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4 дня назад

Senior Engineering Program Manager (Medtech)

171 200 - 256 800$
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
Senior Engineering Program Manager (Medtech): Leading quality strategy and execution for a next-generation renal denervation medical device platform with an accent on product development planning, risk management, and regulatory-quality alignment. Focus on coordinating complex cross-functional engineering workstreams, driving design verification and design transfer, and resolving high-risk quality issues in a regulated healthcare environment.

Location: On-site four days per week at the Mounds View, Minnesota campus, United States, with less than 10% travel. Candidates must have unrestricted U.S. work authorization at hire and throughout employment.

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

Company

hirify.global develops medical technologies designed to alleviate pain, restore health, and extend life, serving patients worldwide.

What you will do

  • Lead quality strategy and planning for a high-priority renal denervation product development program.
  • Translate product development milestones into integrated workstreams, timelines, dependencies, risk plans, and resource requirements.
  • Represent Quality on a cross-functional core team spanning systems, software, hardware, mechanical engineering, clinical, regulatory, manufacturing, and supply chain.
  • Drive quality-owned deliverables including risk management, design verification, and design transfer.
  • Monitor quality metrics and risk indicators, communicate progress, and lead mitigation planning.
  • Influence technical and leadership decisions through clear communication of priorities, risks, and outcomes.

Requirements

  • Unrestricted U.S. work authorization is required; sponsorship is not available for roles below Principal level.
  • Bachelor’s degree in science, technology, engineering, or mathematics with at least 7 years of technical experience, or an advanced STEM degree with at least 5 years of technical experience.
  • Experience leading quality planning and execution within complex product development programs.
  • Strong understanding of system-level product development integrating software, hardware, mechanical design, and clinical or user needs.
  • Ability to lead through influence across engineering, quality, regulatory, clinical, manufacturing, and supply chain functions.
  • Experience working in regulated medical device or similarly controlled environments.

Nice to have

  • Success leading complex cross-functional product development initiatives from strategy through execution.
  • Experience collaborating with geographically distributed teams and multiple leadership levels.
  • Experience resolving high-risk quality issues through root cause analysis and risk-based mitigation.

Culture & Benefits

  • Purpose-driven work focused on improving patient outcomes and advancing healthcare technology.
  • Inclusive environment supporting diverse cultures, genders, and perspectives.
  • Health, dental, vision, life, disability, and spending account benefits for eligible regular employees.
  • 401(k) plan with employer contribution and match, paid time off, paid holidays, and employee stock purchase plan.
  • Tuition assistance, employee assistance resources, wellness support, and incentive plans.

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