aiquality systemsroot cause analysisvision systemsstatistical process controlprocess validationmedical device manufacturingmanufacturing process optimization
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$121к-205к/год
$130к$150кмедиана$170к
По похожим ролям (50) ~ $150к/год
На СНГ рынке: $2.5к/мес ($1.9к - $3.1к)
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Зона ответственности четко описана: разработка и валидация систем технического зрения для производства медицинских устройств с заметным влиянием на продукт; при этом нужно учитывать работу на площадке и частые командировки.
Частые поездки
Полная ответственность
Влияние на медицину
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Vision Systems Engineer (Medical Devices): Designing, implementing, validating, and optimizing vision inspection systems for medical device manufacturing lines with an accent on FDA/ISO-compliant qualification, inspection performance, and production efficiency. Focus on troubleshooting complex system failures, driving root cause analysis, improving yield and throughput, and integrating vision requirements with manufacturing processes.
Location: Full-time on-site in Northridge, California, United States; business travel required 25–40% depending on project needs.
Salary: $121,000–$205,000 USD annually for California roles.
Company
hirify.global is a full-stack insulin delivery company developing intelligent dosing systems, predictive insights, and support solutions for people living with diabetes.
What you will do
Own the design, implementation, validation, and optimization of vision inspection systems across manufacturing lines.
Design manufacturing processes, production layouts, equipment arrangements, operating sequences, and material-handling procedures.
Lead process development, qualification, and validation of vision inspection systems, including IQ/OQ/PQ, in compliance with FDA and ISO regulations.
Define vision system requirements, acceptance criteria, and performance metrics with R&D, Quality, and Contract Manufacturing partners.
Troubleshoot complex vision system failures, perform root cause analysis, and implement sustainable corrective actions.
Drive continuous improvement in yield, scrap reduction, cycle time, capacity, throughput, efficiency, and overall equipment effectiveness using manufacturing performance metrics.
Requirements
Bachelor’s degree and at least 7 years of relevant experience, or an advanced degree and at least 5 years of relevant experience.
Experience in medical device manufacturing, process validation, quality systems, and regulatory requirements.
Experience developing test methods and qualifying vision system recipes.
Experience with root cause analysis, statistical methods, and manufacturing process optimization.
Nice to have
Experience owning technical strategy, operational performance, and long-term production process optimization.
Experience integrating Manufacturing Execution Systems with vision systems.
Familiarity with GD&T and optical measurement principles.
Experience supporting Contract Manufacturers in a medical device environment.
Knowledge of machine learning or AI-based vision inspection technologies.
Six Sigma Green Belt or Black Belt certification.
Culture & Benefits
Full-time employment with a competitive compensation and flexible benefits package.
Health, dental, and vision insurance, plus Health Savings Account and Healthcare Flexible Spending Account access.
Life insurance, long-term and short-term disability coverage, paid time off, and holidays.
401(k) plan with company match, Employee Stock Purchase Plan, Employee Assistance Program, and other retirement benefits subject to eligibility.
Regular employees working at least 20 hours per week are eligible for the benefits package; some benefits may not apply to Puerto Rico employees.
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