Human Factors Design Engineer II
Job in
North Haven, New Haven County, Connecticut, 06473, USA
Listed on 2026-01-15
Listing for:
Redbock - an NES Fircroft company
Full Time
position Listed on 2026-01-15
Job specializations:
-
Engineering
Biomedical Engineer, Medical Device Industry, Quality Engineering
Job Description & How to Apply Below
Human Factors Design Engineer II
Location:
Boston, MA, USA (with opportunities to support global programs).
Base pay range: $35.00/hr - $50.00/hr (actual pay based on skill and experience). This range is provided by Redbock — an NES Fircroft company.
EmploymentContract – Mid‑Senior level.
Responsibilities- Plan, conduct, and document usability testing in a medical device use context.
- Plan, scale, document, and execute human factors program activities in accordance with FDA guidance and international standards (e.g., IEC 62366, IEC 60601, ISO 14971).
- Perform use‑related risk analysis and document findings.
- Design usability studies and drive testing strategies, including simulation of product właśnie use for user needs investigation, concept selection, and requirement development.
- Moderate usability testing of prototypes with end users and customers, and conduct contextual inquiries for applicable use cases/environments (e.g., surgery).
- Assist in data collection and root‑cause analysis during usability testing.
- Provide technical insight for user interface design, human factors processes, and planning for team and business strategy.
- Contribute to and maintain human factors program documentation as part of the Usability Engineering File.
- Support preparation of usability‑related documentation for regulatory submissions.
- Identify use‑related issues upon post‑market launch and recommend risk‑control enhancements.
- Formulate, deliver, and manage projects; mentor colleagues or direct lower‑level professionals when required.
- Bachelor’s degree in Human Factors, Biomedical Engineering, Industrial Design, Industrial Engineering, or closely related field.
- At least 2 years of practical experience; alternatively a Master’s degree or higher with 0 years of experience (preferably with specific experience in medical device development).
- Demonstrated competence in human factors practice, including knowledge of FDA guidelines and international standards.
- Medical Insurance
- Vision Insurance
- 401(k) Plan
- Disability Insurance
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