Stryker
Stryker
Stryker este o companie globală de tehnologie medicală care deservește sectorul sănătății prin produse concepute pentru a sprijini îngrijirea pacienților și operațiunile clinice. Portofoliul său include implanturi ortopedice, echipamente chirurgicale și dispozitive pentru spitale, iar activitatea companiei se desfășoară în Americi, Asia-Pacific, Europa, precum și în Orientul Mijlociu și Africa. Compania dezvoltă și furnizează soluții de sănătate pentru piețe diverse, concentrându-se pe îmbunătățirea rezultatelor pentru pacienți și a eficienței serviciilor medicale.

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.

Descriere

  • 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.

Cerințe

  • 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.

Beneficii

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

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