OverviewOur client in Limerick is seeking an experienced Human Factors Engineer to join their European hub for R&D and innovation. As they develop Class I to Class III medical devices, you will work across disciplines to support bringing ideas from concept to market under high standards of quality, regulatory compliance and patient safety. You will be responsible for integrating human-centered design principles into the product development lifecycle. You will reduce user-related errors and support the development of safe medical devices through careful design validation and documentation.Requirements5 - 7 years' experience in usability engineering ideally medical device / pharma (syringe preferably)Experience in gathering HF data and feeding that into design team as design inputs.Risk documentation experience (dfmea, ufmea, design inputs table, DHF document general experience)Experience in application of IEC 62366 standard for medical device developmentExperience in setting up, conducting, and concluding (data analysis) a usability trials.Strong analytical and problem-solving skills.Excellent communication and collaboration skills.Proficiency in experimental design and user research methodologies.Ability to analyse human behaviour and performance.Familiarity with user-centered design principles.BenefitsCompetitive and attractive employee compensation packagePension contributionsHealth insurancePaid public holidays.LocationLimerick, Ireland | hybridDetailsSeniority level: Entry levelEmployment type: Full-timeJob function: ManufacturingIndustries: Medical Equipment ManufacturingHow to applyDirect message the job poster from Oxford Global Resources. Sign in to set job alerts for “Usability Engineer” roles.
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