Sr. Systems Engineer

Biomedical Search

  • Billerica, MA
  • 23 days ago
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    Skills

    • Biomedical Engineeringunmatched
    • Biomedical Softwareunmatched
    • Cardiac Monitoringunmatched
    • Catheterizationunmatched
    • Communication Skillsunmatched
    • Cross-Functionalunmatched
    • Electricityunmatched
    • Electrocardiogramunmatched
    • FDA (Food and Drug Administration)unmatched
    • ISO (International Organization for Standardization)unmatched
    • International Electro-Technical Commission (IEC)unmatched
    • Leadershipunmatched
    • Manufacturing Requirementsunmatched
    • Medical Equipmentunmatched
    • Medical Productsunmatched
    • Medical Protocolsunmatched
    • Patient Careunmatched
    • Performance Managementunmatched
    • Problem Solving Skillsunmatched
    • Process Improvementunmatched
    • Product Designunmatched
    • Product Developmentunmatched
    • Regulatory Submissionsunmatched
    • Risk Managementunmatched
    • Software Engineeringunmatched
    • Startupunmatched
    • Strategic Planningunmatched
    • Systems Engineeringunmatched
    • Team Playerunmatched
    • Technical Leadershipunmatched
    • Technical Supportunmatched
    • Technical Writingunmatched
    • Test Strategyunmatched
    • Validation Testingunmatched

    Description

    Position Overview

    Join a growing medical device company developing innovative vascular technologies that improve patient care. We are seeking a Senior Systems Engineer to lead product development from concept through commercialization, driving system design, design controls, risk management, and verification & validation (V&V) in a collaborative, cross-functional environment.

    Key Responsibilities

    • Lead system design and product development activities from concept through commercialization.
    • Own design controls, risk management, and system-level V&V.
    • Develop test strategies, protocols, reports, and technical documentation to support regulatory submissions.
    • Provide technical leadership to internal teams and external engineering partners.
    • Collaborate with Engineering, Quality, Regulatory, Manufacturing, and Clinical teams.
    • Drive improvements in product performance, reliability, and manufacturability.

    Qualifications

    • Bachelor's degree in Mechanical, Electrical, Biomedical, Software Engineering, or a related field (Master's preferred).
    • 7+ years of medical device product development experience in an FDA-regulated environment.
    • Strong expertise in design controls, risk management, and verification & validation.
    • Experience working across mechanical, electrical, and software systems.
    • Excellent leadership, communication, and problem-solving skills.

    Preferred Qualifications

    • Startup or early-stage medical device experience.
    • Experience with cardiac monitoring, ECG, electrophysiology, or catheter-based technologies.
    • Knowledge of FDA Design Controls, ISO 14971, IEC 60601, and other applicable medical device standards.

    Numbers & Facts

    LocationBillerica, MA

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