Hfe Co-op (fall 2026)

Johnson & Johnson Johnson & Johnson · Pharma · Raritan, NJ +1

Johnson & Johnson is seeking a Human Factors Engineering Co-op to support the design and evaluation of user interfaces for medical products. The role involves conducting contextual research, creating usability specifications, and testing with stakeholders to ensure safe, effective, and satisfying use of medical devices. The co-op will contribute to usability documentation and analysis, working closely with product development teams.

What you'd actually do

  1. Leverage human factors standards and best practices to inform new product designs and ensure concepts support safe, effective, and satisfying use
  2. Support the planning, conduct, and reporting of various user research activities, including ethnography, focus groups, formative usability tests, and HF validation (summative usability) tests
  3. Consolidate user feedback into meaningful design insights and actionable recommendations
  4. Perform thoughtful and thorough root cause analysis for use-related problems that arise during hands-on usability tests
  5. Understanding the use environments and participating in the creation of user workflows

Skills

Required

  • Enrolled in a college/institution pursuing a bachelor’s or master’s degree in Human Factors Engineering, Usability Engineering, Cognitive Science, Psychology, Mechanical Engineering, or Biomedical Engineering
  • Authorized to work in the United States and not require sponsorship in the future
  • Availability for at least a 4-month co-op rotation
  • Minimum GPA of 3.0
  • Understanding of the research process (planning, execution, analysis and documentation)
  • Knowledge of human factors and design principles
  • Working knowledge of task and risk analysis methods, human perception, and cognition
  • Basic knowledge of anthropometrics, biomechanics and physiology
  • Experience consolidating user feedback into concise, meaningful design insights and actionable recommendations

Nice to have

  • Design project experience or user centered research is preferred
  • Experience performing root cause analysis for use-related problems is preferred
  • Familiarity with FDA, ISO, AAMI, and other relevant usability regulations and standards for medical devices is highly preferred

What the JD emphasized

  • FDA, ISO, AAMI, and other relevant usability regulations and standards for medical devices is highly preferred