5 дней назад
Engineer II, Process (Medical Technology)
90 000 - 120 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Engineer II, Process (Medical Technology): Developing, validating, and optimizing manufacturing processes and equipment for medical monitoring products with an accent on process capability, quality, efficiency, and manufacturability. Focus on scaling new products, investigating manufacturing issues through root cause analysis, and implementing corrective actions and continuous improvements.
Location: On-site in Irvine, California, United States
Annual salary: $90,000–$120,000, plus potential 10% bonus/incentive pay
Company
Masimo, a operating company, develops medical monitoring technologies, sensors, patient monitors, and connectivity solutions.
What you will do
- Develop, implement, and optimize manufacturing processes, methods, tooling, fixtures, and equipment.
- Support new product introduction, process scale-up, manufacturability assessment, and production readiness.
- Investigate manufacturing and process issues, perform root cause analysis, and implement corrective and preventive actions.
- Drive continuous improvement and cost reduction across yield, cycle time, scrap, labor efficiency, equipment utilization, and process performance.
- Collaborate with Quality, Manufacturing, and other engineering teams while maintaining applicable quality and regulatory requirements.
Requirements
- 3+ years of relevant process, manufacturing, or related engineering experience, preferably in a regulated manufacturing environment.
- Bachelor’s degree in Mechanical, Manufacturing, Industrial, Biomedical, Electrical Engineering, or a related technical discipline.
- Experience with manufacturing process development, process improvement, validation, or production support.
- Working knowledge of statistical process control, process capability, root cause analysis, and structured problem-solving methods.
- Ability to work on-site in Irvine, California.
Nice to have
- Experience in medical devices, life sciences, or another highly regulated manufacturing industry.
- Experience with new product introduction, manufacturing transfer, or production scale-up.
- Experience with electromechanical or optical products, process automation, equipment qualification, tooling, or fixtures.
- Knowledge of FDA Quality System requirements, ISO 13485, Lean/Six Sigma, DOE, or DFM/DFA methodologies.
Culture & Benefits
- Health care, paid time off, and medical, dental, and vision insurance for eligible employees.
- 401(k) benefits for eligible employees.
- Participation in ’s continuous improvement system.
- Equal opportunity employment and reasonable accommodation support.
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