Senior Engineer, New Product Introduction (npi)/lifecycle Quality

J&J FAMILY OF COMPANIES

Milpitas, California, United States of America
Base: $91,000.00 - $147,200.00; bonus/equity: not ...
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Quality leadership in product development
Risk management and human factors
Design control strategy and implementation
** Johnson & Johnson is seeking a Senior Engineer for New Product Introduction (NPI) and Lifecycle Quality in Milpitas, California. The role focuses on providing quality leadership in the development of medical devices, ensuring compliance with regulatory standards while fostering an inclusive and innovative work environment. **

Job Summary

  • Provides quality and technical leadership to ensure new and existing medical devices meet their intended use.
  • Leads development team in design control strategy and implementation, collaborating with functional business partners to proactively address quality issues.
  • Activities include risk management, human factors, and support for Quality Management Systems such as Design Control, Risk Management, and CAPA.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Senior Engineer for New Product Introduction (NPI) and Lifecycle Quality in Milpitas, California. The role focuses on providing quality leadership in the development of medical devices, ensuring compliance with regulatory standards while fostering an inclusive and innovative work environment. **

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 in product development
  • Risk management and human factors
  • Design control strategy and implementation
  • Medical device regulations (QSR/ISO)

Nice-to-have

  • Proactive quality issue resolution
  • Team environment collaboration
  • Attention to detail
  • Strong written and verbal communication

Key Requirements

  • 4 years working experience in regulated industry
  • Bachelors or equivalent university degree in Engineering
  • Practical understanding of QSR/ISO medical device regulations
  • Experience in Medical Device industry

Work Rights

Not specified

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