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21 час назад

Sr Engineering Program Manager (Quality)

171 200 - 256 800$
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
Sr Engineering Program Manager (Quality): Leading complex cross-functional quality improvement programs and the CardioVascular Surgery Operating Unit Quality Strategic Plan with an accent on regulated medical technology, compliance, risk management, and operational performance. Focus on coordinating matrixed teams, removing execution barriers, tracking measurable outcomes, and communicating risks and recommendations to executive leadership.

Location: Minimum four days per week onsite in Mounds View, Minnesota, or Dexter/Grand Rapids, Michigan, United States.

Salary: $171,200–$256,800 per year, plus eligibility for the hirify.global Incentive Plan.

Company

hirify.global develops healthcare technologies focused on alleviating pain, restoring health, and extending life.

What you will do

  • Lead complex quality improvement programs across the product lifecycle, manufacturing operations, supplier network, and quality management system.
  • Define program scope, objectives, timelines, resources, success criteria, and risk mitigation plans.
  • Lead matrixed teams across research and development, quality, manufacturing engineering, operations, supplier quality, and regulatory affairs.
  • Develop and execute the CardioVascular Surgery Operating Unit Quality Strategic Plan, including roadmaps, metrics, milestones, and governance.
  • Track performance, benefits realization, organizational impact, risks, and mitigation plans.
  • Prepare executive-level updates, strategic reviews, recommendations, and escalations.

Requirements

  • Bachelor's degree in engineering, quality, life sciences, business, or a related technical discipline.
  • At least 7 years of relevant experience, or at least 5 years of relevant experience in quality, engineering, operations, program management, or related functions.
  • Experience working in a regulated industry environment.
  • Unrestricted U.S. work authorization is required at hire and throughout employment; sponsorship is not available for roles below Principal level.
  • Ability to influence stakeholders and drive execution across matrixed organizations without direct authority.
  • For bachelor's degrees earned outside the United States, the degree must satisfy the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A).

Nice to have

  • Medical device, cardiovascular, or related medical technology experience.
  • PMP certification and Lean Six Sigma Black Belt, Green Belt, or equivalent certification.
  • Experience with strategic planning, quality transformation, continuous improvement, and complex cross-functional initiatives.
  • Knowledge of design assurance, design controls, operations or supplier quality, risk management, ISO 13485, or FDA QMSR.
  • Executive communication and presentation experience.

Culture & Benefits

  • Regular employee benefits include health, dental, vision, life, and disability insurance.
  • Access to a Health Savings Account, Flexible Spending Account, dependent daycare spending account, and tuition assistance.
  • 401(k) plan with employer contribution and match, paid time off, and paid holidays.
  • Incentive plans, Employee Stock Purchase Plan, Employee Assistance Program, and global well-being resources.
  • Professional growth and cross-functional collaboration through in-person work.

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