13 human factors researcher jobs at 10 companies in Everett, MA
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Sr. Human Factors Engineer
St. Paul or Westford or Santa Clara
$78k-$156k/yrOnsiteFull Time
AbbottNYSE: ABT: Manufactures medical devices, diagnostics, and nutritional health products.
Experience in human factors and cognitive psychology for software design, usability research, training, FDA compliance, cross-functional collaboration, and ability to travel ~25%.
AbbottNYSE: ABT: Provides medical devices, diagnostics, and science-based nutritional products.
Bachelor's degree or equivalent experience; experience designing software for complex applications; expertise in human factors and cognitive psychology; strong verbal/written communication; ability to travel ~25%.
Lila Sciences: Develops an AI platform for autonomous scientific research and discovery.
4+ YOERequires 4–8 years in UX research or human factors for complex operational, industrial, or scientific software, plus research methods, high-stakes interface design, Figma prototyping, and cross-functional communication.
Figma, SCADA, Manufacturing Execution System (MES), WCAG 2.2, ISO 9241-210, ANSI/ISA-101
Goddard: Engineering and industrial design firm for medical and robotic products
5+ YOEBachelor's degree and 5+ years HF/usability engineering for medical devices, regulatory standards knowledge, usability testing, prototyping, strong communication and teamwork.
Figma, Adobe XD, Sketch, Axure, SolidWorks CAD, Microsoft, Google
MedtronicNew York Stock Exchange: MDT: Develops and manufactures medical devices and digital health solutions.
4+ YOEBachelor's degree and 4+ years of relevant experience, or an advanced degree and 2+ years. Requires human subjects research, data analysis, medical device design, and FDA/IEC guidelines experience.
MedtronicNYSE: MDT: Developing and manufacturing medical technologies and therapies globally.
4+ YOEBachelor's degree and 4+ years of relevant experience, or advanced degree and 2+ years. Requires human subjects research, data analysis, medical device design, and FDA and IEC guidelines experience.
Human Factors Engineering (HFE) Lead - Associate Engineering Fellow (AEF)
Lexington, Massachusetts, United States
$154k-$243k/yrOnsiteFull Time
TakedaTokyo Stock Exchange / New York Stock Exchange: 4502 / TAK: Researches, develops, and manufactures prescription pharmaceutical medicines.
7+ YOEDoctorate or advanced degree with extensive HFE experience; 7+ years HFE or equivalent, experience with user research, usability studies, risk management, regulatory standards (IEC/ISO), vendor management, and cross-functional collaboration.
Charles River Analytics: Develops human-centered AI and intelligent systems for national security.
PhD student in Computer Science/Human Factors or related field; experience in HCI/UX/human factors; strong verbal and written skills; able to work independently and in teams; U.S. citizenship required.
Rhythm PharmaceuticalsNASDAQ: RYTM: Develops precision medicines for rare neuroendocrine and obesity diseases.
8+ YOE8+ years device or combination-product development experience, bachelor\u0002s in engineering, knowledge of design controls/DHF/risk management/human factors, experience through commercialization, ability to lead cross-functional teams.
Sentec: Provides non-invasive respiratory monitoring and therapy solutions.
3+ YOE3+ years in human factors/usability or regulatory affairs in medical devices; Bachelor's in biomedical engineering or related; strong technical and analytical skills; familiarity with FDA and EU MDR preferred; ability to travel ~5 trips/year.
ClariMed: Human-centered design and regulatory services for medical device development.
Experience in participant recruitment, human factors, clinical or market research, study coordination, or related work; project management, communication, organization, problem-solving, and recruitment strategy skills required.
CRM, participant databases, scheduling platforms, research management software
MerckXETRA: MRK: A science and technology providing healthcare, life science, and electronics solutions.
10+ YOEMaster's in life sciences or equivalent; 10+ years regulatory affairs experience with ≥5 years in digital health/SaMD; experience with IDE/510(k)/PMA, CE marking (EU-MDR), software validation, human factors, ICH/GCP/ISO 14155; FDA/EMA interactions; fluency in English; must be eligible to work in the US.
eSTAR, ISO 13485, MDSAP, ISO 14155, ICH, GCP, EU-MDR, IDE, 510(k), PMA