CMF Medical Portfolio Lead - Strategy & Acceleration

Materialise

Heverlee

Sur place

EUR 110 000 - 140 000

Plein temps

14 jours+
Générateur de candidature

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Résumé du poste

Materialise is seeking a Technical Portfolio Manager for CMF Standard to accelerate development and commercialization. You will drive cross-functional improvements across R&D, manufacturing, quality and regulatory to shorten lead times and reduce COGS while aligning with market needs.

With 10+ years in CMF or regulated medical devices, you will translate competitive insights into faster product launches and scalable processes across Europe.

Qualifications

  • Minimum 10 years in CMF standard devices or regulated medical devices.
  • Strong knowledge of product development, manufacturing, quality, regulatory, and supply chain processes.
  • Experience with ISO 13485, EU MDR, FDA, and related global standards.
  • Ability to scale operational processes across Europe and other regions.
  • Strategic mindset with collaborative leadership and problem-solving aptitude.

Responsabilités

  • Accelerate product development by removing bottlenecks and speeding time-to-market.
  • Map and optimize workflows across R&D, manufacturing, quality, and regulatory teams.
  • Lead cross-functional change programs for CMF standard portfolio.
  • Derive competitor insights and translate into actionable improvements.
  • Advise on logistics models for loan/consignment across markets.
  • Engage stakeholders and report progress and KPIs to leadership.

Connaissances

CMF devices experience
Regulatory knowledge
Process optimization
R&D/manufacturing/quality/supply chain
Product development
Logistics operations
Cross-border scaling
Strategic influencing
Problem solving

Description du poste

Materialise is seeking a Technical Portfolio Manager for CMF Standard to accelerate development and commercialization. You will drive cross-functional improvements across R&D, manufacturing, quality and regulatory to shorten lead times and reduce COGS while aligning with market needs.

With 10+ years in CMF or regulated medical devices, you will translate competitive insights into faster product launches and scalable processes across Europe.

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