Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Мало
$133к-200к/год
$150к$170кмедиана$190к
По похожим ролям (49) ~ $170к/год
74
Хорошая вакансия
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Роль четко описана и дает большую ответственность в производстве медицинских устройств, но зарплата ниже медианы рынка, а работа только на месте и поездки до 30% могут быть неудобны.
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Ниже рынкаРабота на местеПонятная зона ответственностиМедицинские технологии
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Sr Technical Program Manager, Automated Equipment (Automation/Manufacturing): Leading complex automation and capital equipment programs from concept through design, build, validation, and production deployment with an accent on supplier management, technical reviews, risk mitigation, and manufacturing readiness. Focus on delivering multi-million-dollar equipment programs across global manufacturing operations, coordinating cross-functional engineering teams, and ensuring performance, safety, quality, schedule, and budget compliance.
Location: On-site at the Acton, Massachusetts manufacturing, development, and laboratory facilities; domestic and international travel up to 30% may be required.
Annual base salary: $133,400–$200,075 USD for U.S.-based positions. Incentive compensation may also be available.
Company
hirify.global is a medical device company developing the Omnipod wearable insulin delivery platform and related drug-delivery technologies for people with diabetes and other conditions.
What you will do
Lead large-scale automation and capital equipment programs from capital approval through production deployment.
Own technical execution, supplier relationships, schedules, budgets, risks, issue resolution, and stakeholder communications.
Translate manufacturing and business requirements into equipment specifications, project plans, milestones, and reporting.
Review equipment designs and lead technical assessments covering performance, reliability, safety, quality, and manufacturability.
Lead supplier reviews, FAT, SAT, commissioning, validation, and production-readiness activities.
Coordinate Mechanical Engineering, Controls Engineering, Manufacturing Engineering, Quality, Validation, Operations, and leadership stakeholders across global manufacturing sites.
Requirements
Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, or a related technical discipline with 8+ years of relevant experience, or a master’s degree with 6+ years of experience.
Experience leading automation, capital equipment, manufacturing engineering, or industrial automation projects from concept through production deployment.
Strong knowledge of automation equipment, manufacturing systems, robotics, controls, machine safety, and industrial engineering.
Experience managing automation suppliers, contract machine builders, capital budgets, schedules, risks, and project financial performance.
Working knowledge of FAT, SAT, IQ/OQ/PQ, validation, and regulatory requirements, preferably in regulated or medical device manufacturing.
Ability to work on-site in Acton, Massachusetts, on manufacturing floors, in development laboratories, and in cleanroom environments, with the ability to lift up to 30 lbs.
Culture & Benefits
Work within a global manufacturing network focused on improving patient lives through wearable medical technology.
Medical, dental, and vision insurance.
401(k) plan with company match.
Paid time off and employee wellness programs.
Opportunities to standardize engineering practices across global automation programs.
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