requirements managementproject managementproduct developmentmanufacturingchange managementconfiguration managementbill of materialsmedical devices
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
развернуть
$124к-212к/год
$120к$150кмедиана$170к
По похожим ролям (49) ~ $150к/год
На СНГ рынке: $4.4к/мес ($2.4к - $5.7к)
85
Отличная вакансия
развернуть
Это четко структурированная и стабильная позиция в профильной продуктовой компании в сфере медтеха с понятными обязанностями и прозрачной системой компенсации.
Четкие обязанности
Стабильная отрасль
?Офисный формат
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Product Project Management Specialist (Medical Devices): Managing cross-functional projects for new product development and lifecycle management of diabetes pumps and app manager systems with an accent on configuration management, requirements planning, and manufacturing change orders. Focus on coordinating product delivery, resolving project issues, and maintaining Bills of Materials and implementation processes across domestic and international manufacturing sites.
Location: Full time on-site in Northridge, California, United States. The role may require 15–20% domestic and international travel.
Salary: $124,000–$212,000 USD annually for the California location.
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
Lead or leverage cross-functional teams to evaluate, develop, and manage new product development and product lifecycle projects.
Manage project operations, schedules, status reporting, delivery activities, and communication between project teams, planning, line management, and stakeholders.
Manage product and service development and implementation across departmental and cross-functional teams.
Assess project issues, develop resolutions, and establish mechanisms for progress monitoring, intervention, and problem solving.
Gather, plan, elicit, and manage requirements to address key stakeholder needs and secure stakeholder engagement.
Own Bills of Materials and associated change orders for transfer and implementation to manufacturing sites.
Requirements
Bachelor’s degree and a minimum of 4 years of relevant experience, or an advanced degree and a minimum of 2 years of relevant experience.
Ability to work independently, interact with computers, and communicate with peers and co-workers.
Nice to have
Experience with medical device regulations and management.
Strong attention to detail and ability to understand complex requirements and confirm design compliance.
Problem-solving ability and readiness to think outside the box.
Culture & Benefits
Full-time employee position with competitive compensation and flexible benefits.
Health, dental, and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, 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, Employee Assistance Program, and additional retirement and capital accumulation plans for eligible employees.
Equal employment opportunity and reasonable accommodations for qualified individuals with disabilities.
Будьте осторожны
Если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого. Это мошенники. Обязательно жмите «Пожаловаться» или пишите в поддержку. Подробнее в гайде →