Job description
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
Who can apply
Eligible countries: United States. Accepted UTC offsets: UTC-10, UTC-9, UTC-8, UTC-7, UTC-6, UTC-5, UTC+14. Review the full description for employer-specific work authorization, residency and schedule requirements.