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Program Manager, Engineering-1 (Medical Devices)

137 000 - 202 000$
Формат работы
onsite
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
Program Manager, Engineering-1 (Medical Devices): Managing end-to-end engineering and product development projects for regulated medical device programs with an accent on budgets, schedules, quality systems, and cross-functional execution. Focus on resolving project risks, coordinating manufacturing and regulatory requirements, and delivering prototypes, verification units, and production handoffs on time and within budget.

Location: Plymouth, MN, United States. The role requires domestic and international travel of up to 30% at times.

Salary: $137,000–$202,000 per year, plus a cash-based incentive program.

Company

hirify.global develops regulated products and engineering solutions, with work spanning medical components, subassemblies, finished medical devices, and related manufacturing processes.

What you will do

  • Manage multiple engineering and product development projects from initiation through implementation and handoff.
  • Maintain project plans, quotes, budgets, forecasts, specifications, schedules, milestones, and performance indicators.
  • Track project costs, revenue recognition, billing events, customer agreements, and delivery against budget and schedule.
  • Lead cross-functional coordination across engineering, manufacturing, quality, regulatory, marketing, design assurance, suppliers, and customers.
  • Resolve project issues, risks, scope changes, and escalations while providing status updates to internal and external stakeholders.
  • Support commercial opportunities and quote development, improve PMO processes, and mentor team members or direct reports.

Requirements

  • Bachelor’s degree in engineering or a related technical field preferred; a master’s degree and project/program management certification are welcomed.
  • 7+ years of experience, including at least 4 years in a regulated product environment and 3 years in project management leading multiple projects and teams.
  • Knowledge of FDA, ISO, MDD, and related quality and regulatory requirements connected to design control and product development.
  • Understanding of product and process development engineering principles and manufacturing processes across multiple products.
  • Strong leadership, coaching, critical thinking, problem-solving, communication, presentation, organization, collaboration, and conflict-resolution skills.
  • Ability to travel domestically and internationally, up to 30% at times.

Culture & Benefits

  • Values-led culture centered on customer success, innovation, collaboration, inclusion, candor, and integrity.
  • Medical, dental, vision, disability, life insurance, and adoption benefits with immediate eligibility.
  • Parental leave after one year and optional supplemental life, critical illness, hospital indemnity, and accident insurance programs.
  • Immediate eligibility for a 401(k) plan with company matching contributions.
  • 80 hours of company-designated holidays and an annual paid time off allotment.

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