Manufacturing Process Engineer II

Edwards Lifesciences Gruppe

Salt Lake City (UT)

On-site

USD 75,000 - 110,000

Full time

4 days ago
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Job summary

Edwards Lifesciences in Salt Lake City is seeking a Transfer Engineer to optimize manufacturing processes and transition new products into production. You will apply Six Sigma and LEAN methods, design experiments, and validate processes while supporting continuous improvement in a high‑stakes medical device environment.

The role requires a engineering or scientific degree with experience or a master’s with project work; strong documentation, CAD skills, and cross‑functional collaboration are

Qualifications

  • Bachelor's degree in Engineering or Scientific field with 2 years of related experience or
  • Master's degree or equivalent with internship, senior projects, or thesis in Engineering or Science.

Responsibilities

  • Optimize manufacturing processes using Six Sigma and LEAN methods; redesign equipment or fixtures to improve production.
  • Develop moderately complex experiments and tests to qualify and validate processes and analyze results.
  • Resolve CAPA, non-conformances, and audit observations in Manufacturing and Compliance.
  • Create training and work instruction materials for production to enable transfer of processes.
  • Establish project plans with deliverables, risks, and milestones using project management tools.
  • Oversee manufacturing support tasks; train technicians and coordinate their work.

Skills

Six Sigma
LEAN methods
Statistical methods
Project management
CAD
Documentation
MS Project
MS Office

Education

Bachelor's degree in Engineering or Scientific field
Master's degree in Engineering or Science

Tools

MS Visio
CAD software

Job description

Edwards Lifesciences in Salt Lake City is seeking a Transfer Engineer to optimize manufacturing processes and transition new products into production. You will apply Six Sigma and LEAN methods, design experiments, and validate processes while supporting continuous improvement in a high‑stakes medical device environment.

The role requires a engineering or scientific degree with experience or a master’s with project work; strong documentation, CAD skills, and cross‑functional collaboration are

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