Electrical Engineer

This is a remote position. We are seeking a highly skilled and detail-orientedElectrical Engineerto support the design, testing, and validation of electrical components foractive implantable medical devicesand related hardware systems. The ideal candidate will have hands-on experience inproduct development, particularly throughdesign verification testing (DVT)and the transition intoproduction-scale manufacturing. This role requires strong analytical skills, technical leadership, and the ability to collaborate with cross-functional teams in a regulated environment. Key Responsibilities • Lead and executeelectrical design verification testing (DVT)activities for implantable and external medical devices. • Develop and documenttest protocols, test plans, and verification proceduresin compliance with quality and regulatory standards. • Performbench testingusing standard electrical engineering laboratory equipment (oscilloscopes, multimeters, function generators, etc.). • Analyze and interpret test data; summarize findings and provide clear technical documentation. • Coordinate and tracktest investigations, ensuring timely completion and documentation accuracy. • Lead or supportfailure analysis and root cause investigationsfor test nonconformances and component issues. • Work closely withR&D, Quality, Manufacturing, and Systems Engineeringteams to resolve technical challenges and ensure design robustness. • Supportyield improvement activities, identifying and implementing process or design enhancements. • Maintain strict adherence todesign control and quality system requirements, ensuring full traceability and compliance withFDA, ISO 13485, and IEC standards. Must-Have Qualifications • Bachelor’s degree in Electrical Engineeringor related disciplinewith professional experience inelectrical engineering inmedical device product developmentor a highly regulated industry. • Proven experience in theDVT phaseof product development and transition to manufacturing. • Strong background indata analysisusingMinitab, JMP, or Microsoft Excel. • Demonstrated ability to lead and close projects involvingcross-functional collaboration. • Experience performingbench-level testing and troubleshootingusing standard EE test instruments. • Excellenttechnical documentation, communication, and problem-solvingskills. • Proven ability to manage multiple priorities while maintaining attention to detail and compliance. Preferred Qualifications • Experience withactive implantable or Class III medical devices. • Knowledge ofIEC 60601,ISO 14708, andFDA Design Control (21 CFR 820.30)standards. • Familiarity withSPICE simulation tools,PCB design and layout, orcircuit debugging. • Experience withroot cause analysis, FMEA, and CAPA methodologies. • Demonstrated success inyield improvement initiativesand process optimization. This is intended for inclusion in Pharmavise’s talent database to build a qualified pool of professionals for future medical device client requisitions. Originally posted on Himalayas