Medical device jobs

About medical device roles

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.

Common job titles

• R&D Engineer, Medical Devices
• Design Assurance Engineer
• Verification & Validation Engineer
• Human Factors Engineer
• Field Clinical Engineer
• Post-Market Surveillance Specialist

Also searched for

Roles in this area are also listed as medtech jobs, device engineering jobs, ISO 13485 jobs and design assurance jobs.