Inogen

Quality Engineer III

Job Description

Posted on: 
2025-08-18

Responsibilities

  • Drive new product design and development activities.
  • Lead the transition from product design to production.
  • Oversee manufacturing and quality activities for improvement and risk.
  • Lead quality initiatives and post-market activities, including complaint investigations.
  • Conduct root cause investigations and implement corrective and preventive actions.
  • Develop and implement quality management system procedures.
  • Participate in internal and external audits.

Job Requirements

  • Bachelor’s degree in engineering or related scientific field.
  • Minimum of three years of experience as a Quality Engineer in the medical device industry.
  • Proficiency in applicable medical device regulations (e.g., FDA QSR, EU MDR).
  • Experience with statistical analysis software (e.g., Minitab).
  • Ability to compile data for reporting and analysis.
  • Strong communication and organizational skills.
  • Demonstrated competency in quality management systems and complaint investigation.
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