Manufacturing Transfer Engineer II Process Improvement

Edwards Lifesciences Gruppe; Draper (UT); On-site; USD 80,000 - 110,000; Full time

Job summary

Edwards Lifesciences in Draper, Utah, is seeking a Transfer Engineer to join the Global Operations & Quality team. You’ll help transition new products into manufacturing, set up lines, qualify equipment, perform process validation, and ensure production readiness.

You’ll collaborate with manufacturing, engineering, and quality teams to optimize processes, develop protocols, and train technicians while maintaining compliant, high-quality medical devices.

Qualifications

• Bachelor's degree in Engineering or Science with 2 years of related experience or Master's with internship/thesis in Engineering or Science
• Hands-on manufacturing and/or equipment experience
• Experience with process validations preferred
• Good documentation and communication skills; ability to interact across organization

Responsibilities

• Optimize manufacturing processes using Six Sigma/LEAN to improve efficiency and equipment design
• Develop moderately complex experiments and tests to qualify and validate processes
• Analyze and resolve manufacturing and compliance issues (e.g., CAPA, non-conformances)
• Develop training and work instructions for production teams
• Create project plans and manage deliverables with project tools
• Oversee manufacturing support tasks and coordinate technicians' work
• Support leadership with additional duties as needed

Skills

Six Sigma

LEAN methods

Project management

MS Project

CAD

Statistical techniques

Education

Bachelor's degree in Engineering or Science

Master's degree or equivalent with internship/thesis

Tools

MS Project

CAD

MS Office Suite

Job description

Edwards Lifesciences in Draper, Utah, is seeking a Transfer Engineer to join the Global Operations & Quality team. You’ll help transition new products into manufacturing, set up lines, qualify equipment, perform process validation, and ensure production readiness.

You’ll collaborate with manufacturing, engineering, and quality teams to optimize processes, develop protocols, and train technicians while maintaining compliant, high-quality medical devices.