Human Factors Engineer

Lead Human Factors EngineerLead Human Factors Engineer possessing deep expertise in human factors engineering, usability engineering, and user-centered design to support and lead the development of safe, effective, and intuitive medical devices from concept through commercialization.Essential Duties and Responsibilities:The incumbent may be asked to perform other function-related activities in addition to the below mentioned as responsibilities as reasonably required by business needs.This position is responsible for performing the following tasks while driving execution of human factors work aligned with program and organizational objectives:Expert in FDA Human Factors guidance, IEC 62366-1/-2, ANSI/AAMI HE75, and ISO 14971 use-related risk managementOwns usability engineering strategy across the product lifecycleDesigns and executes formative and summative usability studies, including protocols, moderator guides, and root-cause analysis of use errorsConducts user research and clinical/customer evaluations of real-world use scenarios and environmentsAnalyzes test results and translates findings into defensible design and risk conclusionsAuthors and reviews UI/UX specifications, labeling, and IFUs as risk controlsSME for Design Controls, Design Validation, and quality risk management within a regulated QMS; complies with all applicable FDA and ISO requirementsIndependently authors protocols, reports, and requirements; relied upon for thorough review of documentation, including department proceduresLeads usability work cross-functionally across R&D, software, quality, regulatory, clinical, and marketingMentors junior staff and drives results in highly complex projectsSupervisory Responsibilities:Provide technical leadership and mentoring to engineers and product development teamsQualificationsEducation:Bachelor's or Master's degree in Usability/Human Factors Engineering, Mechanical Engineering, Biomedical Engineering, Systems Engineering or related field. Advanced degree preferred.Experience:8+ years of Human Factors/Usability Engineering experience, with the majority in the medical device industry, required with a Bachelor's Degree6+ years of Human Factors/Usability Engineering experience, with the majority in the medical device industry, required with a Master's DegreeSkills:Expert knowledge of FDA Human Factors guidance, IEC 62366-1/-2, ANSI/AAMI HE75, and ISO 14971Depth in Design Controls, Design Validation, and quality risk management within a regulated QMSAbility to define and own usability engineering strategy across the product lifecycleExpertise in use-related risk analysis — task analysis, critical tasks, use errors, and usability failure modesExpertise performing research on user interfaces such as physical devices, complex systems, and GUIs.Hands-on experience running formative and summative usability studies, from protocol to root-cause analysisSkilled in user research and clinical/customer evaluations of real-world use scenariosSkilled in root cause analysisSkilled in user requirement developmentSkilled in critical task analysisSkilled in regulatory submission supportStrong analytical skills; translates test results into defensible design and risk conclusionsExperience authoring UI/UX specifications, labeling, and IFUs as risk controlsExcellent technical writing; produces audit-ready documentation and critically reviews proceduresProven cross-functional leadership, mentorship, and drive for results on highly complex projectsPhysical Demands:The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.The employee is regularly required to sit, stand, walk, and reach with hands and arms, use hands to finger, handle, feel, and be able to talk and hear.Specific vision abilities required by this job include close vision, color vision, and the ability to adjust focus.Ability to lift or move up to 25 pounds.Ability to work flexible hours.Work Environment:This position follows a hybrid work model, requiring the employee to be on-site at our Louisville, CO location at least 4 days per week, with the flexibility to choose which day to work remote.Travel:Ability to travel up to 10% as needed.So why join Hologic?We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. We offer a competitive salary and annual bonus scheme, one of our talent partners can discuss this in more detail with you.If you have the right skills and experience and want to join our team, apply today. We can't wait to hear from you!The annualized base salary range for this role is $128,200 - $200,500 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.Agency and Third-Party Recruiter Notice: Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.As part of our commitment to a fair and accurate evaluation of each candidate's qualifications, we require all applicants to refrain from using AI tools, such as generative AI or automated writing assistance, during any stage of the interview process. Responses influenced by AI may result in disqualification. We appreciate your understanding and cooperation in ensuring a transparent and equitable selection process.Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.