Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$72к-94к/год
$84к$92кмедиана$110к
По похожим ролям (49) ~ $92к/год
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Понятная стартовая роль в компании-разработчике медицинских изделий: есть практическая инженерная работа с процессами и валидацией, но важно учитывать работу на месте и условия чистых помещений.
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Работа на производствеЧёткие задачиМедицинские технологииХорошие льготы
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Manufacturing Engineer I (Medical Devices) (Manufacturing/Medical Devices): Developing and improving manufacturing processes, tooling, equipment, and documentation for medical device production with an accent on root cause analysis, process validation, quality systems, and production efficiency. Focus on designing fixtures, qualifying equipment, optimizing processes with statistical techniques, and coordinating cross-functional engineering and supplier activities.
Location: Roseville, CA, United States; onsite work required
Annual base salary: $72,000–$94,000
Company
hirify.global is a global healthcare company that designs, develops, manufactures, and markets medical products for challenging medical conditions.
What you will do
Solve manufacturing problems, perform root cause analysis, and implement validated process improvements.
Support production by maintaining product and process documentation and improving yield, efficiency, and throughput.
Design fixtures, source tooling and equipment, implement production-line fixturing, and perform equipment qualifications.
Test and validate processes, equipment, raw materials, and products; author protocols, reports, conclusions, and recommendations.
Plan and coordinate engineering project phases, develop product and process specifications, and optimize processes using statistical techniques.
Coordinate with suppliers, train assemblers, quality control staff, and technicians, and support compliance with quality systems.
Requirements
Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering, a related degree, or an equivalent combination of education and experience.
Excellent written, verbal, and interpersonal communication skills are required.
Proficiency in Word, Excel, PowerPoint, Access, and other computer applications is required.
Ability to work in office, laboratory, and clean room environments and willingness and ability to work onsite.
Ability to lift and move up to 25 pounds, move between buildings and floors, remain stationary and use standard office equipment for extended periods, and access cabinets or supplies as needed.
Ability to read, prepare emails, produce documents and spreadsheets, and communicate accurate information with employees at all levels.
Ability to adhere to the Company’s Quality Management System, applicable domestic and global quality regulations, standards, procedures, and security, privacy, and compliance requirements.
Nice to have
1+ year of relevant engineering experience.
Engineering experience in a manufacturing environment.
Medical device industry experience.
Knowledge of FDA regulations, Lean/Flow Manufacturing, materials, and manufacturing processes.
Culture & Benefits
Collaborative teamwork environment with continuous learning and performance recognition.
Benefits for eligible employees include medical, dental, vision, life, AD&D, short- and long-term disability insurance, and a 401(k) with employer match.
Paid parental leave, eleven paid company holidays, at least fifteen days of accrued vacation per year with increases based on tenure, and paid sick time in accordance with applicable laws.
Work may involve laboratory and clean room conditions and potential exposure to blood-borne pathogens.
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