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ZOLL Medical

Emergency care medical devices and software

Principal Systems Engineer - Medical Devices

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeSan Jose, CA, USAHybrid

About the Job

Requirements

  • An advanced degree in Engineering, including training and experience in systems, electronics, software, and mechanical engineering.
  • At least 15 years of experience developing electronic hardware and embedded software systems or subsystems for complex, real-time measuring instruments.
  • At least 10 years of experience as a Systems Engineer, leading architectural design and systems engineering of complex, real-time medical measuring instruments.
  • At least 7 years of experience leading systems engineering of multiprocessor-based systems incorporating analog/digital electronics and embedded real-time software.
  • Project management experience and training.
  • Extensive knowledge and experience in system-level design and development of multiprocessor-based medical instruments containing biomedical signal acquisition and processing electronics and embedded software systems.
  • Ability to translate high-level product requirements into system- and subsystem-level specifications and designs.
  • Success leading engineering teams in architecture, system-level design, integration, and verification of portable, battery-operated, multiprocessor-based measuring or patient-treatment systems.
  • Working knowledge and experience with low-level analog signal acquisition, digital/microprocessor systems design, power supplies, embedded real-time software development, digital signal processing, real-time operating systems, analog/digital control systems, displays, batteries, data storage, and wireless communications systems.
  • Working knowledge of mechanical engineering issues and processes associated with electronics packaging, small moving mechanisms, molding, and machining processes.
  • Ability to independently analyze and evaluate electronic circuitry, software, and mechanical designs using drawings, schematics, source code, technical education, and experience.
  • Thorough understanding of product development and engineering project management processes.
  • Experience with and sensitivity to human factors issues associated with medical device use.
  • Knowledge and experience developing products under FDA and European Community medical device regulations and standards.
  • Verbal and written communication skills, with demonstrated success in technical decision-making and people management/leadership in a matrix environment.
  • Business acumen.

Responsibilities

  • Work with project and program management to establish and refine system-level requirements for assigned new and enhanced products.
  • Lead the development team in translating system-level requirements into product architecture and system-level design, including partitioning functionality into subsystems, creating subsystem specifications, and documenting interface requirements among subsystems.
  • Ensure new product architecture meets system-level requirements and is appropriately featured, robust, and adaptable enough to support product lifecycle plans and objectives.
  • Establish performance, interface, safety, and cost specifications for each subsystem in consultation with functional design leaders, and contribute significantly to system-level risk management activities for assigned programs.
  • Under the auspices of the Program Manager, lead allocation of system functionality among electronic, software, and mechanical subsystems; make hardware/software/mechanical, cost/time/performance, and safety trade-off decisions needed to meet clinical performance, reliability, manufacturability/serviceability, regulatory, and business objectives.
  • Lead efforts during product implementation to develop and refine system-level design, identify and resolve subsystem performance and interface issues, and resolve cross-functional design issues with system-level impacts.
  • Lead and oversee team efforts during subsystem integration and verification testing to ensure critical subsystems meet individual performance, interface, and system-integration goals and the fully integrated system meets performance, safety, and cost requirements.
  • Document system-level design, operating principles, and subsystem interface specifications for assigned new and existing products.
  • Research and document relationships between clinical requirements, architectural decisions, performance requirements, and product evolution plans.
  • Advise and consult with engineering teams regarding systems engineering principles and system-level requirements of ZOLL products.
  • Participate in decision-making processes involving changes to the system-level design of existing products.

About the Company

ZOLL Medical

Emergency care medical devices and software

ZOLL Medical develops and markets medical devices and software for emergency and critical care. Its products include defibrillators and automated external defibrillators (AEDs), mobile ECG systems, disposable electrodes, temperature management devices, and sleep apnea therapies, all complemented by software that integrates with the hardware to manage and analyze patient data. The products are designed for hospitals, emergency medical services (EMS), and other healthcare facilities worldwide, offering an end-to-end solution that combines hardware and data software. The goal is to improve patient outcomes and boost clinical and operational efficiency through reliable, integrated devices and data-enabled software for emergency and critical care.

Company size
1,001-5,000
Company stage
Acquired
Total funding
$2.2B
Headquarters
Chelmsford, MA
Founded
1980

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