обновлено 10 дней назад
Program Manager, Engineering-2 (Medical Devices)
137 000 - 202 000$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Program Manager, Engineering-2 (Medical Devices): Managing multiple engineering and product development projects from inception through implementation and handoff with an accent on regulated product environments, financial control, quality systems, and cross-functional execution. Focus on governing schedules and milestones, resolving project risks and scope changes, coordinating FDA and ISO-related requirements, and supporting manufacturing transfer and technical development.
Location: Plymouth, Minnesota, United States. The role requires domestic and international travel of up to 30% at times, including possible visits to customer and supplier sites.
Salary: $137,000–$202,000 per year, plus a cash-based incentive program.
Company
develops regulated products and engineering solutions, including medical components, subassemblies, and finished medical devices.
What you will do
- Manage multiple engineering and product development projects from inception through implementation and handoff.
- Maintain project plans, quotes, budgets, specifications, schedules, milestones, forecasts, and financial tracking in Oracle ERP.
- Lead cross-functional project and program teams across engineering, marketing, quality, regulatory, design assurance, and manufacturing.
- Serve as the primary escalation point, provide project updates, and manage issues, risks, scope changes, customer agreements, billing events, and milestones.
- Support commercial opportunities and quote development, including technical capability and project requirement assessments.
- Improve PMO tools and processes, apply product development and manufacturing transfer systems, and mentor team members or manage up to 2–3 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.
- At least 7 years of experience, including 4 years in a regulated product environment and 3 years leading multiple projects and project teams.
- Knowledge of FDA, ISO, MDD, and related quality and regulatory requirements connected to design controls and product development.
- Experience with product and process development engineering principles and manufacturing processes across multiple products.
- Strong leadership, coaching, critical-thinking, problem-solving, communication, presentation, organization, collaboration, and conflict-resolution skills.
- Ability to travel domestically and internationally, up to 30% at times.
Culture & Benefits
- Values-driven culture focused 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.
- 401(k) plan with company matching contributions and optional supplemental insurance programs.
- 80 hours of company-designated holidays and annual paid time off.
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