Ingeniero De Calidad Ii (segundo Turno)

Johnson & Johnson MedTech

Ciudad Juarez, Chihuahua, Mexico
Bachelor's degree in related field
2-4 years quality or manufacturing experience
Medical device regulated industry experience
This role supports the development of quality-engineered systems and products for Johnson & Johnson MedTech's Cardiovascular division

Job Summary

  • This role supports the development of quality-engineered systems and products for Johnson & Johnson MedTech's Cardiovascular division.
  • The incumbent will lead design verification tests, process validations, and ensure compliance with FDA, ISO 13485, and other global regulatory standards.
  • Candidates must possess strong problem-solving skills to independently develop solutions for complex quality issues while adhering to corporate safety practices.

Matching Summary

This role supports the development of quality-engineered systems and products for Johnson & Johnson MedTech's Cardiovascular division.

Skills & Requirements

Must-have

  • Bachelor's degree in related field
  • 2-4 years quality or manufacturing experience
  • Medical device regulated industry experience
  • FDA ISO 13485 regulatory compliance knowledge
  • Process validation and design verification skills

Nice-to-have

  • Six Sigma and statistical analysis tools
  • GD&T geometric dimensioning concepts
  • Master's degree preferred
  • ASQ certification desirable
  • Supplier audit support experience

Key Requirements

  • Bachelor's degree required
  • 2-4 years relevant experience
  • Knowledge of GMP and QSR requirements
  • Experience with CAPA and internal audits

Work Rights

Not specified

Tailored Resume

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