4 дня назад
Senior Engineering Program Manager (Medtech)
171 200 - 256 800$
Мэтч & Сопровод
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Описание вакансии
Текст:
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 Incentive Plan.
Company
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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