Senior Systems Engineer

Company Overview Embark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. At PROCEPT, we put the patient first in everything we do and are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as prostate gland enlargement) through innovation in surgical robotics. As our company succeeds and grows, we improve the quality of life of patients, provide more effective treatment options for surgeons, uphold the trust of our shareholders. That starts with a commitment to our People with a focus on creating an evolving landscape for your career, brimming with transformative opportunities that provide continuous career growth opportunities.

The Opportunity That Awaits You

At PROCEPT BioRobotics, we don’t just build machines, we build precision robotic technology that restores quality of life for men with BPH. We are seeking an experienced Senior Systems Engineer to lead system-level engineering activities for our next-generation medical robotic platform. This individual will play a critical role in requirements development, verification & validation (V&V), and ensuring complete system-level test coverage in a regulated medical device environment.

What Your Day-To-Day Will Involve

Own and drive system-level verification and validation (V&V) activities Develop, review, and refine system requirements to ensure clarity, testability, and traceability Design and execute system-level test protocols, including integration, functional, performance, and reliability testing Lead development of automated test methods and automated test cases to improve repeatability, efficiency, and regression coverage. Develop test fixtures as needed Ensure proper linkage between requirements, risk controls, and verification activities Identify coverage gaps and ensure proper verification of all functional, performance, safety, and risk-control requirements Collaborate cross-functionally with hardware, software, mechanical, and clinical teams Support regulatory submissions and audits with complete, well-structured V&V documentation Contribute to continuous improvement of systems engineering and test processes

The Qualifications We Need You to Possess Bachelor’s or Master’s degree in Electrical Engineering, Mechanical Engineering, Biomedical Engineering, or related field 5+ years of experience in systems engineering within a regulated medical device environment Strong experience in system-level testing and V&V Demonstrated experience writing and refining clear, testable requirements Hands-on experience developing automated test methods and automated test cases Experience with scripting or programming languages used for test automation (e.g., Python, MATLAB, C++, LabVIEW, or similar) Experience building and maintaining traceability matrices Familiarity with risk management processes (e.g., ISO 14971)

Preferred Qualifications

Experience with ISO 8600 standards for medical electrical equipment Experience in medical robotics or complex electromechanical systems Experience with system-level automated test frameworks Experience supporting FDA submissions or notified body audits