Supplier Quality Engineer II — Medical Devices

Medtronic plc

Brooklyn Park (MN)

On-site

USD 90,000 - 120,000

Full time

2 days ago
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Job summary

Medtronic is seeking a Supplier Quality Engineer II for its Brooklyn Park, Minnesota site. This on-site role focuses on supplier qualification, manufacturing support, and continuous improvement within a regulated medical device environment.

You will monitor supplier performance, address quality issues, conduct supplier audits, and collaborate with engineering and quality teams to ensure compliance with quality and regulatory requirements.

Responsibilities

  • Ensure suppliers deliver parts, materials, and services that meet established quality requirements.
  • Qualify suppliers according to company standards and support receiving inspection and supplier quality programs.
  • Monitor supplier parts throughout the manufacturing cycle and drive resolution of supplier‑related quality issues.
  • Develop and prioritize supplier audit schedules and conduct audits against GMP and applicable quality standards.
  • Evaluate supplier processes and quality systems, communicate findings, and drive appropriate improvements.
  • Provide Supplier Quality Engineering support throughout the New Product Development lifecycle for newly qualified parts.
  • Partner with Component Engineering and Post‑Market Supplier Quality teams on product acceptance sampling strategies, Approved Supplier List coordination, Supplier Owned Quality deployment, and control plans.
  • Define receiving inspection requirements and support validation of applicable internal test methods.

Job description

Medtronic is seeking a Supplier Quality Engineer II for its Brooklyn Park, Minnesota site. This on-site role focuses on supplier qualification, manufacturing support, and continuous improvement within a regulated medical device environment.

You will monitor supplier performance, address quality issues, conduct supplier audits, and collaborate with engineering and quality teams to ensure compliance with quality and regulatory requirements.

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