Overview
On Site
Full Time
Part Time
Accepts corp to corp applications
Contract - Independent
Contract - W2
Contract - 6 MOnth(s)
Skills
Mergers and Acquisitions
Microsoft PowerPoint
Communication
UPS
Attention To Detail
Organized
Risk Analysis
Management
Product Development
Medical Devices
Human Factors And Ergonomics
Usability
ISO 9000
Collaboration
Research and Development
Marketing
Oracle UCM
IMG
Job Details
Title : Human Factors Engineer (Medical Devices)
Location : Andover, MA ( Hybrid )
About the job We are seeking an experienced Human Factors Engineer for a 4-month contract. This role requires hands-on experience conducting usability studies with detailed Word reports (not just PowerPoint). The ideal candidate will have a strong background in authoring risk analysis documents, demonstrating proactive communication, and providing active follow-ups. The candidate should be detail-oriented and organized, able to create and adhere to schedules while delivering results on time. Timeliness and preparation are essential-this role requires punctuality and readiness for meetings. The position is onsite 3 days a week.
Key Responsibilities:
- Conduct hands-on usability studies, documenting findings in detailed Word reports.
- Author risk analysis documents as part of the human factors and usability process.
- Proactively follow up and communicate effectively with cross-functional teams.
- Develop and maintain schedules, ensuring timely delivery of tasks and projects.
- Attend and contribute to meetings with preparedness and punctuality.
- Lead and manage human factors/usability aspects of new product development.
Qualifications:
- Minimum 8 years of experience in human factors/usability engineering.
- Proven expertise in leading human factors/usability efforts in new product development.
- In-depth knowledge of Human Factors Engineering principles.
- Prior experience developing regulated medical devices, including conducting human factors analyses and designing and executing formative and summative human factors usability studies.
- Familiarity with relevant quality regulations (21 CFR Part 820.30), human factors/usability engineering standards (IEC 62366-1, ANSI HE75, ISO 14971), and FDA guidance.
Demonstrated success in interdisciplinary collaboration with R&D, Quality, Regulatory, Marketing, and other functions.
Best Regards
Piyush Kumar
Technical Recruiter
Stellent IT
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