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6 days ago
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Full time
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Related skills

manufacturing inspection lean continuous improvement iso

📋 Description

  • Manage and execute assigned quality projects in an FDA Title 21 (820) environment
  • Cross-functional support for rapid growth and continuous improvement
  • Support in-house manufacturing operations
  • Develop quality system procedures with cross-functional teams
  • Assist in design development projects representing QA and customers
  • Contribute to Continuous Improvement and Lean culture

🎯 Requirements

  • Bachelor's degree in Engineering, Science, Technology or related field
  • 3+ years of progressive medical device engineering experience
  • Experience in FDA Title 21 CFR 820 environment
  • Experience with manufacturing, development or quality engineering
  • Knowledge of quality systems, change control, and inspection processes
  • Ability to work cross-functionally and in cross-functional teams
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