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Sr. Electrical Engineer

Glaukos Corporation
United States, Massachusetts, Burlington
30 North Avenue (Show on map)
Feb 18, 2026
How will you make an impact?

The Senior Electrical Engineer will play a critical role in advancing Glaukos' nextgeneration corneal crosslinking systems by designing and developing complex electrooptomechanical subsystems used in regulated medical devices.

This role serves as a technical owner for electrical architecture, schematic design, PCB development, and system integration from concept through sustaining engineering. The Senior Electrical Engineer partners closely with mechanical, software, firmware, quality, manufacturing, and regulatory teams to ensure safe, effective, and compliant products that deliver sightsaving technologies to patients.

Success in this role requires deep technical expertise, handson problem solving, and the ability to navigate complex design challenges within a qualitymanaged, FDAregulated environment.

What will you do?

Specific responsibilities include but are not limited to:



  • Design and develop analog, digital, mixedsignal, and power electronic circuits for complex medical device systems.
  • Own schematic capture, multilayer PCB layout, and board bringup testing using Altium Designer.
  • Perform advanced circuit simulations, including DC, AC, transient, Monte Carlo, noise, signal integrity, power integrity, and EMC/EMI modeling.
  • Conduct worstcase, tolerance, reliability, and thermal analyses to ensure longterm product robustness.
  • Drive power distribution and thermal modeling to inform PCB layout strategies and system architecture decisions.
  • Support selection, evaluation, and integration of offtheshelf components such as displays, power supplies, motors, sensors, and singleboard computers.
  • Develop and maintain detailed electrical schematics, wiring diagrams, and documentation aligned with systemlevel architecture.
  • Manage PCB CAD tools, templates, design rules, and component libraries to ensure configuration control and design traceability.
  • Support prototype builds, board bringup, debugging, and rootcause analysis of hardware issues.
  • Design and document PCBA and assembly test fixtures to support development and verification testing.
  • Collaborate closely with software and firmware teams to ensure successful hardwaresoftware integration.
  • Support systemlevel integration and troubleshooting across electrical, mechanical, and software domains.
  • Define, document, and execute electrical design verification and validation protocols in accordance with FDA design controls.
  • Generate and maintain technical documentation, test reports, and design justifications within the Quality Management System (QMS).
  • Support sustaining engineering activities, including ECO implementation, component obsolescence management, and CAPA investigations.
  • Provide technical support to manufacturing, suppliers, and field teams.
  • Support compliance activities related to electrical safety and EMC testing, including IEC 606011 and IEC 6060112.
  • Consistently demonstrate uncompromised ethics and integrity while working within regulatory and quality requirements.

How will you get here?

  • Bachelor's or Master's degree in Electrical Engineering or a related field.
  • 5+ years of progressive electrical engineering experience, including complex PCB and systemlevel design.
  • Strong expertise in analog, digital, mixedsignal, and power electronics.
  • Handson experience with EDA and simulation tools such as Altium Designer (preferred), PSpice, LTspice, MATLAB/Simulink, Allegro PCB, or OrCAD.
  • Proven experience with signal integrity, power integrity, EMC/EMI, and thermal analysis.
  • Experience designing motor control circuits, sensors, and communication interfaces including I2C, SPI, UART, CAN, WiFi, and BLE.
  • Demonstrated experience executing design verification and validation under FDA design control requirements.
  • Working experience within a QMS / ISO 13485 environment.
  • Familiarity with IEC 606011, IEC 6060112, and other applicable medical device standards.
  • Strong analytical, problemsolving, communication, and crossfunctional collaboration skills.
  • Ability to manage multiple priorities and deliver results with minimal supervision.

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