Intern – Manufacturing Electronics / Software Engineering
Core
Support daily manufacturing operations, troubleshooting, and continuous improvement for medical device electronics and software systems.
Role type
Intern – Manufacturing Electronics / Software Engineering
Builds
Medical device components and systems
Domain
Medical device manufacturing / Electronics / Embedded Systems
Deliverable
production ML models | product features | dashboards & analysis | client delivery | infrastructure | physical/clinical work
Required skills
Electronics assembly, embedded systems, software development, sensor technology, test systems, electromechanical product support, circuit board components, troubleshooting basics, programming concepts, software debugging, root cause analysis, data analysis, engineering documentation, design controls, software development lifecycle
Preferred skills
C programming, FPGA, VHDL, CAD, scripting, data analysis tools, Microsoft Office
Technologies
Excel, Minitab, C, FPGA, VHDL, CAD
Responsibilities
Assist with sustaining daily MPS operations across electronics, electromechanical, software, and service-related systems; Support troubleshooting and root cause investigations for production issues, field returns, test failures, software anomalies, or process performance concerns; Contribute to test fixture support, test method improvements, calibration activities, software/firmware checks, and protocol execution; Assist with engineering change order (ECO) documentation, verification activities, implementation support, and post-change effectiveness checks; Help draft or revise work instructions, technical reports, software or equipment documentation, validation evidence, and engineering records; Perform basic data analysis, yield trending, failure tracking, and report generation; Participate in design, manufacturing, or software review activities and provide feedback on manufacturability, serviceability, reliability, usability, and testability; Support continuous improvement projects focused on reducing waste, improving reliability, strengthening test coverage, or improving throughput; Support tasks requiring ESD safety, cleanroom entry, controlled documentation, and regulated manufacturing practices; Gain working knowledge of applicable quality system, risk management, validation, and software lifecycle expectations used in medical device manufacturing.