Medical Device Transfer Specialist

Edwards Lifesciences Gruppe; Draper (UT); On-site; USD 75,000 - 110,000; Full time

Job summary

Edwards Lifesciences is seeking a Manufacturing Equipment Specialist to support transfer and validation activities for new products. You will troubleshoot, maintain, and validate equipment, supporting cross-functional teams with documentation and process improvements.

The role emphasizes strong communication, problem solving, and adherence to GDP in a medical device manufacturing environment. On-site in Utah, USA, with opportunities to contribute to critical patient-focused launches.

Qualifications

• HS Diploma or equivalent with 6 years related experience or
• Associate’s Degree or equivalent with 4 years related experience.
• Experience in manufacturing and/or medical device environment preferred.
• Strong communication and training skills; able to guide others.

Responsibilities

• Troubleshoot and maintain equipment to limit downtime and ensure validation compliance.
• Design and execute feasibility studies, tests, and protocols for equipment and processes.
• Perform preventive maintenance on complex equipment to validate operation.
• Investigate failures and write impact assessment reports for incidents.
• Collaborate with Quality on corrective actions, EWOs, ENCRs, and OOTs.
• Ensure documentation is properly archived and transferred to ECRs, SOPs, drawings, and tooling.

Skills

Communication

Problem solving

GDP / Good Documentation Practices

Analytical thinking

Project management basics

Troubleshooting equipment

Training & guidance

MS Office proficiency

Manufacturing equipment knowledge

Education

HS Diploma or equivalent

Associate’s Degree or equivalent

Tools

MS Office

JDE

QMS

PLM

Maximo

CAD

Job description

Edwards Lifesciences is seeking a Manufacturing Equipment Specialist to support transfer and validation activities for new products. You will troubleshoot, maintain, and validate equipment, supporting cross-functional teams with documentation and process improvements.

The role emphasizes strong communication, problem solving, and adherence to GDP in a medical device manufacturing environment. On-site in Utah, USA, with opportunities to contribute to critical patient-focused launches.