Engineering Co-op - Human Factors

Arthrex

1d•Onsite

About The Position

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a student pursuing a career in medical device design and development to support the Human Factors Engineering team in Naples, FL. The Human Factors Engineering team is responsible for supporting human factors engineering activities for medical device development projects and regulatory submissions across Arthrex. The ideal candidate would be pursuing a degree in Biomedical or Mechanical Engineering, Human Factors Engineering, Industrial Engineering, Cognitive Psychology or Industrial Design. Job activities/responsibilities may include, but are not limited to, usability documentation creation, complaints analyses, assisting in risk analyses and usability testing. The individual will also work within the requirements of their tasks to deliver results and communicate issues in a timely, detailed and accurate manner. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™. This Co-op will run from July 2026 – December 2026. The ideal candidate will have the availability to work 40 hours per week at our Naples, FL facility. Main Objective: To support the Human Factors Engineering team in various responsibilities and deliverables, while learning about medical device design processes and procedures.

Requirements

Enrolled as a full-time student pursuing a bachelor’s or master's degree or recent graduate within the last six months required.
Junior or above, pursuing a degree in Human Factors, Industrial Design, Biomedical, Mechanical, Industrial Engineering or Cognitive Psychology preferred.
(Recent graduates must be within six months of their graduation date to qualify.)
Basic to intermediate computer skills.
Be able to follow written and verbal direction.

Nice To Haves

Knowledge about design controls or the medical device development process preferred.

Responsibilities

Generate or assist in generating human factors engineering reports and documentation for regulatory submissions, such as Medical Device Regulation (MDR) remediation/resubmissions.
Assist in human factors analyses, such as complaints analyses, task analyses and risk analyses.
Assist or participate in the planning, execution and review of usability testing of devices or concepts for various development projects.
Other duties as assigned.