Principal Quality Engineer - North Haven, Ct

Medtronic UK

North Haven, United States
Base: $119,200.00 - $178,800.00; bonus/equity: eli...
Onsite
Product reliability
Optimize processes
Regulatory compliance
We are seeking a Principal Quality Engineer to join our team in North Haven, CT, integral to ensuring the highest standards of quality and compliance in our medical device manufacturing processes

Job Summary

  • We are seeking a Principal Quality Engineer to join our team in North Haven, CT, integral to ensuring the highest standards of quality and compliance in our medical device manufacturing processes.
  • Responsibilities include developing, modifying, applying, and maintaining quality standards and protocols, collaborating with engineering and manufacturing, and devising inspection and testing methods.
  • Medtronic offers a competitive Salary and flexible Benefits Package, including health, dental, vision insurance, 401(k) with employer match, and incentive plans.

Matching Summary

We are seeking a Principal Quality Engineer to join our team in North Haven, CT, integral to ensuring the highest standards of quality and compliance in our medical device manufacturing processes.

Salary

Base: $119,200.00 - $178,800.00; Bonus/Equity: Eligible for Medtronic Incentive Plan; Benefits: Health, Dental, Vision, HSA, FSA, Life Insurance, LTD, Daycare FSA, Tuition Assistance, Simple Steps, 401(k), PTO, Holidays, ESPP, EAP, Non-qualified Retirement Plan Supplement

Skills & Requirements

Must-have

  • product reliability
  • optimize processes
  • regulatory compliance
  • root cause investigations
  • statistical analysis
  • FDA-regulated environments

Nice-to-have

  • champion healthcare access
  • foster belonging
  • engineering the extraordinary
  • technical leadership
  • mentor and coach teams

Key Requirements

  • Baccalaureate degree and 7 years relevant experience OR Master's degree and 5 years relevant experience OR PhD and 3 years relevant experience
  • Subject Matter Expert in process validation
  • Experience leading advanced root cause investigations
  • Advanced proficiency in statistical analysis
  • Ability to mentor, coach, and influence teams
  • Strong working knowledge of Minitab
  • Expert ability to read engineering drawings
  • Significant experience in FDA-regulated environments

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter