- Support test design and execution including calibration, characterization, and engineering testing in coordination with various technical system teams. - Lead and complete system/subsystem-level robotic integration across multi-functional subject areas. - Identify root cause and resolve novel issues that arise across the R&D systems by working cross-functionally with mechanical, electrical, software, robotic controls, and clinical teams. - Characterize and de-risk the design from prototype to subsystem level. - Analyze test results and provide meaningful insights and conclusions. Implement, evaluate, and demonstrate hardware and software proof of concept. - Drive continuous improvement in integration activities and processes such as testing, calibration, issue handling, system upgrades and feature rollout, design feedback, etc. - Support development of test methods and fixtures for system/subsystem integration, test, calibration, and transfer to manufacturing.- Support clinical and human factors teams to test new features in simulation and implement in labs. - Serve as technical expert for setting up, operating, maintaining, and debugging the system in clinical labs. - Document and resolve issues in clinical lab setting. - Troubleshoot and repair issues that commonly arise across the R&D system fleet. - Work with software engineers to understand and modify existing code. - Work with mechanical or electrical engineers to upgrade hardware components. - Maintain the configuration and records of all systems used for development and verification.

Ensured protocol compliance and data integrity in clinical trials for an implantable neurostimulator.Documented detailed visit and follow-up reports on over thirty research participants across various clinics in the northeastern United States for over two years.Developed and executed product risk assessment, usability verification, and engineering validation plans.Project Lead for Electromagnetic Compatibility and ISO 60601 Medical Safety Testing.Project Manager in the implementation of a standardized kit used for controlled transportation of medical electrical equipment. Designed and standardized a more efficient internal auditing framework for system compliance across the company using ISO and US CFR standards. Prepared official documentation for FDA Pre-Market Approval Submissions. Coordinated communication between research clinics, third-party companies, and independent physicians in the clinical testing and operations of the company products.

Constructed custom-built controller boards and chargers for robotic prostheses. Tested and analyzed circuits. Prepared testing protocols, test reports, and other regulatory documents pertaining to manufacturing and production when needed. Documented incoming inspections of stock materials and created shipments for outgoing products.