Senior Lifecycle Quality Engineer

J&J FAMILY OF COMPANIES

Ciudad Juarez, Chihuahua, Mexico
**
Bachelor's degree in engineering
Minimum 4 years work experience
Strong analytical problem-solving skills
** Johnson & Johnson is seeking a Senior Lifecycle Quality Engineer in Ciudad Juarez, Mexico, to lead quality assurance efforts for medical products, ensuring compliance with regulatory standards while supporting product life cycles. The ideal candidate should have a background in engineering, experience in regulated industries, and strong analytical skills. **

Job Summary

  • The role provides overall quality assurance leadership for contract manufacturing sites to ensure compliance with good manufacturing practices and international standards.
  • Candidates must apply engineering principles, statistics, and risk management to support the entire product lifecycle from new product introduction to steady state manufacturing.
  • Johnson & Johnson offers an inclusive work environment that respects diversity and values the merit of employees working across the globe.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Senior Lifecycle Quality Engineer in Ciudad Juarez, Mexico, to lead quality assurance efforts for medical products, ensuring compliance with regulatory standards while supporting product life cycles. The ideal candidate should have a background in engineering, experience in regulated industries, and strong analytical skills. **

Skills & Requirements

Must-have

  • Bachelor's degree in engineering
  • Minimum 4 years work experience
  • Strong analytical problem-solving skills
  • Statistical application DOE and FMEA
  • Risk Management ISO 14971 knowledge
  • Fluent English communication required

Nice-to-have

  • Six Sigma or Process Excellence certification
  • ASQ certification CQE or CRE preferred
  • Cross-cultural collaboration abilities
  • Mentoring and technical training skills
  • Experience with SAP Product Lifecycle Management
  • Advanced quality systems AQS experience

Key Requirements

  • Bachelor's degree in Mechanical, Electrical, or Biomedical Engineering
  • Minimum 4 years of relevant work experience
  • Experience in regulated medical device industry
  • Knowledge of ISO 13485 and GMP standards
  • Auditing skills including MDSAP and QSR
  • Fluency in English for written and oral tasks

Work Rights

Not specified

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