Senior Engineer, New Product Introduction (npi)/lifecycle Quality
Johnson & Johnson Vision
Milpitas, California, United States of America
Base: $91,000.00 - $147,200.00; bonus/equity: not ...
Hybrid
Quality leadership on product teams
Design control strategy and implementation
Risk management and human factors
Johnson & Johnson Vision is seeking a Senior Engineer for New Product Introduction and Lifecycle Quality in Milpitas, CA. The role focuses on ensuring medical devices meet quality and regulatory standards while collaborating with cross-functional teams
Job Summary
The Senior Engineer, NPI and Lifecycle Quality provides quality and technical leadership to ensure new and existing medical devices meet their intended use.
Key responsibilities include quality leadership on product project teams, ensuring CTQs are established and met, and leading design control strategy and implementation.
The role involves collaborating with functional business partners to address quality issues during new product development and leading activities associated with risk management and human factors.
Matching Summary
Match Score: 85
Johnson & Johnson Vision is seeking a Senior Engineer for New Product Introduction and Lifecycle Quality in Milpitas, CA. The role focuses on ensuring medical devices meet quality and regulatory standards while collaborating with cross-functional teams.
Salary
Base: $91,000.00 - $147,200.00; Bonus/Equity: Not specified; Benefits: Vacation, Sick time, Holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off
Skills & Requirements
Must-have
Quality leadership on product teams
Design control strategy and implementation
Risk management and human factors
Medical device regulations (QSR/ISO)
Nice-to-have
Familiarity with GxP
Proactive quality issue resolution
Team environment collaboration
Key Requirements
4 years working experience in regulated industry
Bachelors or equivalent university degree in Engineering
Practical understanding of QSR/ISO medical device regulations