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Stryker
Stryker
H1B Visa SponsorConsultingHealthcareLogistics
Stryker is a global medical technology company serving the healthcare sector with products designed to support patient care and clinical operations. Its portfolio includes orthopedic implants, surgical equipment, and hospital devices, with operations spanning the Americas, Asia Pacific, Europe, and the Middle East and Africa. The company develops and delivers healthcare solutions for diverse markets, with a focus on improving patient outcomes and healthcare efficiency.
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Senior Manufacturing Engineering Manager – Medical Devices

Lead engineering teams and manufacturing operations for Stryker in Arizona. Oversee product transfers, process validation, and long-term capital and process improvements.

USUnited StatesAZArizona
$135,600 – $225,900 / year
On-siteFull-timeSeniorEnglish RequiredEngineering Manager

Description

  • Build and grow an effective engineering team, overseeing resources and performance while mentoring engineering leaders.
  • Set department goals, projects, and resource plans around business and customer priorities.
  • Deliver department initiatives on schedule.
  • Ensure compliance with quality, regulatory, company policy, and engineering standards.
  • Keep products and processes in a validated state.
  • Lead cross-functional teams to resolve issues.
  • Bring new products and processes into production.
  • Apply Lean, 5S, and innovation to improve quality, efficiency, cost, and operational performance.
  • Create and carry out strategic roadmaps covering three to five years.
  • Turn business priorities into project, process, technology, and capital plans.
  • Oversee department budgets, expenses, and capital investment needs.
  • Update leadership on department performance, projects, budgets, and operations.
  • Complete additional duties assigned by the manager or director.

Requirements

  • Bachelor’s degree in biomedical, chemical, electrical, industrial, mechanical, or a related engineering field.
  • At least eight years of relevant manufacturing engineering experience.
  • At least five years in a supervisory or management position.
  • Project management experience, preferably leading cross-functional initiatives.
  • Ability to build, develop, and engage high-performing technical teams.
  • Ability to lead cross-functional problem solving.
  • Experience applying engineering rigor in regulated medical device manufacturing.
  • Experience with risk analysis, problem solving, process validation, and Design for Manufacturing.
  • Ability to develop and execute strategic roadmaps spanning three to five years.
  • Master’s degree or MBA preferred.

Benefits

  • Onsite work arrangement.
  • Opportunity for 10% travel.

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