Gpdp Project Manager

KARL STORZ SE & Co. KG

Stafford, TX, US
On-site
Lead end-to-end project execution
Manage schedules, risks, dependencies, cost targets
Drive cross-functional workstreams
KARL STORZ SE & Co. KG is seeking a GPDP Project Manager to lead innovative operating room integration projects in Stafford, TX. The ideal candidate should have extensive experience in managing complex hardware and software development projects while thriving in cross-functional team environments

Job Summary

  • This role gives you the stage and the authority to lead breakthrough innovation in the operating room.
  • You will be the single owner of delivery—the person who brings clarity, momentum, and structure to a multi‑disciplinary global team.
  • Your work directly shapes the products surgeons rely on every day.

Matching Summary

Match Score: 85

KARL STORZ SE & Co. KG is seeking a GPDP Project Manager to lead innovative operating room integration projects in Stafford, TX. The ideal candidate should have extensive experience in managing complex hardware and software development projects while thriving in cross-functional team environments.

Skills & Requirements

Must-have

  • Lead end-to-end project execution
  • Manage schedules, risks, dependencies, cost targets
  • Drive cross-functional workstreams
  • Oversee engineering deliverables
  • Ensure compliance with GPDP, QMS, regulatory

Nice-to-have

  • Thrive on orchestrating cross-functional teams
  • Simplify complexity and deliver high-impact products
  • Harnessing cutting-edge technology and precise workmanship

Key Requirements

  • 5–7+ years managing complex hardware + software development projects
  • Bachelor’s in engineering or equivalent technical PM experience
  • Experience with GPDP/stage‑gate + Agile environments
  • Strong understanding of integrated systems and engineering lifecycles
  • Excellent communication, leadership, and cross‑functional coordination
  • 8–10+ years experience in PM or engineering (Preferred)
  • PMP/IPMA/Agile certification (Preferred)
  • Medical device or regulated development experience (Preferred)
  • Experience leading global engineering teams (Preferred)

Work Rights

Not specified

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