Senior Quality Program Manager - Nmph - Rice Creek/fridley, Mn (onsite)

Medtronic Diabetes

Fridley, MN, US
Base: $178,400.00 - $267,600.00; bonus: eligible f...
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7 years medical device experience
Bachelor's degree required
Capa process leadership
** Medtronic Diabetes is seeking a Senior Quality Program Manager for their Fridley, MN location. This role involves leading cross-functional teams to enhance product quality and compliance within the neuromodulation portfolio, with a focus on driving improvements and ensuring regulatory alignment. **

Job Summary

  • This role is mission-critical at the intersection of innovation and process excellence to ensure products meet global customer and regulator expectations.
  • The successful candidate will lead a high-performing team to execute compliance and product quality improvements for Neuromodulation products while presenting progress to executive leadership.
  • Medtronic offers a competitive salary range of $178,400.00 - $267,600.00 along with comprehensive benefits including health insurance, 401(k) matching, and incentive plans.

Matching Summary

Match Score: 75

** Medtronic Diabetes is seeking a Senior Quality Program Manager for their Fridley, MN location. This role involves leading cross-functional teams to enhance product quality and compliance within the neuromodulation portfolio, with a focus on driving improvements and ensuring regulatory alignment. **

Salary

Base: $178,400.00 - $267,600.00; Bonus: Eligible for Medtronic Incentive Plan (MIP); Benefits: Health, dental, vision, 401(k), PTO, tuition assistance

Skills & Requirements

Must-have

  • 7 years medical device experience
  • Bachelor's degree required
  • CAPA process leadership
  • Cross-functional program execution
  • FDA and ISO standards knowledge

Nice-to-have

  • Design controls experience
  • Six Sigma and FMEA tools
  • Regulatory inspection representation
  • Manufacturing transfer experience
  • Executive stakeholder influence

Key Requirements

  • Bachelor's degree with 7 years experience OR advanced degree with 5 years
  • Unrestricted US work authorization required
  • Experience with FDA and ISO 13485/14971 standards

Work Rights

Must have unrestricted US work authorization

Tailored Resume

Cover Letter