Z

ZOLL Medical

Emergency care medical devices and software

Senior Quality Assurance Engineer

Quality Engineering +1Confirmed live in the last 24 hours
Full-timePittsburgh, PA, USA$96k - $130k /yrIn-person

About the Job

Requirements

  • A Bachelor's degree or equivalent experience in a technical or scientific discipline is required.
  • At least 5 years of experience in an FDA-regulated medical device manufacturing environment is required.
  • At least 5 years of experience in process development and validation for electro-mechanical assembly, test, and service is required.
  • Lean experience is required.
  • Understand and have applied in practice the concepts of process capability, process control, and measurement system capability.
  • The employee must occasionally lift and/or move up to 25 pounds.

Responsibilities

  • Champion the internal audit quality process and effectiveness reviews, ensuring cross-functional compliance with the quality system manual, internal processes, and regulated bodies, including FDA QSR, ISO 13485, MDD, and CMDR.
  • Lead the development and execution of Lean/Six Sigma and other cost-improvement initiatives related to product quality.
  • Champion the CAPA System process, ensuring cross-functional compliance with the quality system manual and internal processes.
  • Understand applicable legal and regulatory requirements in medical device operations and establish robust processes and controls to ensure compliance.
  • Lead and improve key business relationships across cross-functional departments as a quality assurance subject matter expert.
  • Ensure operations quality measurement systems are capable (Gauge R&R), process capability (Cpk) is high, and process controls are in place to ensure products meet specifications.
  • Lead risk analysis activities for new and existing products, including FMEAs and Fault Tree Analyses.
  • Lead the non-product software validation process by providing project management and preparing and coordinating process validation requirements.
  • Participate in the FDA premarket approval (PMA) process for new and modified medical devices.
  • Participate in the nonconforming material/Material Review Board process.
  • Champion the implementation of Lean Manufacturing processes.
  • Participate in Kaizen events as a representative of the quality department.
  • Sit and talk or hear regularly; stand and walk occasionally.

Desired Qualifications

  • Formal project management experience is preferred.
  • Lean Six Sigma Black Belt is preferred.

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

Recently Posted Jobs

Explore more opportunities at ZOLL Medical

See more jobs