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Human Factors Design Engineer II

Job in North Haven, New Haven County, Connecticut, 06473, USA
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
Salary/Wage Range or Industry Benchmark: 35 - 50 USD Hourly USD 35.00 50.00 HOUR
Job Description & How to Apply Below

Human Factors Design Engineer II

Location:

Boston, MA, USA (with opportunities to support global programs).

Compensation

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.

Employment

Contract – 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.
Qualifications
  • 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.
Benefits
  • Medical Insurance
  • Vision Insurance
  • 401(k) Plan
  • Disability Insurance
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