data analysisfailure analysisroot cause analysismedical devicesdesign of experimentsbiomedical engineeringelectrochemical sensorscontinuous glucose monitoring
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$97к-165к/год
$130к$140кмедиана$170к
По похожим ролям (50) ~ $140к/год
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Чётко очерченная senior-позиция в R&D продуктовой компании предлагает практическую работу над новым поколением систем мониторинга глюкозы, с подробными обязанностями и взаимодействием разных команд.
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Понятные задачиЗначимая областьШирокий соцпакетРабота на месте
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Biomedical Engineer (Medical Devices): Supporting next-generation continuous glucose monitoring products and sustaining R&D through failure analysis of complex microfabricated electrochemical biosensors with an accent on root-cause investigation, product reliability, and continuous improvement. Focus on developing analytical and test methodologies, conducting hands-on laboratory work, interpreting failure data, and implementing corrective actions across product development phases.
Location: Northridge, California, United States of America. Workplace type: On-site.
Salary: $97,000–$165,000 USD annually for roles located in California.
Company
hirify.global is a full-stack insulin delivery company developing intelligent dosing systems, predictive insights, and support for people living with diabetes.
What you will do
Support the development of next-generation continuous glucose monitoring products and sustaining R&D activities.
Lead failure analysis across sensor product development phases, including troubleshooting complex microfabricated electrochemical biosensors and identifying root causes and failure mechanisms.
Develop, document, and perform failure analyses; write formal reports and communicate findings to submitters and broader audiences.
Work with R&D, quality, regulatory, reliability, clinical, technicians, and other engineering teams to improve product quality, reliability, manufacturability, and functionality.
Develop test methodologies, analytical methods, and equipment capabilities for current and future technologies.
Conduct hands-on laboratory work, interpret data from testing and complaint repositories, define analysis strategies, and recommend and implement corrective actions.
Requirements
Bachelor’s degree and at least 4 years of relevant experience, or an advanced degree and at least 2 years of relevant experience.
Ability to perform failure analysis and root-cause investigations for complex systems and components.
Ability to conduct hands-on laboratory work and develop test or analytical methodologies.
Ability to interpret formal test, complaint-handling, and other technical data.
Ability to collaborate with R&D, quality, regulatory, reliability, clinical, technician, and engineering teams.
Nice to have
Master of Science degree in Biomedical Engineering, Chemical Engineering, or a related engineering field with 5+ years of professional experience.
Medical device industry experience.
Experience in product design and development in an R&D environment.
Experience with mechanical and/or electrochemical systems.
Direct experience with characterization, design of experiments, and data analysis methodologies, including T-tests, ANOVA, and significance testing.
Knowledge of in-vitro and in-vivo testing of subcutaneous medical devices.
Culture & Benefits
Full-time employment with competitive compensation and flexible benefits.
Health, dental, and vision insurance, plus Health Savings Account and Healthcare Flexible Spending Account access.
Life insurance, disability coverage, dependent daycare spending account, paid time off, and holidays.
401(k) plan with company match, incentive plans, Employee Stock Purchase Plan, and Employee Assistance Program.
Eligibility for additional retirement and capital accumulation plans may apply, subject to requirements.
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