Senior Lifecycle Quality Engineer

Johnson & Johnson MedTech

Ciudad Juarez, Mexico
On-site
Quality engineering activities
Reliability, risk management, analytics
Requirements management, verification & validation
Johnson & Johnson MedTech is seeking a Senior Lifecycle Quality Engineer in Ciudad Juarez, Mexico, to ensure product quality and compliance throughout the manufacturing process. The role involves leadership in quality engineering activities and collaboration across various teams to support product development and maintain regulatory standards

Job Summary

  • Provides leadership in design and implementation of world-class quality engineering to support entire product life cycle with focus on quality engineering activities such as reliability, risk management, analytics/statistical techniques, requirements management, verification & validation, and design control across the lifecycle of the product.
  • Applies intermediate Quality Engineering/Scientific Method techniques and principles to daily tasks and activities, and applies relevant regulations, standards, and industry best practices to assignments.
  • Ensures comprehensive measurement systems to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects, presenting reports to management which outline findings.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Senior Lifecycle Quality Engineer in Ciudad Juarez, Mexico, to ensure product quality and compliance throughout the manufacturing process. The role involves leadership in quality engineering activities and collaboration across various teams to support product development and maintain regulatory standards.

Skills & Requirements

Must-have

  • quality engineering activities
  • reliability, risk management, analytics
  • requirements management, verification & validation
  • design control across the lifecycle
  • statistical application in DOE, sampling
  • project management in a matrixed environment
  • manufacturing equipment and processes

Nice-to-have

  • cross-cultural work ability
  • continuous product improvement
  • technical training and mentoring
  • advanced quality systems experience
  • knowledge of regulatory compliance

Key Requirements

  • Bachelor's degree in engineering or relevant science/technical field
  • Minimum of 4 years' work experience
  • Experience in a regulated industry preferred
  • Experience with Risk Management (ISO 14971) preferred
  • Experience with Medical Device Quality Management System (ISO 13485) preferred
  • Fluent in English (written and oral)

Work Rights

Not specified

Tailored Resume

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