Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Выше рынка
$140к-175к/год
$120к$140кмедиана$160к
По похожим ролям (50) ~ $140к/год
На СНГ рынке: $3.5к/мес ($2.2к - $5.6к)
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Хорошая вакансия
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Чётко описанная руководящая роль в разработке медицинских устройств предлагает зарплату выше рыночного ориентира и хорошие льготы, но обязательное присутствие в офисе четыре дня в неделю снижает гибкость.
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Часто в офисеВыше рынкаПонятные задачиПольза для здоровьяХорошие льготы
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Sr Project Manager R&D; PMO (Medical Devices): Leading cross-functional teams through the development and commercialization of new healthcare products with an accent on integrated business planning, regulatory compliance, and market-aligned launches. Focus on managing complex schedules, budgets, ROI targets, risk, resource allocation, and continuous improvement across the product development lifecycle.
Location: Hybrid in Libertyville, Illinois, US; office attendance required at least 4 days per week
Salary: $140,000–$175,000 yearly, plus eligibility for the hirify.global Corporate Bonus Plan
Company
hirify.global is an independent, employee-owned healthcare products company developing, manufacturing, and marketing ostomy care, continence care, and critical care products worldwide.
What you will do
Lead cross-functional core teams through product development and commercialization.
Develop integrated business and commercialization plans for global product launches.
Manage project schedules, budgets, compliance requirements, and ROI targets.
Partner with functional leaders and stakeholders to support strategic decisions and resource planning.
Mentor project managers, core team leaders, and project team members.
Drive project management best practices, process adherence, and continuous improvement.
Requirements
Bachelor’s degree and 8–12 years of related experience.
8–10 years of experience managing complex product development projects, preferably in medical devices.
At least 5 years of experience leading projects or cross-functional teams.
Experience with product development, commercialization, enterprise-level processes, risk management, and quality systems.
Knowledge of 21 CFR, QSR 830, ISO 13485, and ISO 14971 regulatory requirements.
Experience working in matrixed environments with multiple stakeholder groups.
Nice to have
Master’s degree in a relevant field such as engineering, MS, or MBA.
PMP certification.
Culture & Benefits
Employee-owned organization focused on innovative healthcare products and patient dignity.
Paid parental and caregiver leave, statutory leave programs, and paid time off.
401(k) retirement savings plan with auto-enrollment, Roth option, vesting, and eligible matching contributions.
Education assistance, adoption assistance, wellness programs, and recognition programs.
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