Senior Quality Engineer

Cytiva, one of Danaher's operating companies

Pensacola, US
**
Iso 13485 and iso 9001 compliance
Root cause analysis and capa execution
Medical device quality engineering experience
** Cytiva is seeking a Senior Quality Engineer to ensure the quality of membrane products and medical devices through effective management of the Quality Management System (QMS) in Pensacola, US. The ideal candidate will have over seven years of experience in medical device quality engineering, with a strong background in ISO standards and continuous improvement methodologies. **

Job Summary

  • The Senior Quality Engineer ensures the quality of membrane products and medical devices by facilitating cross-functional execution of the Quality Management System.
  • This role requires leading root cause analysis, implementing CAPA for nonconformities, and ensuring design control process compliance throughout the product lifecycle.
  • Cytiva offers a culture of belonging where employees can continuously improve themselves while working on challenges that truly matter in life sciences.

Matching Summary

Match Score: 75

** Cytiva is seeking a Senior Quality Engineer to ensure the quality of membrane products and medical devices through effective management of the Quality Management System (QMS) in Pensacola, US. The ideal candidate will have over seven years of experience in medical device quality engineering, with a strong background in ISO standards and continuous improvement methodologies. **

Skills & Requirements

Must-have

  • ISO 13485 and ISO 9001 compliance
  • Root cause analysis and CAPA execution
  • Medical device quality engineering experience
  • FDA QSR knowledge
  • Risk management tools proficiency

Nice-to-have

  • Lean and Six Sigma methodologies
  • Cross-functional collaboration skills
  • New product introduction support
  • Training on quality processes
  • Culture of belonging and innovation

Key Requirements

  • Bachelor's degree in Engineering or related Science field
  • 7+ years in medical device quality engineering
  • Strong knowledge of FDA QSR and risk management tools

Work Rights

Not specified

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