Job Description An employer is seeking a Human Factors Engineer for an opportunity in the Cincinnati, OH area. This HFE will be responsible for collaborating with cross-functional teams (R&D, Regulatory, Quality) to ensure human factors are integrated throughout the product lifecycle, conducting usability evaluations and risk assessments related to labeling and reprocessing, supporting validation activities for labeling, including IFUs, packaging, and device markings. This HFE will be supporting a clinical trial and will be expected to analyze reprocessing workflows to identify usability risks and recommend design improvements as well as documenting findings and contribute to regulatory submissions (e.g., HF reports, validation protocols). Other day to day responsibilities will include participation in design reviews and provide HF input on product changes and new developments. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/. Skills and Requirements 5+ years in a human factor engineering role 5+ years of experience in medical device development 5+ years hands on experience with labeling validation processes Familiarity with reprocessing workflows in MedTech (e.g., cleaning, disinfection, sterilization steps) Experience in sterile reprocessing of medical devices, especially from a human factors perspective (not looking for ex-SPT turned HFE) Additional experience in labeling validation beyond core responsibilities