Project Manager- MedTech


Tuttlingen
Contract
Negotiable
Manufacturing
CR/595055_1780407705
Project Manager- MedTech

Project Manager - MedTech Migration Project (MDD → MDR)

Location: Germany (Flexible / Hybrid)
Start Date: ASAP (within 2 weeks)
Contract Type: Freelance / Interim (6 months)


Overview

We are seeking an experienced Project / Program Manager to lead the Physical Migration workstream within a global MDD to MDR transition program.

This role is critical to ensuring uninterrupted product supply and a seamless transition across manufacturing, supply chain, and regulatory interfaces.

The ideal candidate will bring strong cross-functional leadership, deep operational understanding, and the ability to drive complex transformation initiatives in a fast-paced environment.


Key Objectives

  • Lead the end-to-end Physical Migration workstream within the MDD → MDR transition
  • Ensure execution across manufacturing, suppliers, logistics, and demand planning
  • Drive the transition from MDD to MDR production across all manufacturing sites
  • Ensure continuous product supply to Asia, MEA, and LATAM regions during re-registration through an effective bridging stock strategy
  • Actively manage inventory build-up and reduction, minimizing obsolete MDD stock and financial impact
  • Coordinate cross-functional activities, aligning on priorities, milestones, risks, and dependencies
  • Serve as the central interface for regional and global stakeholders (Regulatory, Technical Documentation, Supply Chain)
  • Deliver transparent reporting and governance, including SLT updates, risk escalation, and decision support
  • Maintain a stable and scalable global supply chain setup throughout the transition

Required Skills & Experience

  • Proven Project / Program Management experience with ownership of complex, cross-functional workstreams
  • Strong understanding of global manufacturing, supply chain, and logistics operations
  • Experience leading production or operational transitions (e.g., regulatory changes, site transfers, product changes)

Demonstrated ability to:

  • Coordinate multi-functional and international stakeholders

  • Structure complex topics and drive them through execution

  • Proactively manage risks and deliver to tight timelines

  • Experience working across Supply Chain, Production, IT, and Regulatory functions

  • Strong stakeholder management and communication skills, including senior leadership interaction

  • Experience managing inventory strategies (e.g., bridging stock, lifecycle transitions) is highly desirable

  • Familiarity with medical device regulations (MDR/MDD) is a strong advantage

  • Fluent in English and German

FAQs

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