CMF Standard Portfolio Lead – Medical Devices

Materialise; Paris; Sur place; EUR 90 000 - 130 000; Plein temps

Résumé du poste

Materialise Medical seeks a Senior Technical Portfolio Manager for CMF Standard to drive development and commercialization of standard devices. You will lead cross-functional efforts across R&D, manufacturing, quality, and regulatory to remove bottlenecks and accelerate time to market.

You will translate market insights into strategic roadmaps, optimize logistics for customer loan programs in Europe, and ensure alignment with ISO 13485, EU MDR, and global standards while scaling processes across

Qualifications

• Minimum 10 years in CMF standard devices or regulated medical devices.
• Strong knowledge of product R&D, manufacturing, quality, regulatory and supply chain processes.
• Proven ability to scale operational processes across Europe and other regions.

Responsabilités

• Accelerate product development by resolving bottlenecks across R&D, manufacturing, quality, and regulatory.
• Leverage competitor insights to inform launch strategies and improve internal processes.
• Improve customer loan logistics in Europe and beyond with scalable, efficient workflows.
• Define strategic direction and implement a roadmap for the CMF standard portfolio.
• Lead cross-functional change programs while ensuring regulatory compliance and quality.
• Engage stakeholders, communicate progress, and report KPIs and impact.

Connaissances

CMF standard devices

Regulated medical devices

Strategic mindset

Cross-functional leadership

Problem solving

Description du poste

Materialise Medical seeks a Senior Technical Portfolio Manager for CMF Standard to drive development and commercialization of standard devices. You will lead cross-functional efforts across R&D, manufacturing, quality, and regulatory to remove bottlenecks and accelerate time to market.

You will translate market insights into strategic roadmaps, optimize logistics for customer loan programs in Europe, and ensure alignment with ISO 13485, EU MDR, and global standards while scaling processes across