Sr. Quality Engineer

Danaher UK

New Brighton, Minnesota, United States
Base: $115k – $125k; bonus/equity: eligible for bo...
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5+ years manufacturing experience in fda or iso industry
In-depth knowledge of qms processes for capa and nonconformance
Practical knowledge of risk management and statistical data analysis
** Danaher UK is seeking a Sr. Quality Engineer for its Radiometer division in New Brighton, Minnesota. The role focuses on ensuring product quality through audits, inspections, and quality improvement projects within a collaborative team environment. **

Job Summary

  • The Sr. Quality Engineer is responsible for assuring the quality of processes and products by performing audits, inspections, tests, and defect analysis.
  • This role involves driving quality-related improvement projects through cross-functional teamwork while utilizing Danaher Business System concepts.
  • The position offers a competitive salary range of $115K – $125K along with comprehensive benefits including medical/dental/vision insurance and 401(k).

Matching Summary

Match Score: 75

** Danaher UK is seeking a Sr. Quality Engineer for its Radiometer division in New Brighton, Minnesota. The role focuses on ensuring product quality through audits, inspections, and quality improvement projects within a collaborative team environment. **

Salary

Base: $115K – $125K; Bonus/Equity: Eligible for bonus/incentive pay; Benefits: Paid time off, medical/dental/vision insurance, 401(k)

Skills & Requirements

Must-have

  • 5+ years manufacturing experience in FDA or ISO industry
  • In-depth knowledge of QMS processes for CAPA and nonconformance
  • Practical knowledge of risk management and statistical data analysis
  • Experience with change control and complaint investigations
  • Bachelor's degree in engineering or sciences

Nice-to-have

  • Experience with thick film sensors for blood gas analysis
  • Statistical software knowledge including JMP
  • Familiarity with Danaher Business System concepts
  • Cross-functional teamwork in value stream improvement
  • Ability to drive quality projects with R&D and Engineering

Key Requirements

  • 5+ years manufacturing experience in FDA/ISO industry
  • Bachelor's degree in engineering or sciences
  • Knowledge of QMS, CAPA, and risk management
  • Statistical data analysis skills
  • Change control experience

Work Rights

Not specified

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