Inogen

Quality Engineer III

Job Description

Posted on: 
2025-09-03

Responsibilities

  • Drive new product design and development activities.
  • Lead in the effective transition from product design to production.
  • Lead and oversee manufacturing and quality activities for improvement and risk.
  • Lead in achievement quality initiatives.
  • Lead in post-market activities, such as complaint investigations and medical device reporting.
  • 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.
  • Excellent oral and written communication skills.
  • Ability to multitask, meet deliverables, and work in a team environment.
  • Proficient with Minitab or other statistical analysis software.
  • Demonstrated competency in developing and implementing QMS procedures.
  • Knowledge of applicable medical device regulations such as FDA QSR, EU MDR.
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