QMS Leader – Medical Device Compliance

Medtronic; Plymouth (MN); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Competitive salary

Benefits package

Job summary

Medtronic in Plymouth, MN is seeking a Quality Systems Manager to lead the Quality Management System at the Nathan Lane manufacturing site, supporting high‑volume, regulated production of life‑changing medical technologies.

You will partner with Operations, Quality, Manufacturing Engineering, Regulatory, and Supply Chain to ensure compliant, effective quality programs and drive continuous improvement and a culture of quality.

Qualifications

• Bachelor's degree with 5+ years relevant experience.
• Experience with QMS processes (CAPA, change control, document control).
• Experience with FDA inspections, ISO 13485, MDSAP or similar audits.

Responsibilities

• Lead continuous improvement initiatives across core quality system processes.
• Ensure compliance and alignment of quality programs with regulations.
• Drive a culture of quality and operational excellence across functions.
• Collaborate with Operations, Quality, Manufacturing Eng., Regulatory, and Supply Chain.

Skills

QMS

CAPA

Audits

Document control

Regulatory affairs

Quality metrics

Cross-functional collaboration

Education

Bachelor's in Engineering, Quality, Life Sciences

Job description

Medtronic in Plymouth, MN is seeking a Quality Systems Manager to lead the Quality Management System at the Nathan Lane manufacturing site, supporting high‑volume, regulated production of life‑changing medical technologies.

You will partner with Operations, Quality, Manufacturing Engineering, Regulatory, and Supply Chain to ensure compliant, effective quality programs and drive continuous improvement and a culture of quality.