Human Factors Engineer

3 weeks ago


Santa Clara, United States Johnson & Johnson Full time

Johnson & Johnson MedTech is recruiting for a Human Factors Engineer, located in Santa Clara, CA.

At Johnson & Johnson MedTech, we're changing the trajectory of health for humanity, using robotics to enhance healthcare providers' abilities and improve patients' diagnoses, treatments, and recovery times. Johnson & Johnson Robotics was established in 2020 with the integration of Auris Health, Verb Surgical, C-SATS, and Ethicon. It comprises three key med-tech platforms: Flexible Robotics (MONARCH), Surgical Robotics (OTTAVA), and Digital Solutions. Join our collaborative, rapidly growing teams in the San Francisco Bay Area (Redwood City and Santa Clara), Cincinnati, and Seattle. You'll collaborate on breakthrough medical technologies that unite multiple subject areas to build a connected digital ecosystem that advances medical professionals' skills and improves patient outcomes.

Overview

You will join the Human Factors & Experience Design (HFXD) team and help shape OTTAVA, Johnson & Johnson's new surgical robotic system.

As a Human Factors Engineer, you will contribute to Human Factors workstreams that are essential to the success of Ottava. You will contribute to usability activities with mentorship from lead Human Factors Engineers. You will work in close partnership with your colleagues to meet program objectives, using your disciplinary knowledge and passion for safety and usability to inform key design decisions

Our collaborative culture heavily emphasizes growth and development and you'll receive mentorship from HF leads to help develop your skillsets and advance your career.

Does the idea of working in medical robotics excite you? Are you an emerging professional who is motivated by impacting patients globally with your work? If so, we'd love to hear from you

Responsibilities:

* Support human factors work, using best-in-class methodologies to inform rigorous decision-making
* Support product submission deliverables
* Act as a contributor on human factors methodologies
* Apply knowledge of FDA, ISO, AAMI and other relevant regulations and standards



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