Maintenance Technician – Medical Device Validation

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

Job summary

Edwards Lifesciences in Salt Lake City, Utah, is hiring for a full-time Maintenance/Equipment Validation role to support Operations and Engineering. You will troubleshoot, validate, and improve automation and manufacturing equipment while ensuring regulatory documentation is complete and accurate.

The position requires hands-on maintenance, strong problem-solving, and collaboration with Quality and Engineering. A technical background in manufacturing equipment and GMP practices is preferred.

Qualifications

• Must have strong written and verbal communication skills.
• Experience with GMP/Good Documentation Practices.
• Proficient with MS Office; CAD skills a plus.
• Experience in manufacturing/medical device environments preferred.

Responsibilities

• Troubleshoot and maintain equipment to limit downtime and support validation.
• Design, set-up and execute feasibility studies and tests to improve equipment and processes.
• Lead projects related to new equipment validation and investigations.
• Perform preventive maintenance on complex equipment and document actions.
• Collaborate with Quality to implement corrective actions and non-conformance reports.
• Validate equipment documentation and transfer information to appropriate systems.

Skills

Communication

Problem solving

GDP (GxP)

Documentation

Project basics

Troubleshooting

Education

High School Diploma or equivalent

Associate's Degree or equivalent

Tools

JDE

QMS

PLM

CAD

Job description

Edwards Lifesciences in Salt Lake City, Utah, is hiring for a full-time Maintenance/Equipment Validation role to support Operations and Engineering. You will troubleshoot, validate, and improve automation and manufacturing equipment while ensuring regulatory documentation is complete and accurate.

The position requires hands-on maintenance, strong problem-solving, and collaboration with Quality and Engineering. A technical background in manufacturing equipment and GMP practices is preferred.