Manufacturing Engineer I (Night Shift) – Lean & Quality

Edwards Lifesciences; Draper (UT); On-site; USD 65,000 - 90,000; Full time

Job summary

Edwards Lifesciences in Utah is seeking an Engineer I to support sustaining engineering activities for existing products and lead basic process-improvement projects. You will troubleshoot issues, implement enhancements, and collaborate with cross-functional teams to improve quality, reliability, and efficiency in manufacturing.

The role schedule is evenings (3:30 pm - 2:30 am), with opportunities to grow technical skills in a medical device environment and to contribute to patient care.

Qualifications

• Bachelor’s Degree in Engineering or Scientific field is required.
• Related internship experience is a plus.
• Experience in the medical device industry is preferred.
• Good computer skills, MS Office including MS Project; CAD experience.
• Strong documentation, communication, and interpersonal skills.
• Basic understanding of statistical techniques.

Responsibilities

• Improve manufacturing processes using engineering methods (LEAN, statistics) for continuous improvement.
• Develop basic experiments and tests to qualify and validate processes; analyze results and report.
• Address Manufacturing and Compliance issues such as CAPA and non-conformances.
• Develop training materials and work instructions for production.
• Create project plans and manage deliverables using project management tools.
• Identify opportunities to redesign equipment and tooling to improve processes.
• Support technicians, provide instruction, and coordinate work.
• Perform additional duties as assigned.

Skills

LEAN methods

Statistics

Cross-functional collaboration

Documentation

Problem solving

Education

Bachelor’s Degree in Engineering or Scientific field

Tools

MS Project

CAD

Job description

Edwards Lifesciences in Utah is seeking an Engineer I to support sustaining engineering activities for existing products and lead basic process-improvement projects. You will troubleshoot issues, implement enhancements, and collaborate with cross-functional teams to improve quality, reliability, and efficiency in manufacturing.

The role schedule is evenings (3:30 pm - 2:30 am), with opportunities to grow technical skills in a medical device environment and to contribute to patient care.