This is a remote position.

We are seeking a highly skilled and detail-oriented Electrical Engineer to support the design, testing, and validation of electrical components for active implantable medical devices and related hardware systems. The ideal candidate will have hands-on experience in product development, particularly through design verification testing (DVT) and the transition into production-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 execute electrical design verification testing (DVT) activities for implantable and external medical devices.
Develop and document test protocols, test plans, and verification procedures in compliance with quality and regulatory standards.
Perform bench testing using standard electrical engineering laboratory equipment (oscilloscopes, multimeters, function generators, etc.).
Analyze and interpret test data; summarize findings and provide clear technical documentation.
Coordinate and track test investigations, ensuring timely completion and documentation accuracy.
Lead or support failure analysis and root cause investigations for test nonconformances and component issues.
Work closely with R&D, Quality, Manufacturing, and Systems Engineering teams to resolve technical challenges and ensure design robustness.
Support yield improvement activities, identifying and implementing process or design enhancements.
Maintain strict adherence to design control and quality system requirements, ensuring full traceability and compliance with FDA, ISO 13485, and IEC standards.

Must-Have Qualifications

Bachelor’s degree in Electrical Engineering or related discipline with professional experience in electrical engineering in medical device product development or a highly regulated industry.
Proven experience in the DVT phase of product development and transition to manufacturing.
Strong background in data analysis using Minitab, JMP, or Microsoft Excel.
Demonstrated ability to lead and close projects involving cross-functional collaboration.
Experience performing bench-level testing and troubleshooting using standard EE test instruments.
Excellent technical documentation, communication, and problem-solving skills.
Proven ability to manage multiple priorities while maintaining attention to detail and compliance.

Preferred Qualifications

Experience with active implantable or Class III medical devices.
Knowledge of IEC 60601, ISO 14708, and FDA Design Control (21 CFR 820.30) standards.
Familiarity with SPICE simulation tools, PCB design and layout, or circuit debugging.
Experience with root cause analysis, FMEA, and CAPA methodologies.
Demonstrated success in yield improvement initiatives and 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.

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