NPI Project Manager - Medical Devices (Hybrid)

Actalent

Big Lake (MN)

Hybrid

USD 100,000 - 140,000

Full time

18 hours ago
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Benefits offered by this job

Medical benefits
Dental benefits
Vision benefits
401(k) plan

Job summary

Actalent in Big Lake, MN is seeking a Project Manager (NPI) to lead New Product Introduction programs in a high-precision medical contract manufacturing environment. You will coordinate customers, engineering, quality, operations, and manufacturing to move programs from prototype through production, ensuring on-time delivery, budget adherence, and defined scope.

The role requires strong project leadership, excellent communication, and experience with regulated medical device environments.

Qualifications

  • 7+ years in project or program management within manufacturing.
  • Experience with NPI in medical devices or high-precision manufacturing.
  • Proven ability to manage customer-facing programs and budgets.
  • Experience leading cross-functional teams across engineering, manufacturing, and quality.

Responsibilities

  • Serve as primary customer contact and internal leader for NPI programs.
  • Transition new opportunities from quote to execution with Sales teams.
  • Lead customer interactions and manage risks, budgets, and schedules.
  • Develop and control program budgets, milestones, and design-to-cost efforts.
  • Collaborate with Engineering, Manufacturing, Supply Chain, and Quality.

Skills

Project leadership
Cross-functional collab
Stakeholder management
Customer interfacing

Education

Bachelor's degree
Master's degree
PMP certification
MBA

Tools

Microsoft Project

Job description

Actalent in Big Lake, MN is seeking a Project Manager (NPI) to lead New Product Introduction programs in a high-precision medical contract manufacturing environment. You will coordinate customers, engineering, quality, operations, and manufacturing to move programs from prototype through production, ensuring on-time delivery, budget adherence, and defined scope.

The role requires strong project leadership, excellent communication, and experience with regulated medical device environments.

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