Product Development Engineer – Medical Devices
Job in
Dover, Morris County, New Jersey, 07801, USA
Listed on 2026-09-14
Listing for:
Engineering Resource Group, Inc.
Full Time, Seasonal/Temporary
position Listed on 2026-09-14
Job specializations:
-
Engineering
Medical Device Industry, Biomedical Engineer, Quality Engineering
Job Description & How to Apply Below
- Permanent position for a Senior Electrical Engineer for new product development of medical devices.
- This can also be a contract/temp position position if desired. - Design, develop and verify device hardware and embedded software under design controls, for new products and revisions to existing ones.
- Support PCB development through design reviews, prototype builds, debugging and firmware implementation.
- Troubleshoot at the board level using oscilloscopes, logic analyzers and other bench instrumentation.
- Write and execute verification protocols, test methods and reports with full traceability to requirements.
- Responsible for design control deliverables including design plans, specifications, risk analyses and DHF, DMR and RMF content.
- Translate IEC requirements into engineering and product requirements.
- Serve as technical lead during FDA inspections and audits.
- Support transfer to production, manufacturing troubleshooting and test fixture development.
- Coordinate design and risk reviews with quality, regulatory, manufacturing and third-party contractors.
- BS Electrical Engineering or Biomedical Engineering (or related technical field).
- Minimum 10 years of experience in medical device product development or a related engineering role.
- Hands-on experience with PCB design, assembly and debugging.
- Experience with embedded software development.
- Experience writing verification protocols, test reports and regulator-ready technical documentation.
- Experience with domestic and international medical device regulatory requirements (FDA, EU MDR, etc.).
- Proficiency with oscilloscopes, logic analyzers and general bench test equipment.
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