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HFE Intern Raritan

Job in Raritan, Somerset County, New Jersey, 08869, USA
Listing for: Antler
Apprenticeship/Internship position
Listed on 2026-09-20
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 32000 - 72000 USD Yearly USD 32000.00 72000.00 YEAR
Job Description & How to Apply Below
Position: HFE Intern Raritan Spring 2027

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

About Med Tech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at

Description

The Johnson & Johnson Medical Devices (JJMDC) Industrial Design, Human Factors, User Exprieence (IDHF/UX) organization is seeking a multi-faceted, exceptionally talented, user-centered Human Factors Engineer (HFE) who is passionate about improving the quality of people's lives through compelling design experiences.

Our team leads contextual research to discover unmet user needs, creates usability specifications and requirements, and iteratively tests with stakeholders throughout a robust usability process. The position will interact closely with the product development team to design and evaluate user interfaces (hardware and software) for medical products including devices, support systems and associated training /instructional elements. We are a diverse, collaborative, and global team, striving to create products and solutions that improve patient outcomes by delivering remarkable user experiences.

The successful candidate will continue to elevate world-class human factors approaches throughout the organization while providing timely usability insight to the product development teams.

This position will be based at our Raritan, NJ office and will report directly to the IDHF/UX team at those locations for the period of January to May 2027
. It is expected that the co-op works on-site at this location, in person. Housing will not be provided by Johnson & Johnson, but rather a one-time stipend may be offered to qualified candidates.

Key Responsibilities
  • Leverage human factors standards and best practices to inform new product designs and ensure concepts support safe, effective, and satisfying use.
  • Support the planning, conduct, and reporting of various user research activities, including ethnography, focus groups, formative usability tests, and HF validation (summative usability) tests.
  • Consolidate user feedback into meaningful design insights and actionable recommendations.
  • Perform thoughtful and thorough root cause analysis for use-related problems that arise during hands-on usability tests.
  • Understanding the use environments and participating in the creation of user workflows.
  • Understand the regulatory imperative for medical device human factors, including relevant human factors standards and guidance documents, such as IEC 62366 and FDA's final HF guidance.
  • Contribute to human factors documentation, including formative and summative test plans and reports, expert reviews, use-related risk analyses, use specifications, known problems analyses, and Human Factors Engineering reports
  • Author study documentation (e.g., informed consent forms, study participant recruitment screeners, moderator's guides, use error checklists).
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