Engineer I - Manufacturing*

Integer

**
Bachelor's degree in engineering
Three years relevant experience
Fda regulations knowledge
** Integer is seeking an Engineer I for their Manufacturing team, focusing on innovative medical device technology and quality management. The ideal candidate should possess a bachelor's degree in engineering or a related field, with at least three years of relevant experience, and demonstrate a strong commitment to quality, collaboration, and continuous improvement. **

Job Summary

  • The primary purpose of this position is to perform work involving general engineering methods while developing advanced technologies in the medical device industry.
  • You will ensure customer expectations are met by adhering to FDA regulations, Quality Management Systems, and safety requirements while investigating product failures.
  • This role requires championing Manufacturing Excellence strategies through standardization, associate engagement, and systems optimization to drive continuous improvement.

Matching Summary

Match Score: 75

** Integer is seeking an Engineer I for their Manufacturing team, focusing on innovative medical device technology and quality management. The ideal candidate should possess a bachelor's degree in engineering or a related field, with at least three years of relevant experience, and demonstrate a strong commitment to quality, collaboration, and continuous improvement. **

Skills & Requirements

Must-have

  • Bachelor's degree in engineering
  • Three years relevant experience
  • FDA regulations knowledge
  • Quality Management Systems (QMS)
  • Root cause analysis techniques
  • Process improvement methodologies

Nice-to-have

  • Proactive insight into technical challenges
  • Strong written and oral communication
  • Positive can-do attitude
  • Collaboration with cross-functional teams
  • Experience with Integer Production System

Key Requirements

  • Bachelor's degree in engineering or related field
  • Minimum three years of relevant experience
  • Functional understanding of QMS documentation
  • Ability to work independently with occasional guidance

Work Rights

Not specified

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