Senior Pre-Market Supplier Quality Engineer

Medtronic

Confirmed live yesterday High trust
Remote

Quick summary

Work type
Remote
Location
Mounds View, MN
Salary
$99,200–$148,800 / yr
Posted
11 days ago
Freshness
Confirmed live yesterday

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $155k
This role $124k
$88k most similar roles pay here $205k

This role pays less than 82% of similar roles. Most pay $131,812–$177,387 — the shaded band above. At the midpoint, this role pays about $124k versus about $155k for comparable roles.

Based on 240 similar postings.

Employer

About Medtronic

Medtronic plc is the world's largest medical technology company by revenue, specializing in device-based therapies for over 70 health conditions.

Medtronic currently has 47 open roles on FindRole.

Listed pay typically runs $110,400–$165,600 across 45 roles with salary data.

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View all roles at Medtronic

At a glance

TL;DR · Senior Pre-Market Supplier Quality Engineer

Sr. Pre-Market Supplier Quality Engineer (CV CRHF) As a member of the Cardiac Ablation Solutions team, you will partner with Design, Reliability, and Technical Sourcing to develop, qualify, and commercially release cost-effective components and materials for medical devices. You will drive multi-faceted development, qualification, and validation efforts with suppliers while managing the lifecycle from acquisition through manufacturing. Your daily responsibilities include performing statistical data analysis using Minitab and MS Excel, conducting Gage R&R studies, and authoring characterization documentation to ensure compliance with GMP and ISO 13485 standards. You will also manage supplier audits, negotiate Quality Agreements, and resolve complex technical issues using methods like DMAIC or Fishbone. This role focuses on the critical domain of arrhythmia management, ensuring that high-quality components are engineered for reliability and manufacturability to support life-saving cardiac mapping and ablation technologies.

What you'll do

  • Identify, develop, qualify, and commercially release cost-effective components and materials for new product development.
  • Partner with Technical Sourcing to evaluate and approve new suppliers based on business, quality, and technical requirements.
  • Monitor parts through the manufacturing cycle and resolve supplier-related problems as they occur.
  • Lead the resolution of complex issues regarding supplied components using corrective and preventive action processes.
  • Develop and manage a regular audit schedule to ensure suppliers meet Good Manufacturing Practices (GMP) and quality standards.
  • Perform statistical data analysis on component qualification data using Minitab and MS Excel.
  • Author technical documentation for material characterization, qualification, and product acceptance.
  • Negotiate Quality Agreements with suppliers and develop inspection tooling and test methods for new components.

What we're looking for

  • Bachelor’s degree in Engineering, Science, or a technical field with 4+ years of experience in Engineering and/or Quality.
  • Advanced degree in Engineering, Science, or a technical field with 2+ years of experience in Engineering and/or Quality.
  • Preferred 2+ years of supplier quality engineering experience in the medical device industry or related field.
  • Knowledge of PPAP process and advanced knowledge of statistics and DOE execution.
  • ASQ CQE certification or ASQ Lead auditor certification is preferred.
  • Familiarity with manufacturing processes, R&D, and contract manufacturing qualification.
  • Proficiency in MS Office tools including Minitab, Word, Excel, PowerPoint, and Project.
  • Work Authorization &amp.

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