Global PMO Director, Medical Devices & Growth

Cirtec Medical

Brooklyn Park (MN)

On-site

USD 200,000 - 270,000

Full time

14 days+
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Job summary

Cirtec Medical seeks a Sr. PMO Director to lead the Engineering Services PMO across multiple sites, driving new product development and design-for-manufacturability. You will supervise a broad program management and engineering team, shaping roadmaps, budgets, and product transfers to meet customer specifications.

You will be a senior leader on the team, responsible for strategic planning, timely execution, and maintaining regulatory and quality compliance in GMP and ISO-13485 environments.

Qualifications

  • Bachelor's degree in engineering, biomedical engineering or related field.
  • 15+ years in manufacturing, product development and program management, with at least 5 years at senior leadership level.
  • Strong background in active implant fields (Neuromodulation, CRM, etc.).
  • Experience leading multi-site teams and driving organizational development.

Responsibilities

  • Drive program governance across resources, scope, timeline, risks and budget.
  • Lead complex Active Implantable projects with attention to detail and problem solving.
  • Ensure customer satisfaction and milestone adherence.
  • Manage global Engineering P&L to reach profitability goals.
  • Develop talent and ensure agile development and delivery.

Skills

Bachelor's degree
15+ years experience
Active implant field
Leadership
Budgeting
Program management
Cross-functional collaboration

Education

Advanced degree preferred

Job description

Cirtec Medical seeks a Sr. PMO Director to lead the Engineering Services PMO across multiple sites, driving new product development and design-for-manufacturability. You will supervise a broad program management and engineering team, shaping roadmaps, budgets, and product transfers to meet customer specifications.

You will be a senior leader on the team, responsible for strategic planning, timely execution, and maintaining regulatory and quality compliance in GMP and ISO-13485 environments.

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