1 день назад
Program Manager, Engineering (Medical Devices)
137 000 - 202 000$
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Описание вакансии
Текст:
TL;DR
Program Manager, Engineering (Medical Devices): Leading multiple product development and engineering projects from initiation through implementation and handoff, with an accent on regulated medical-device environments, financial tracking, and cross-functional execution. Focus on managing complex schedules, budgets, risks, regulatory requirements, and customer or supplier coordination across the full project lifecycle.
Location: Plymouth, Minnesota, United States
Salary: $137,000–$202,000 per year, plus a cash-based incentive program.
Company
develops regulated products and medical-device components while supporting customer and patient needs through engineering, manufacturing, quality, and regulatory capabilities.
What you will do
- Manage and execute multiple engineering and product-development projects from inception through implementation and handoff.
- Maintain project plans, schedules, quotes, budgets, ERP updates, forecasts, billing milestones, and financial tracking.
- Define key performance indicators and provide leadership, governance, status reporting, and escalation management for project and program teams.
- Coordinate cross-functional work across marketing, quality, regulatory, design assurance, manufacturing, suppliers, and customers.
- Identify and resolve project risks and issues, manage scope changes, and support commercial teams with opportunity assessment and quote development.
- Improve PMO processes and tools, share best practices, and mentor cross-functional associates and up to two or three direct reports.
Requirements
- Bachelor’s degree in engineering or a related technical field preferred; a master’s degree and accredited project/program management certification are welcomed.
- 7+ years of experience, including at least 4 years in a regulated product environment and 3 years in project management leading multiple projects and teams.
- Strong team leadership, coaching, critical thinking, problem-solving, communication, presentation, organization, collaboration, and conflict-resolution skills.
- Knowledge of FDA, ISO, MDD, and related quality and regulatory requirements connected to design controls and product development.
- Understanding of product and process development engineering principles and manufacturing processes, preferably involving medical components, subassemblies, and finished medical devices.
- Ability to travel domestically and internationally, up to 30% at times.
Culture & Benefits
- Values-driven culture centered on customer success, innovation, collaboration, inclusion, candor, and integrity.
- Medical, dental, vision, disability, life insurance, and adoption benefits with immediate eligibility.
- Parental leave available after one year and optional supplemental insurance programs.
- 401(k) plan with company matching contributions and immediate eligibility.
- 80 hours of company-designated holidays and an annual paid-time-off allotment.
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