Supplier Quality Engineer Ii

Medtronic UK

Memphis, Tennessee, United States
Base: $77,600.00 - $116,400.00; bonus/equity: mip ...
Onsite
Pre-market supplier quality engineering
New product introduction (npi) projects
Supplier qualification activities
In this role as a Supplier Quality Engineer II, you will support Pre-Market Supplier Quality Engineering activities for the CST Operating Unit

Job Summary

  • In this role as a Supplier Quality Engineer II, you will support Pre-Market Supplier Quality Engineering activities for the CST Operating Unit.
  • Supports Pre-Market Supplier Quality Engineering activities for New Product Introduction (NPI) projects, working in partnership with project teams and Post-Market Supplier Quality Teams to help deliver quality parts, materials, and services that allow Medtronic to provide customers with the highest quality and reliable products.
  • Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values.

Matching Summary

In this role as a Supplier Quality Engineer II, you will support Pre-Market Supplier Quality Engineering activities for the CST Operating Unit.

Salary

Base: $77,600.00 - $116,400.00; Bonus/Equity: MIP eligible; Benefits: Health, Dental, vision, HSA, FSA, Life insurance, LTD, Dependent daycare, Tuition assistance, Simple Steps, 401(k) match, Short-term disability, PTO, Holidays, ESPP, EAP, Non-qualified Retirement Plan Supplement, Capital Accumulation Plan

Skills & Requirements

Must-have

  • Pre-Market Supplier Quality Engineering
  • New Product Introduction (NPI) projects
  • supplier qualification activities
  • process development work with suppliers
  • supplier performance monitoring
  • Corrective Actions and Preventive Actions (CAPA)

Nice-to-have

  • continuous improvement mindset
  • collaborative, cross-functional team environment
  • inclusive culture where you can thrive
  • bold ideas forward with speed and decisiveness

Key Requirements

  • Bachelor's degree in Engineering
  • Minimum of 2 years of relevant experience
  • Familiarity with ISO 13485 or FDA 21 CFR 820
  • Strong organizational, technical writing, and communication skills

Work Rights

Unrestricted US work authorization required for roles below Principal level

Tailored Resume

Cover Letter