Quality-Focused Engineering Program Manager (NPD)

Medtronic plc

Jacksonville (FL)

Vor Ort

USD 142.000 - 214.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

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Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Benefits dieser Stelle

Competitive salary
Benefits package

Zusammenfassung

Medtronic plc, based in Jacksonville, Florida, is seeking an Engineering Program Manager to act as the Voice of Quality across New Product Development programs. The role leads quality and reliability strategies, partnering with engineering, manufacturing, supplier quality, regulatory, and business stakeholders from concept through commercialization and post-market transition.

The position is onsite in Jacksonville with travel under 10% and requires strong experience in quality systems, risk

Qualifikationen

  • Experience leading cross-functional product development or quality programs.
  • Experience applying risk management, quality, and reliability methodologies in regulated product development environments.
  • Experience with quality systems, design controls, and product lifecycle management processes.

Aufgaben

  • Lead quality and reliability strategy, plans, metrics, and risk management activities for assigned new product development programs.
  • Manage execution across extended quality functions, including design quality, software quality, supplier quality, manufacturing quality, and reliability engineering teams.
  • Represent the Voice of Quality on cross-functional core teams and serve as the final quality authority for assigned projects.
  • Drive DRM, DfR, FTQ, and defect prevention initiatives throughout product development.
  • Identify quality and reliability risks, implement risk reduction strategies, and lead root cause investigations and corrective and preventive actions.
  • Partner with suppliers and manufacturing sites to evaluate quality risks, support sourcing decisions, and ensure readiness for product launch and lifecycle management.
  • Lead compliance planning, assessments, audit support activities, and adherence to quality system and regulatory requirements.
  • Support key development deliverables including DHF, DMR, PPAP, regulatory submissions, software lifecycle documentation, and product transfer activities.

Kenntnisse

Cross-functional leadership
Quality strategy
Regulatory knowledge

Ausbildung

Bachelor's degree in Engineering or related field
Master's degree (preferred)

Tools

DRM
DfR
PPAP
FDA 21 CFR 11

Jobbeschreibung

Medtronic plc, based in Jacksonville, Florida, is seeking an Engineering Program Manager to act as the Voice of Quality across New Product Development programs. The role leads quality and reliability strategies, partnering with engineering, manufacturing, supplier quality, regulatory, and business stakeholders from concept through commercialization and post-market transition.

The position is onsite in Jacksonville with travel under 10% and requires strong experience in quality systems, risk

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