Job Details

We are seeking experienced Electrical Engineers to support an integration-focused medical device engineering initiative. This role involves working with existing and legacy product designs to align them with internal engineering standards, compliance requirements, and documentation processes.This is an excellent opportunity for engineers with strong experience in design remediation, validation, testing, and regulated product environments.Key ResponsibilitiesSupport design remediation and integration activities for existing productsIdentify and address compliance gaps against internal engineering standards and SOPsParticipate in testing, validation, and design verification activitiesContribute to risk management processes including FMEA and hazard analysisDevelop and maintain detailed engineering documentation and technical reportsCollaborate with cross-functional teams, suppliers, and quality/regulatory stakeholdersAnalyze technical data and provide engineering recommendationsAssist with troubleshooting, fixture development, and test method improvementsRequired QualificationsBachelor's Degree in Electrical Engineering or related discipline4+ years of relevant engineering experience (2+ years with Master's Degree)Experience working in regulated environments, preferably medical devicesStrong background in electrical design documentation and engineering change activitiesHands-on experience with testing, validation, and design verificationFamiliarity with design controls, risk management, and FMEA processesAbility to work with existing/legacy product designsStrong communication and documentation skillsAbility to work onsite full-time in Irvine, CAPreferred SkillsExperience with tools such as Altium Designer, LTspice, or similar platformsKnowledge of troubleshooting methodologies and fixture/test setup developmentExperience supporting compliance alignment and product refinement initiatives