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3 дня назад

Project Manager III (Medical Devices)

137 600 - 189 200$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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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