Quality Engineer II: Process Optimization

Edwards Lifesciences

Salt Lake City (UT)

On-site

USD 90,000 - 130,000

Full time

7 days ago
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Job summary

Edwards Lifesciences in Salt Lake City seeks a Quality Engineer II to support the PASCAL Gen 3 product line at the Draper facility, partnering with manufacturing, supplier quality, and cross-functional engineering teams to stabilize a new product line, improve yield, resolve quality issues, and help prepare for future launches.

You will work to ensure commercially released and human-use products meet rigorous quality expectations while directly impacting patients worldwide.

Qualifications

  • Bachelor's degree in engineering or scientific field with 2 years Quality or Manufacturing Engineering experience preferred.
  • Experience supporting production line sustaining activities.
  • Experience in a highly regulated industry such as medical device, aerospace, automotive, semiconductor, or similar.

Responsibilities

  • Support sustaining Quality Engineering activities for the PASCAL Gen 3 line, including stabilization and continuous improvement.
  • Partner with cross-functional teams to identify quality trends and drive yield improvements.
  • Own or support NCRs, investigations, dispositions, containment, and corrective actions per quality system requirements.
  • Develop and review engineering studies, test method validations, and manufacturing process validation deliverables.
  • Create and sustain dimensional inspection routines using Keyence or similar technology.

Skills

Quality Engineering
Manufacturing Engineering
Data analysis
Problem solving
Documentation

Education

Bachelor's degree in engineering or scientific field
Master's degree in engineering or scientific field

Tools

Keyence programming
TMV / OQ/PQ protocol tools

Job description

Edwards Lifesciences in Salt Lake City seeks a Quality Engineer II to support the PASCAL Gen 3 product line at the Draper facility, partnering with manufacturing, supplier quality, and cross-functional engineering teams to stabilize a new product line, improve yield, resolve quality issues, and help prepare for future launches.

You will work to ensure commercially released and human-use products meet rigorous quality expectations while directly impacting patients worldwide.

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