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ZOLL Medical

Emergency care medical devices and software

R&D System Verification & Validation Test Manager

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeIrvine, CA, USA

About the Job

Requirements

  • A bachelor's degree in Software Engineering, Computer Science, or a similar field is required.
  • An advanced degree is preferred.
  • At least 5 years of experience managing, coaching, and mentoring employees in a technical business environment is required.
  • At least 10 years of experience in hardware and software design quality assurance is required.
  • At least 5 years of hands-on experience in software quality assurance associated with real-time embedded software systems is required.
  • Thorough understanding of software quality assurance principles, practices, and metrics, as well as software development and testing best practices that foster high-quality software.
  • Hands-on experience using modern software development and quality assurance tools.
  • Excellent written, verbal, and interpersonal skills.
  • Business acumen.

Responsibilities

  • Lead, direct, and oversee pre-commercialization design quality assurance efforts for new products and product modifications within the Research and Development organization.
  • Develop and execute system-level testing programs to verify that new or modified products are safe and operate as intended under bench testing and simulated clinical-use conditions.
  • Develop testing programs based on product requirements, applicable safety and performance standards, risk management and usability principles, and documented and implied user needs and requirements.
  • Direct the efforts of 5–10 subordinates responsible for verifying the quality, safety, and expected performance of defibrillator and patient-monitoring products, focusing primarily on software quality and performance.
  • Report testing results to Project and R&D managers, compute quality metrics, and track progress on unresolved issues.
  • Plan, budget, schedule, and track Design Quality Assurance team efforts for system-level design verification and validation procedures across multiple concurrent development projects.
  • Establish policies and procedures for planning and coordinating hardware and software quality assurance efforts by development and quality assurance teams.
  • Work with development teams to define, plan, and integrate Design Quality Assurance efforts into each new product development project.
  • Lead and manage the development and execution of system-level hardware and software verification and validation procedures for new and modified products, incorporating simulated use, clinical performance, standards, risk management, and usability principles.
  • Review, audit, and approve design quality assurance procedures, testing results, and documentation associated with new product releases and product design changes.
  • Develop, document, maintain, and execute standardized system-level validation procedures for new products.
  • Develop test strategies, procedures, and test setups for simulated-use tests, stress tests, and other testing of new and modified products.
  • Participate as a project team member in developing new product specifications, emphasizing clinical acceptability and the objective verifiability and validation of specifications.
  • Work with project teams, functional managers, and Quality Assurance to investigate product design problems reported by customers and help resolve them.
  • Work onsite at the Irvine office 4–5 days a week.

Desired Qualifications

  • Familiarity with FDA and international standards and regulations applicable to medical device hardware and software development, verification, and validation is preferred.
  • Understanding of clinical environments and issues related to the clinical application of medical electronic products is desirable.

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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