Maintenance Technician — Medical Device Manufacturing

Edwards Lifesciences Gruppe; Salt Lake City (UT); On-site; USD 70,000 - 110,000; Full time

Job summary

Edwards Lifesciences Gruppe seeks a technical specialist to support Operations and Engineering. You will troubleshoot equipment, run feasibility studies, and lead validation projects to improve manufacturing processes. Collaboration with Quality and CAD teams is essential.

You will perform preventive maintenance, handle root cause analyses, and ensure compliant documentation. Strong communication and problem-solving skills are required in a GMP environment.

Qualifications

• Minimum HS diploma with 6 years related experience or an Associate's degree with 4 years related experience.
• Experience in manufacturing or medical device environments preferred.
• Strong problem solving, root cause analysis, and GDP/documentation practices.

Responsibilities

• Troubleshoot and perform maintenance to minimize downtime and maintain validation.
• Design, set-up and execute feasibility studies and tests for equipment and processes.
• Lead projects related to new equipment validation and investigations.
• Perform scheduled and unscheduled preventive maintenance on complex equipment.
• Collaborate with Quality on corrective actions, EWOs and ENCRs.
• Review and transfer validation documentation across systems and drawings.
• Use JDE, QMS, PLM to update documentation; coordinate with Engineering and CAD teams.
• Provide coaching to technicians and ensure on-time attendance and adherence to safety and quality guidelines.

Skills

Troubleshooting

Maintenance

Feasibility studies

Experimental design

Project leadership

Preventive maintenance

Documentation

CAD

JDE

QMS

PLM

GDP

MS Office

Education

HS Diploma with 6 years related experience

Associate's Degree with 4 years related experience

Tools

JDE

QMS

PLM

CAD

Job description

Edwards Lifesciences Gruppe seeks a technical specialist to support Operations and Engineering. You will troubleshoot equipment, run feasibility studies, and lead validation projects to improve manufacturing processes. Collaboration with Quality and CAD teams is essential.

You will perform preventive maintenance, handle root cause analyses, and ensure compliant documentation. Strong communication and problem-solving skills are required in a GMP environment.