обновлено 5 дней назад
Director, Systems Engineering - ENT R&D (Medical Devices)
198 400 - 297 600$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Director, Systems Engineering - ENT R&D (Medical Devices) (Medical Devices): Leading systems engineering for complex ENT medical device platforms, including therapy delivery systems, devices, programmers, and accessories, with an accent on system architecture, requirements management, and cross-functional integration. Focus on building a high-performing engineering organization, integrating hardware, software, and firmware, and delivering reliable products in regulated environments.
Location: Jacksonville, Florida, United States; travel below 25%.
Salary: $198,400–$297,600 per year, plus short-term and annual long-term incentive plans.
Company
develops healthcare technologies, including ENT medical devices and systems for sinus, otology, head and neck, skull base, and airway care.
What you will do
- Lead, build, and scale a multidisciplinary Systems Engineering organization, including hiring, succession planning, and leadership development.
- Define ENT platform and system architecture strategy and translate clinical, scientific, and technology insights into product roadmaps.
- Own system-level requirements and architecture for therapy delivery systems, devices, programmers, and accessories.
- Lead systems engineering execution within a Core Team Model to support compliant, high-quality, and on-time product launches.
- Ensure integration across hardware, software, and firmware development partners while driving technology reuse and platform standardization.
- Establish scalable engineering processes, risk oversight, and systems engineering practices that improve quality and time to market.
Requirements
- Bachelor’s degree with 10 years of relevant experience, or a master’s degree with 8 years of relevant experience.
- At least 7 years of managerial experience.
- Strong foundation in systems engineering, ideally spanning electrical, mechanical, biomedical, and software engineering.
- Experience developing and delivering highly complex, high-reliability systems and technologies in regulated environments.
- Unrestricted U.S. work authorization is required at hire and throughout employment for roles below the Principal level.
- U.S. work authorization sponsorship is offered only for Principal-level roles and above.
Nice to have
- Medical device industry experience with Class I, II, or III regulated products.
- Leadership experience managing complex medical device technologies and product portfolios.
- Experience leading cross-functional, matrixed teams across engineering, clinical, regulatory, and commercial functions.
- Strong business acumen, executive presence, communication, quantitative, and analytical skills.
Culture & Benefits
- Mission-driven work focused on improving patient outcomes through healthcare technology.
- Health, dental, and vision insurance, plus health and dependent-care spending accounts.
- Life insurance, disability coverage, paid time off, and paid holidays.
- 401(k) plan with employer contribution and match, employee stock purchase plan, and incentive plans.
- Tuition assistance or reimbursement and global well-being resources.
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