Abbott · Madrid, Spain
Abbott · Remote
Abbott · Milan, Italy +2 more
Abbott · Milan, Italy +2 more
Abbott · Milan, Italy +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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