Experteer Overview
As Technical Portfolio Manager for CMF Standard, you will accelerate development and commercialization of CMF standard devices by removing bottlenecks and streamlining cross-functional workflows.

You’ll drive strategic direction, roadmaps, and process improvements with Ru0026amp;D, manufacturing, quality, and regulatory teams across locations.

Your work spans competitor benchmarking, logistics optimization, and change leadership to shorten lead times and reduce costs.

This role sits at the intersection of product, operations, and regulatory excellence, shaping faster, compliant market access.

You will influence stakeholders globally and champion a culture of continuous improvement.

Compensaciones / Beneficios
• Speed up product development by removing bottlenecks across Ru0026D, manufacturing, quality, and regulatory in multiple locations
• Incorporate competitor insights to inform launch strategies and bake best practices into internal processes
• Define strategic direction and create an ambitious implementation roadmap for the CMF standard portfolio
• Map and improve product and process development workflows from concept to launch to shorten time-to-market
• Collaborate with cross-functional teams to optimize justification strategies for notified bodies and health agencies




• Lead a cross-functional change program to accelerate speed-to-market and ensure regulatory and quality alignment
• Advise on scalable customer loan and consignment processes across markets to improve availability and satisfaction
• Act as the central contact for internal product and process projects and report progress and impact

Responsabilidades
• Minimum 10 years in CMF standard devices or regulated medical devices, with senior-level experience preferred
• Strong problem-solving skills and knowledge of product Ru0026D, manufacturing, quality, regulatory, and supply chain
• Proven experience in product development and/or logistics operations (loan, consignment, distributor sales, sterile handling)
• Track record of reducing time from concept to launch in medical devices
• Understanding of ISO 13485, EU MDR, FDA, and global regulatory standards
• Ability to scale operational processes across Europe and other regions
• Strategic mindset with influencing, collaboration, and strong problem-solving aptitude

Requisitos principales
• autonomy and trust in tasks
• flexible work arrangements
• people-centered culture
• general collaboration
• growth opportunities

📌 Technical Portfolio Manager - CMF Standard (España)
🏢 Materialise
📍 España