Senior Quality Engineer

Johnson & Johnson MedTech

Irvine, California, United States
Base: $79,000.00 - $127,650.00; bonus/equity: not ...
Not specified (assumed to be hybrid or onsite based on the nature of the role).
Quality engineering tools and processes
Design control and verification validation
Risk management and fmea development
Johnson & Johnson MedTech is seeking a Senior Quality Engineer to join their team in Irvine, California. The role focuses on quality assurance for new product development in the medical device sector, emphasizing innovation and compliance throughout the product lifecycle

Job Summary

  • The Senior Quality Engineer plans, coordinates and executes quality assurance activities throughout the product lifecycle to ensure compliance with company and external standards.
  • This role involves collaboration with R&D and Operations teams to support new product development, engineering projects, and quality assurance activities.
  • Employees are eligible for comprehensive benefits including retirement plans, vacation, sick time, parental leave, and various other paid time off options.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Senior Quality Engineer to join their team in Irvine, California. The role focuses on quality assurance for new product development in the medical device sector, emphasizing innovation and compliance throughout the product lifecycle.

Salary

Base: $79,000.00 - $127,650.00; Bonus/Equity: Not specified; Benefits: Retirement plans, vacation, sick time, parental leave, and other paid time off

Skills & Requirements

Must-have

  • Quality Engineering tools and processes
  • Design control and verification validation
  • Risk management and FMEA development
  • Statistical analysis and Six Sigma methodologies
  • New Product Development (NPD) collaboration
  • Root cause analysis and failure investigation

Nice-to-have

  • Lean manufacturing experience
  • Knowledge of SolidWorks and CAD programs
  • Experience with Minitab and R statistical software
  • Strong collaboration and negotiation skills
  • Understanding of GMP and regulatory compliance
  • Geometrical Dimensioning and Tolerancing (GD&T)

Key Requirements

  • Bachelor’s degree in engineering or scientific field
  • Minimum 4 years quality or R&D experience in regulated industry
  • Ability to apply project management skills in NPD
  • Knowledge of Six Sigma and process excellence tools
  • Ability to travel up to 20% domestically and internationally

Work Rights

Not specified

Tailored Resume

Cover Letter