„Stryker“ yra pasaulinė medicinos technologijų bendrovė, aptarnaujanti sveikatos priežiūros sektorių ir siūlanti pacientų priežiūrai bei klinikinėms operacijoms skirtus produktus. Jos asortimentą sudaro ortopediniai implantai, chirurginė įranga ir ligoninėms skirti prietaisai, o veikla vykdoma Amerikoje, Azijos ir Ramiojo vandenyno regione, Europoje, Artimuosiuose Rytuose ir Afrikoje. Bendrovė kuria ir tiekia sveikatos priežiūros sprendimus įvairioms rinkoms, daugiausia dėmesio skirdama pacientų gydymo rezultatų ir sveikatos priežiūros efektyvumo gerinimui.
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.
Jungtinės Valstijos
Arizona135 600 $ – 225 900 $ / metai
Darbas vietojeVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųInžinerijos vadovasAprašymas
- 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.
Reikalavimai
- 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.
Privalumai
- Onsite work arrangement.
- Opportunity for 10% travel.