Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$138к-189к/год
$120к$140кмедиана$160к
По похожим ролям (49) ~ $140к/год
На СНГ рынке: $3.5к/мес ($2.1к - $5.6к)
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Хорошая вакансия
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Чётко описанная роль в управлении проектами у известной medtech-компании, с ответственностью за межфункциональные команды и поддержкой развития; требование жить недалеко от офиса в Ирвайне ограничивает выбор места.
Привязка к офису
Понятная зона ответственности
Поддержка развития
Медицинские технологии
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Project Manager III (Medical Devices): Driving execution of new product development and sustaining programs with an accent on integrated planning, cross-functional coordination, risk management, and budget tracking. Focus on facilitating core teams, resolving schedule and resource conflicts, preparing phase-gate and PDT decisions, and maintaining program control in a regulated product development environment.
Location: Hybrid role based in Irvine, California, United States; the employee must live within commuting distance of the office.
Base salary: $137,600–$189,200 annually, plus eligibility for a variable annual bonus.
Company
hirify.global develops, manufactures, and markets research and clinical diagnostic products for the life sciences and healthcare sectors.
What you will do
Drive day-to-day execution of new product development and sustaining programs.
Develop and maintain integrated project plans, schedules, milestones, dependencies, critical paths, and VPM boards.
Lead core team and functional workstream meetings across R&D, Quality, Regulatory, Operations, and Marketing.
Resolve risks, issues, scheduling conflicts, and action items, escalating concerns to support timely leadership decisions.
Prepare phase-gate and Portfolio Decision Team materials supported by analysis of scope, budget, and resource trade-offs.
Track program spending against plan and support monthly financial reporting and forecasting.
Requirements
Bachelor’s degree in engineering, life sciences, business, or a related field.
5–8 years of project or program management experience, ideally in medical devices, diagnostics, or another regulated product development environment.
Experience managing multiple cross-functional workstreams and competing priorities in a fast-paced new product development environment.
Strong facilitation, communication, and stakeholder management skills, including the ability to present to and influence senior leadership.
Working knowledge of stage-gate or phase-gate development processes, risk management, and visual project management tools such as VPM, MS Project, Smartsheet, or similar.
Nice to have
PMP certification.
Culture & Benefits
Hybrid work arrangement with an Irvine office location.
Medical plans, HSA funds, fertility support, group life and disability coverage, paid parental leave, and 401(k) with profit sharing.
Employee stock purchase program, mental health support, pet insurance, wellness programs, paid time off, and employee resource groups.
Learning and development opportunities, education benefits, and student debt relief support.
Annual bonus eligibility based on individual objectives and company performance.
Hiring process
Bio-Rad does not accept agency resumes unless the agency has been authorized by a Bio-Rad recruiting representative.
Applicants should beware of fraudulent recruiters and job scams requesting personal or financial information.
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