4 дня назад
Product Development Program Director (Neuromodulation)
201 600 - 302 400$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Product Development Program Director (Neuromodulation): Leading next-generation neuromodulation systems from product definition through development, manufacturing process characterization, production ramp, and global commercialization with an accent on cross-functional execution, regulatory readiness, and clinical value. Focus on managing complex program roadmaps, budgets, risks, verification and validation activities, and commercialization challenges across Engineering, Clinical, Regulatory, Quality, Operations, and Commercial functions.
Location: Onsite in Fridley, Minnesota, United States; travel up to 20% required.
Salary: $201,600–$302,400 annually, plus incentive compensation and long-term incentive plan eligibility.
Company
develops healthcare technologies designed to alleviate pain, restore health, and extend life, with this role supporting next-generation neuromodulation therapies.
What you will do
- Lead complex cross-functional product development programs from concept through global commercialization.
- Define program strategies, roadmaps, resource plans, budgets, milestones, and delivery objectives.
- Coordinate Engineering, Clinical, Regulatory, Quality, Operations, Marketing, Finance, Reimbursement, and Commercial functions.
- Manage risks, dependencies, critical-path activities, issue resolution, and stakeholder communications.
- Oversee verification and validation, regulatory submission readiness, manufacturing process characterization, production ramp, and commercialization planning.
- Present program vision, technology capabilities, competitive positioning, workflows, and clinical value to leadership, clinicians, and key opinion leaders.
Requirements
- Bachelor’s degree in Engineering or a scientific field with at least 10 years of technical experience and 7+ years of managerial experience, or an advanced degree with at least 8 years of relevant experience and 7+ years of managerial experience.
- Experience leading complex cross-functional product development programs through development, regulatory execution, and commercialization.
- Experience managing program budgets, schedules, resources, risks, and cross-functional deliverables.
- Experience working with Clinical, Regulatory, Quality, Operations, Marketing, and Engineering functions in a regulated industry.
- Unrestricted U.S. work authorization is required at hire and throughout employment; sponsorship is offered only for Principal-level roles and above.
- For 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
- Master’s degree in Engineering or a scientific field, or an MBA.
- Experience leading software development programs using Agile methodologies and managing multiple release cycles.
- Experience with SaaS development in a regulated environment.
- Experience supporting global, matrixed teams across multiple functions and geographic regions.
- Experience in medical devices, neuromodulation, implantable technology, or highly regulated healthcare industries.
Culture & Benefits
- Onsite work environment with collaboration across global healthcare technology functions.
- Health, dental, and vision insurance, plus Health Savings and Flexible Spending Accounts.
- Paid time off, paid holidays, disability coverage, life insurance, and employee assistance programs.
- 401(k) plan with employer contribution and match, employee stock purchase plan, and retirement benefits.
- Tuition assistance, well-being resources, incentive plans, and potential long-term incentive compensation.
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