PROCESSING APPLICATION
Hold tight! We’re comparing your resume to the job requirements…

ARE YOU SURE YOU WANT TO APPLY TO THIS JOB?
Based on your Resume, it doesn't look like you meet the requirements from the employer. You can still apply if you think you’re a fit.
Job Requirements of Human Factor Engineer-Application Re-engineering:
-
Employment Type:
Full-Time
-
Location:
Milpitas, CA (Onsite)
Do you meet the requirements for this job?
Human Factor Engineer-Application Re-engineering
Job Title Human Factors Engineer
Relevant Experience
(in Yrs) 6+ years
Technical/Functional Skills
•Ability to lead usability engineering activities (i.e. establishing usability requirements; creating usability risk analyses, study protocols, and study reports) for a complex, software-controlled electro-mechanical medical device.
•Ability to collaborate with and across various groups and levels of management within the organization, including other engineering groups, marketing, clinical applications, and regulatory.
•Good understanding of FDA Quality System Regulation, ISO 13485 (Quality System) requirements, ISO 14971 (Risk Management) requirements, and Medical Device Directives (MDD) requirements, IEC 62304 Medical Device Software - Software Lifecycle Processes, General Principles of Software Validation - FDA Guidance, and IEC 62366 Medical Devices - Application of Usability
Experience Required
•Minimum 5 years of experience in design or evaluation of user interfaces, Usability engineering, or equivalents.
•Experienced with all phases of the product development life cycle including feasibility, planning, requirements, design and development, V&V, and design transfer.
Roles & Responsibilities
•Responsible for: usability specifications, task analyses, usability risk analyses, and UI evaluation plans for products in collaboration with SW/HW engineers, clinicians, and product managers.
•Strategize, design and execute usability studies at various stages of product development from early prototypes through formative and summative evaluations.
•Author usability study protocols and reports, moderate studies, and analyze study data.
•Advise regulatory, Quality, and R&D teams regarding compliance with IEC 62366, FDA Human Factors Engineering Guidance, and HE75 guidance
•Manage and drive company SOP's /policies/ procedure for alignment with human factors engineering standards and guidance documents
Generic Managerial Skills
•Must have strong organizational, analytical and problem-solving skills
•Must have keen time management skills
•Ability to work in a team proactively, flexibly in an environment
Education
•B.S. degree in Human Factors Engineering, or Industrial Design
Recommended Skills
- Analytical
- Clinical Works
- Ergonomics
- Functional Skills Qualification
- Iec 62304
- Iso 13485
Help us improve Sologig by providing feedback about this job: Report this job
Job ID: U-119662733115
Sologig TIP
For your privacy and protection, when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more.
By applying to a job using Sologig you are agreeing to comply with and be subject to the Sologig Terms and Conditions for use of our website. To use our website, you must agree with the Terms and Conditions and both meet and comply with their provisions.