Principal Human Factors Engineer specialized in Lifesciences (Medical

Benefits

• 401(k)
• 401(k) matching
• Relocation bonus

Job Title: Principal Human Factors Engineer specialized in Lifesciences (Medical Devices)

Location: Fort Worth, TX

Apply user-centered design principles to the

Research, design, and development of Alcon's Digital Health Suite and Surgical Instrumentation

projects.

Apply Human Factors Engineering (HFE) methods and principles to design and develop products

that meet customer technical/functional specifications as well as manufacturing

cost/efficiency requirements.

Accountable to delivering on traditional HFE activities and deliverables such as HFE Plans,

Development of Task Analysis to support Risk management activities, planning and conducting

usability evaluations, cognitive walk-throughs, data analysis to identify opportunities and

control risks,

effectively report on formative and summative evaluation results, and proactively present

recommendations to product teams.

Author Human Factors artifacts required for regulatory compliance,

specifically IEC 62366, AAMI HE75, FDA Applying Human Factors and Usability Engineering to

Medical Devices.

Supportive requirements

This specialized skillset works integrally with product teams to ensure optimal usability

characteristics and use safety of current and future Alcon products.

This position serves to identify, define, analyze, validate and report on Human Factors

Engineering and Usability considerations to ensure they are incorporated in the design process

related to Alcon products.

The position also involves advocacy for end users through the conduct of interviews or surveys

of users or customers to collect information on topics such as use-related requirements, use

risks, needs, user profiles, task analysis and user interfaces.

Additionally, the position involves needs assessment of the user-interface elements and

usability characteristics of both current and future Alcon products, with special emphasis on

aspects related to use safety.

The contracted service is accountable for ensuring user needs and requirements are translated

into design concepts in collaboration with the product design teams.

Maintain awareness of the state-of-the-art methods as applied to life-sciences / medical device

industry.

The contracted service is expected to plan and own their activities including collaborating with

multi-disciplinary teams, including design, engineering, marketing, quality, regulatory, and

clinical areas.

Candidate minimal requirements

Bachelor's Degree or Equivalent years of directly related experience (Assoc.+11 yrs; M.S.+5 yrs;

PhD+4 yrs)

The ability to fluently read, write, understand, and communicate in English.

At least 4 Years of Experience delivering HFE support of medical device (SiMD, SaMD, etc)

development

Must have delivered the full HFE file to support at least one successful medical device FDA

approval and IEC 60601-1-6 certification (IEC 62366 TRF)

Compensation: $90,000.00 - $110,000.00 per year

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