Senior Human Factors Engineer, Medical Robotics Usability

Johnson & Johnson MedTech

Cincinnati (OH)

On-site

USD 92,000 - 148,000

Full time

4 days ago
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Job summary

Johnson & Johnson MedTech is recruiting a Senior Human Factors Engineer to lead HF activities for the OTTAVA Robotic Surgical System. This role will collaborate with R&D, Marketing, Regulatory, Clinical, and Quality teams to ensure user-centric design and safe, effective products.

You will deliver HF strategies across product lines, mentor engineers, and guide third-party contractors. A strong background in medical device development and regulatory standards is required, with up to 20% travel

Qualifications

  • Minimum 5 years in human factors/usability engineering for medical devices.
  • Proficient in HF process, research, risk assessment, user interface requirements, and regulatory submissions.
  • Ability to negotiate with stakeholders and provide disposition feedback for risk management documentation.
  • Experience in planning, executing, documenting, and reporting usability testing, including moderation.

Responsibilities

  • Support the development and execution of human factors and usability strategies from concept through post-market support.
  • Collaborate with cross-functional teams to design, evaluate, and guide solutions with user impact in mind.
  • Prepare usable engineering documents: task analyses, usability risk assessments, use specs, test reports and root cause analyses.
  • Mentor other engineers and supervise third-party contractors.

Skills

Human Factors
Regulatory Submissions
Usability Testing
Risk Management
User Interface
IEC 62366
ISO 14971
Medical Devices
Travel Ability

Education

Bachelor's Degree in Human Factors / Usability / Biomedical Engineering

Job description

Johnson & Johnson MedTech is recruiting a Senior Human Factors Engineer to lead HF activities for the OTTAVA Robotic Surgical System. This role will collaborate with R&D, Marketing, Regulatory, Clinical, and Quality teams to ensure user-centric design and safe, effective products.

You will deliver HF strategies across product lines, mentor engineers, and guide third-party contractors. A strong background in medical device development and regulatory standards is required, with up to 20% travel

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