Senior Principal Quality Engineer – Design Quality & Systems Excellence

Johnson & Johnson MedTech

Danvers, Massachusetts, United States
Base: $122,000.00 - $212,750.00; bonus/equity: not...
Not specified (assumed hybrid based on the nature of the role).
Design quality excellence
System engineering principles
Design controls
Johnson & Johnson MedTech is seeking a Senior Principal Quality Engineer to lead design quality excellence in the development of electro-mechanical and software-driven medical devices. The ideal candidate will have extensive experience in quality engineering and risk management, and will play a critical role in ensuring product reliability and compliance

Job Summary

  • This role partners deeply with engineering and design quality engineering to ensure robust product design through strong system engineering principles, design controls, and risk management integration.
  • The ideal candidate will lead high-impact, cross-functional initiatives to improve product reliability and robustness through reliability growth programs, design-for portability (ambulation and transport), robust algorithm and sensor system validation, motor control verification and end-to end connectivity.
  • The anticipated base pay range for this position is : $122,000.00 - $212,750.00

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Senior Principal Quality Engineer to lead design quality excellence in the development of electro-mechanical and software-driven medical devices. The ideal candidate will have extensive experience in quality engineering and risk management, and will play a critical role in ensuring product reliability and compliance.

Salary

Base: $122,000.00 - $212,750.00; Bonus/Equity: Not specified; Benefits: Eligible for Company's consolidated retirement plan (pension) and savings plan (401(k)), long-term incentive program, vacation, sick time, holiday pay, Work, Personal and Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off

Skills & Requirements

Must-have

  • design quality excellence
  • system engineering principles
  • design controls
  • risk management integration
  • product reliability programs
  • advanced statistical methods

Nice-to-have

  • technical leader
  • change agent
  • cross-functional initiatives
  • data-driven decisions
  • hands-on technical guidance

Key Requirements

  • Bachelor’s or Master’s degree in Engineering
  • 12–15+ years of experience in medical device development
  • Extensive experience supporting New Product Development (NPD) programs
  • Strong expertise in Design controls and regulatory compliance
  • Strong expertise in System engineering principles
  • Strong expertise in Risk management and reliability engineering
  • Strong expertise in Advanced statistical methods and sampling strategies
  • Strong expertise in Electro-mechanical and software-integrated systems

Work Rights

Not specified

Tailored Resume

Cover Letter