Senior Mechatronics Engineer – Robotic Medical Devices

TekWissen LLC; Newton (MA); On-site; USD 110,000 - 170,000; Full time

Benefits offered by this job

Equal opportunity employer

Job summary

TekWissen Group is seeking a Component Engineer IV for its Endovascular Robotics division in Newton, MA. You will join R&D to advance a next‑gen robotic platform, working hands-on with complex electro‑mechanical assemblies and contributing from prototype to verification builds in a regulated medical device environment.

You will lead troubleshooting, document process improvements, and collaborate across electrical, software, and mechanical teams, ensuring traceability and robust test methods for

Qualifications

• Must have 10+ years in complex electromechanical system R&D environment.
• Degree in Electrical/Mechanical/Mechatronics/Robotics or related field; advanced degree preferred.
• Experience in heavily regulated industries such as medical devices or aerospace.
• Proven hands-on experience in assembly and test of electromechanical systems; CAD proficiency desired.

Responsibilities

• Maintain and upgrade robotic systems for R&D under design control processes.
• Lead system configuration management to ensure traceability for R&D and clinical activities.
• Perform hands-on system troubleshooting with cross-functional teams.
• Develop and release test methods, protocols, and reports via ECOs.
• Support procurement, BOM planning, and future builds; propose process improvements.

Skills

Cross-functional collaboration

Project management

System troubleshooting

Documentation

Education

Bachelor's or Master's in Electrical/Mechanical/Mechatronics/Robotics/Manufacturing Engineering

Associate's degree with exceptional experience

Tools

MATLAB/Simulink

LabVIEW

SolidWorks

PLM/ECOs

MS Office

Job description

TekWissen Group is seeking a Component Engineer IV for its Endovascular Robotics division in Newton, MA. You will join R&D to advance a next‑gen robotic platform, working hands-on with complex electro‑mechanical assemblies and contributing from prototype to verification builds in a regulated medical device environment.

You will lead troubleshooting, document process improvements, and collaborate across electrical, software, and mechanical teams, ensuring traceability and robust test methods for