Sr Quality Engineer - Plymouth, Mn

Medtronic

Plymouth, Mn, USA
Base: $96,800.00 - $145,200.00; bonus/equity: mip;...
Onsite
Quality standards and protocol
Inspecting, testing and evaluating
Statistical analysis
Medtronic is seeking a Senior Quality Engineer for their Plymouth, MN location. The role involves leading quality assurance processes and collaborating with cross-functional teams to ensure product excellence, particularly in the medical device industry

Job Summary

  • At Medtronic, quality is at the heart of everything we do—it’s how we fulfill our Mission to alleviate pain, restore health, and extend life.
  • As a Quality Engineer II at our Nathan Lane Manufacturing site, you will be at the forefront of driving excellence in our products and processes.
  • Medtronic offers a competitive Salary and flexible Benefits Package.

Matching Summary

Match Score: 85

Medtronic is seeking a Senior Quality Engineer for their Plymouth, MN location. The role involves leading quality assurance processes and collaborating with cross-functional teams to ensure product excellence, particularly in the medical device industry.

Salary

Base: $96,800.00 - $145,200.00; Bonus/Equity: MIP; Benefits: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, Simple Steps, Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement, Capital Accumulation Plan

Skills & Requirements

Must-have

  • quality standards and protocol
  • inspecting, testing and evaluating
  • statistical analysis
  • corrective measures
  • production equipment

Nice-to-have

  • strong written and verbal communication
  • strong critical thinking
  • analytical skills
  • CAPA knowledge
  • belonging

Key Requirements

  • Bachelor’s Degree in Engineering, Science or technical field with 4+ years of work experience
  • Master’s Degree in Engineering, Science or technical field with 2+ years of work experience
  • PhD in Engineering, Science or technical field with 0+ years of work experience
  • Previous experience in medical device
  • Previous process validation experience
  • Previous experience with Test Method Validations
  • Previous experience with Master Validation Records and Risk Management documentation

Work Rights

Unrestricted US work authorization required for roles below Principal level

Sponsorship: available

Tailored Resume

Cover Letter