Supplier Qual Engineer II - CST - Boxborough, MA

Medtronic

Closes in 5 days Hybrid

Quick summary

Work type
Hybrid
Location
Boxborough, MABoston, MABeverly, MABillerica, MA
Salary
$80,000–$120,000 / yr
Posted
3 days ago
Closes
Jun 20, 2026 (soon)
Nearby
99+ roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $155k
This role $100k
$66k most similar roles pay here $207k

This role pays less than 93% of similar roles. Most pay $127,500–$183,179 — the shaded band above. At the midpoint, this role pays about $100k versus about $155k for comparable roles.

Based on 239 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 54 open roles on FindRole.

Listed pay typically runs $108,800–$163,200 across 53 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · Supplier Qual Engineer II - CST - Boxborough, MA

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As a Supplier Quality Engineer II at Medtronic’s Cranial & Spinal Technologies unit, you will ensure suppliers deliver high-quality materials and components that meet regulatory standards. Your daily tasks include leading supplier qualification activities, executing risk-based audit plans, and monitoring supplier performance to maintain compliance with GMPs and quality requirements. You will collaborate closely with engineering teams on new product development projects, developing acceptance sampling strategies and control plans while supporting the validation of internal test methods. This role requires a bachelor’s degree in engineering or a technical field plus two years of relevant experience, proficiency in quality management systems like FDA Quality System Regulations and ISO 13485, and knowledge of quality engineering tools such as CAPA and FMEA.

Skills

ISO FDA Quality System Regulations ISO 13485 Good Manufacturing Practices CAPA FMEA Lean Six Sigma ASQ Design Controls Risk Management Process Validation Control Plan Development

What you'll do

  • Ensure suppliers meet high-quality standards and regulatory requirements.
  • Develop and execute risk-based audit plans for supplier compliance.
  • Monitor and resolve quality issues in supplier performance proactively.
  • Support New Product Development projects with robust supplier selection.
  • Implement strategies to prevent defects and improve supplier performance.
  • Define Receiving Inspection requirements and validate internal test methods.
  • Drive continuous improvement initiatives for purchased materials and components.

What we're looking for

  • Experience in supplier qualification and performance management within regulated industries.
  • Knowledge of quality management systems, FDA Quality System Regulations, ISO 13485, and GMP.
  • Proficiency in quality engineering tools such as CAPA, root cause analysis, FMEA, and continuous improvement practices.
  • Ability to conduct supplier assessments and audits, evaluating quality systems and driving corrective actions.
  • Experience supporting New Product Development activities including Design Controls, risk management, and control plan development.
  • ASQ certification (CQE, CSQP) or Lean Six Sigma Green Belt/Black Belt preferred.

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