Zing Recruiting
Overview
We are seeking an
R&D Engineer with expertise in Usability and Human Factors
to play a pivotal role in the design and development of medical devices. In this role, you will directly influence how life-changing technologies are designed, tested, and experienced by patients and clinicians. By collaborating closely with design teams, leading usability testing initiatives, and producing regulatory documentation, you will help ensure products are not only compliant, but truly safe, intuitive, and effective. Responsibilities
Serve as a subject matter expert on Human Factors and Usability in medical devices, with in-depth knowledge of IEC usability standards, AAMI Human Factors standards, and FDA Human Factors guidelines. Prepare design control documentation, including Usability Engineering Files (UEF), Use Specifications, Task Analysis, and uFMEA. Lead the planning, development, and execution of usability testing to ensure optimal product performance and safety. Provide training, coaching, and guidance to internal teams on integrating usability design controls into product development processes. Influence usability policies and best practices across the global organization to align with evolving industry standards. Partner with R&D engineers to conduct field research, case study observations, and translate insights into interface requirements, concept selection, and usability validation. Work both independently with minimal supervision and collaboratively within cross-functional teams. Maintain effective communication with global teams at various organizational levels. Ensure compliance with safety regulations and company quality standards. Regular and punctual attendance required. Qualifications
Bachelor’s degree in Engineering or a related field (preferred: Human Factors, Mechanical, Biomedical, Design, or similar). 5+ years of experience in Usability and Human Factors within medical device development. Proven experience conducting formative and summative studies required. Strong expertise in user and use environment research, scenario development, and documentation. Demonstrated ability to conduct and lead usability evaluations, including facilitation, observation, and risk management. Strong problem-solving skills with the ability to analyze complex issues effectively. In-depth knowledge of FDA 21CFR820, ISO 13485, IEC 62366-1, FDA Human Factors Guidance, and ISO 14971. Must be local to Indiana or willing to relocate What We Offer
Direct Hire opportunity Competitive salary: $100,000–$110,000+/year Full benefits package including health, dental, vision, and retirement programs Professional development opportunities, including training, certification support, and conference participation Flexible work arrangements to balance lab and office needs (hybrid potential) The chance to shape global usability strategy and influence the next generation of medical device design Why Join Us?
This role is more than compliance—it’s about championing human-centered design and ensuring patient safety is at the forefront of every product we create. You’ll have the opportunity to collaborate with a passionate, mission-driven team, gain visibility with leadership, and make a measurable impact on how medical devices are experienced worldwide. If you are passionate about advancing usability and human factors engineering, we encourage you to apply! Qualified applicants will be contacted after resume review. Zing Recruiting, a leader in the staffing industry for the past 33 years, continues our vision of ‘linking’ communities through employment. Zing’s dedication to the safety, health & well-being of our associates, clients and communities remains to be a #1 priority. Zing Recruiting is proud to be an EEOE, M/F/D/V, and we are committed to diversity both in practice and spirit at all levels of the organization. We encourage individuals with disabilities to apply for positions and will work to provide accommodation to those who need it. #ZINGMW
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We are seeking an
R&D Engineer with expertise in Usability and Human Factors
to play a pivotal role in the design and development of medical devices. In this role, you will directly influence how life-changing technologies are designed, tested, and experienced by patients and clinicians. By collaborating closely with design teams, leading usability testing initiatives, and producing regulatory documentation, you will help ensure products are not only compliant, but truly safe, intuitive, and effective. Responsibilities
Serve as a subject matter expert on Human Factors and Usability in medical devices, with in-depth knowledge of IEC usability standards, AAMI Human Factors standards, and FDA Human Factors guidelines. Prepare design control documentation, including Usability Engineering Files (UEF), Use Specifications, Task Analysis, and uFMEA. Lead the planning, development, and execution of usability testing to ensure optimal product performance and safety. Provide training, coaching, and guidance to internal teams on integrating usability design controls into product development processes. Influence usability policies and best practices across the global organization to align with evolving industry standards. Partner with R&D engineers to conduct field research, case study observations, and translate insights into interface requirements, concept selection, and usability validation. Work both independently with minimal supervision and collaboratively within cross-functional teams. Maintain effective communication with global teams at various organizational levels. Ensure compliance with safety regulations and company quality standards. Regular and punctual attendance required. Qualifications
Bachelor’s degree in Engineering or a related field (preferred: Human Factors, Mechanical, Biomedical, Design, or similar). 5+ years of experience in Usability and Human Factors within medical device development. Proven experience conducting formative and summative studies required. Strong expertise in user and use environment research, scenario development, and documentation. Demonstrated ability to conduct and lead usability evaluations, including facilitation, observation, and risk management. Strong problem-solving skills with the ability to analyze complex issues effectively. In-depth knowledge of FDA 21CFR820, ISO 13485, IEC 62366-1, FDA Human Factors Guidance, and ISO 14971. Must be local to Indiana or willing to relocate What We Offer
Direct Hire opportunity Competitive salary: $100,000–$110,000+/year Full benefits package including health, dental, vision, and retirement programs Professional development opportunities, including training, certification support, and conference participation Flexible work arrangements to balance lab and office needs (hybrid potential) The chance to shape global usability strategy and influence the next generation of medical device design Why Join Us?
This role is more than compliance—it’s about championing human-centered design and ensuring patient safety is at the forefront of every product we create. You’ll have the opportunity to collaborate with a passionate, mission-driven team, gain visibility with leadership, and make a measurable impact on how medical devices are experienced worldwide. If you are passionate about advancing usability and human factors engineering, we encourage you to apply! Qualified applicants will be contacted after resume review. Zing Recruiting, a leader in the staffing industry for the past 33 years, continues our vision of ‘linking’ communities through employment. Zing’s dedication to the safety, health & well-being of our associates, clients and communities remains to be a #1 priority. Zing Recruiting is proud to be an EEOE, M/F/D/V, and we are committed to diversity both in practice and spirit at all levels of the organization. We encourage individuals with disabilities to apply for positions and will work to provide accommodation to those who need it. #ZINGMW
#J-18808-Ljbffr