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Lawrence, Massachusetts, USAPermanent positionFull time

Staff Human Factors Engineer

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PURPOSE AND SCOPE:

Acts as a subject matter expert to support the development of products by working collaboratively with interdisciplinary teams to plan, direct, and (where applicable) perform human factors/usability engineering activities. Serve as a leader in the design and evaluation of processes, products, and systems with respect to human factors/usability considerations (i.e. how intended users interact with systems given their goals, tasks, and environment).

PRINCIPAL DUTIES AND RESPONSIBILITIES:

  • Technically proficient subject matter expert and technical leader in human factors engineering responsible for lifecycle application of human factors design process, principles, analysis, and usability testing methods
  • Develops collaborative working relationships with a range of functions including, but not limited to R&D, Marketing, Quality,  Regulatory and Clinical functions
  • Provides technical guidance and/or design expertise to a wide variety of contexts including, but not limited to:
    • Directing R&D, Clinical, Marketing, and other staff regarding human factors considerations
    • Directing the definition and development of system user interface design(s)
    • Supporting the definition and development of labeling and training
  • Contributes to user interface designs by providing guidance, ideas, and review to UX designers and developers.
  • Collaborates with peers and other staff on human factors processes and principles
  • Ensures that development plans, processes and activities address human factors engineering process and design requirements in order to maximize product usability and use-related safety.
  • Identifies user needs/requirements, and collaborates with product management/marketing  to ensure designs meet the user and customer needs.
  • Collaborates with development teams to optimize designs in consideration of use error risk and overall usability.  Leads and authors the identification, analysis, and evaluation of use-related risk and development of risk controls.
  • Responsible for planning and conducting human factors analyses, unstructured testing, and structured usability studies. This may involve directing others or personally executing study/protocol design, study execution, data collection and analysis, as well as writing study reports and communicating findings and recommendations to teams.
  • Contributes to the design development process by participating in design review meetings, reviewing and contributing to design inputs, risk analysis, and reviewing and testing new product performance.
  • Applies persuasion to change the thinking of and/or gain acceptance from others in sensitive situations while maintaining an effective working relationship.
  • Oversees the monitoring, completion and accuracy of documents produced by human factors engineering activities.
  • Responsible for HF assessments included in regulatory documents submitted to the FDA (or other regulatory bodies).
  • Responsible for ensuring compliance to applicable standards and guidance.
  • Contributes to human factors process development and improvements and development of associated templates.
  • Responsible for keeping current on new developments in human factors engineering.
  • Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise.  
  • Normally receives little instruction on day-to-day work, general instructions on new assignments.
  • May provide assistance to lower-level staff with more complex tasks that require a higher level of understanding of functions.
  • May escalate issues to supervisor/manager for resolution, as deemed necessary.
  • Mentors other staff as applicable.
  • Reviews and complies with the Code of Business Conduct and all applicable company policies and procedures, local, state, and federal laws and regulations.
  • Assists with various projects as assigned by a direct supervisor.
  • Other duties as assigned.

Additional responsibilities may include focus on one or more departments or locations.  See applicable addendum for department or location specific functions.

PHYSICAL DEMANDS AND WORKING CONDITIONS:

  • The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Approximately up to 20-25% travel is expected of this position.

SUPERVISION:

None, although will typically serve as a lead for human factors engineering on project cross-functional teams.

EDUCATION:

  • Bachelor’s Degree required; Advanced Degree preferred
  • Degree in Human Factors Engineering, Industrial Engineering, Human-Computer Interaction, Cognitive Psychology, or related field with relevant work experience demonstrating acquisition and application of position-relevant skills.

EXPERIENCE AND REQUIRED SKILLS:

  • Minimum 9+ years of human factors/usability experience required.
  • Demonstrated experience leading human factors/usability in new product development.
  • Strong interpersonal skills with the ability to communicate with all levels of management with diplomacy and tact.
  • Ability to work independently with minimal supervision
  • Ability to address issues and solutions in clear and concise written and verbal communication
  • Comprehensive knowledge of Human Factors Engineering
  • Prior experience developing regulated medical devices, including performing 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
  • Track record of interdisciplinary collaboration with R&D, Quality, Regulatory, Marketing and other functions.

EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity

Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.

Career with a purpose

Career with a purpose

We offer an opportunity to create and deliver treatments that save and change lives for the better. We’ll support your ongoing development. And you’ll be part of a dedicated team of people who inspire each other to create the best possible healthcare outcomes each and every day.
Inclusion and diversity

Inclusion and diversity

Joining Fresenius Medical Care means becoming part of a team that values diversity. We embrace the wealth of different backgrounds, cultures, experiences and opinions that make up our workforce and strive to create an inclusive atmosphere in which all our employees feel valued.
Stability

Stability

Developing innovative products and continuously improving our renal therapies made us the clear market leader in the production of hemodialysis machines, with sustainable, profitable growth . This position provides our 125000 employees with the stability and security they need to help improve the lives of our patients.
Learning and development

Learning and development

We offer participation in programs at world-class business schools, leadership development, regular training for our nurses, health care professionals and manufacturing staff and digital access to high-quality educational content for all employees worldwide 24/7. 
Local benefits

Local benefits

Our employees enjoy both local and global opportunities for growth and personal fulfilment. We offer local benefits designed to suit the requirements of the respective country and place of work to create ideal conditions everywhere.
Work-life balance

Work-life balance

We want to empower people to deliver better care. Therefore, we promote a better work-life balance through flexible working hours, part-time models, the possibility to work from home, and more.
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At a glance

Earliest possible start:

As from now

Contract type:

Permanent position

Company:

Fresenius Medical Care

Region / Business Unit:

North America

Location:

Lawrence, Massachusetts, USA

Working condition:

Full time

Job function:

Research and DevelopmentProduct Development and Engineering

Reference number:

R0136790

Publishing Date:

01/19/2024

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Develop new, tailored solutions for dialysis patients

About 3.5 million patients worldwide depend on regular dialysis treatment. Fresenius Medical Care is committed to enabling a future worth living for these people. Our teams in Research and Development, operating in 23 locations across three regions, are responsible for the ongoing development of the medical products and treatments required across the renal care spectrum.

We drive research on innovative dialysis devices and turn it into reality. To deliver solutions that are continuously optimized and tailored to meet patients’ specific needs, we develop IoT-supported diagnostic methods and evidence-based, individualized treatments. Our integrated, multidisciplinary approach to research and development speaks to specialists as well as generalists.

Deliver technical excellence on a global scale

Discover the benefits of joining a global organization that is committed to excellence and quality. We support your career journey by helping you fulfill your ambitions. That’s how we create value for our patients and our employees.

As market leader, Fresenius Medical Care sets new, higher standards in dialysis. Help us define them: become part of a talented team that drives innovation in health care. Join our scientists and professionals in delivering excellence on a global scale.

Collaborative

We care about sharing information and experiences as this helps us learn from our mistakes and each other. We tackle challenges together by reaching out to colleagues both near and far. We communicate openly.

Proactive

We challenge the status quo and show interest in what happens around us. We ask questions to clearly understand what needs to be done and take ownership of the results.

Reliable

We live up to our own expectations, show respect and lead by example. We act with integrity and in line with our standards every day.

Excellent

We make things better today than they were yesterday. We pitch ideas on how to improve and innovate.

What we stand for

Empowering people. Advancing care. Inspiring with our purpose and values.

Everything we do here is about making people’s lives better, simpler and longer. Our teams work cross-functionally to reproduce the complex function of kidneys with treatments that meet high quality standards, improve clinical outcomes, and are sustainable and compliant. Internally, we promote diversity and inclusion as key elements of a positive, supportive work environment. Our values support our mission to develop high quality products and services, to have a positive impact on the health and wellbeing of patients, and to lead Fresenius Medical Care towards a successful, sustainable future.