Design, development, manufacturing and post-market roles across therapeutic and diagnostic medical devices.
77 roles found · page 4 of 4
Ginkgo Bioworks · Emeryville, California
Abbott · Germany - Hesse - Eschborn
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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