Human Factors Engineer (Medical Device Development) Engineering - West Haven, CT at Geebo

Human Factors Engineer (Medical Device Development)

Experience in commercializing medical devices and/or combination products.
In-depth knowledge of regulatory and compliance requirements concerning device risk management and human factors/usability engineering in combination products.
Proven experience in phase-based design control activities, integrated risk management deliverables, and human factors/usability engineering studies across the product development lifecycle.
Demonstrated ability in facilitating interactions between pharmaceutical companies, medical device vendors, and HF consulting firms.
Strong communication, collaboration, and team-building skills.
Proficiency in writing reports, project summaries, and internal/external presentations.
Deep understanding of human factor/usability engineering, safety, performance, and regulatory compliance standards (EU and FDA) for medical devices and combination products.
For office-based positions:
Ability to perform typical office-based tasks including computer usage, communication via various mediums, problem-solving, and collaboration within standard business hours.
Human Factors Engineer (Medical Device Development) Recommended Skills Ergonomics Medical Material Presentations Problem Solving Product Design Risk Management Estimated Salary: $20 to $28 per hour based on qualifications.

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