Staff Quality Engineer - Quality Lcm

Janj Ja

Irvine, California, United States of America
Base: $125,000 - $150,000; bonus/equity: not speci...
Hybrid (may telecommute 2 days per week)
Quality life cycle management expertise
Quality assurance in medical devices
Statistical process control and six sigma
Johnson & Johnson is seeking a Staff Quality Engineer for their Biosense Webster division in Irvine, California. The role focuses on quality assurance throughout the product lifecycle of medical devices, specifically electrophysiology catheters and systems, and includes responsibilities such as leading design verification tests and ensuring compliance with regulatory standards

Job Summary

  • Johnson & Johnson provides an inclusive work environment respecting diversity and dignity of employees worldwide.
  • The Staff Quality Engineer will lead quality assurance activities to ensure effective product quality processes throughout the lifecycle of electrophysiology catheters, cables, and systems.
  • Employees are eligible for comprehensive benefits including medical, dental, vision, retirement plans, long-term incentives, and various paid time off programs.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Staff Quality Engineer for their Biosense Webster division in Irvine, California. The role focuses on quality assurance throughout the product lifecycle of medical devices, specifically electrophysiology catheters and systems, and includes responsibilities such as leading design verification tests and ensuring compliance with regulatory standards.

Salary

Base: $125,000 - $150,000; Bonus/Equity: Not specified; Benefits: Medical, dental, vision, retirement plans, paid time off

Skills & Requirements

Must-have

  • Quality Life Cycle Management expertise
  • Quality assurance in medical devices
  • Statistical process control and Six Sigma
  • Design verification and process validation
  • Regulatory compliance FDA ISO 13485
  • Cross-functional collaboration
  • Product lifecycle quality management

Key Requirements

  • Master's degree in Mechanical or Biomedical Engineering
  • 4 years experience in quality engineering or related role
  • Knowledge of FDA, ISO 13485, CMDCAS, PMDA regulations

Work Rights

Not specified

Tailored Resume

Cover Letter