Technical Portfolio Manager — CMF Standard

Materialise; Heverlee; Sur place; EUR 110 000 - 140 000; Plein temps

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

At Materialise Medical, we believe that better healthcare starts with solutions designed around the individual patient. If you’re passionate about bringing personalized care to every patient, you’ll love being a part of this team. Through the technology we develop, researchers, engineers, and clinicians are revolutionizing personalized treatment — helping improve and save lives daily.The Technical Portfolio Manager for CMF Standard plays a strategic role in accelerating the development and commercialization of CMF standard devices by removing barriers and streamlining processes. This position oversees the creation of new products and enhancements within the CMF portfolio, ensuring that robust production processes are developed and optimized. Collaborating across cross-functional teams, the role drives process improvements that deliver shorter lead times and reduced cost of goods sold (COGS), helping our products reach the market faster and more efficiently.The ideal candidate brings proven expertise in standard CMF devices or a comparable highly regulated medical device sector, along with strong competitive market knowledge to inform strategic decisions. They are adept at leading organizational change, fostering collaboration, and embedding a culture of continuous improvement across multiple disciplines.What you will doAccelerate product development by resolving bottlenecks and streamlining workflows across R&D, manufacturing, quality, and regulatory in different locations (HQ, France, and Brazil)Leverage competitor insights to understand rapid product launch strategies and embed best practices into internal processesImprove customer loan logistics in Europe and beyond by implementing efficient, scalable, and customer-friendly processes inspired by industry benchmarksDefine strategic direction and implementation roadmapDefine a strategic direction for developing and providing the right offering alongside the market management team for the CMF standard portfolioCreate an ambitious implementation roadmapConvince the right stakeholders and drive strategy execution within the organization through effective communicationProduct development accelerationMap, analyze, and advise on product and process development workflows with R&D and operational teams from concept to launch, with the goal of reducing time-to-marketIdentify bottlenecks throughout innovation, design and development (prototyping, testing, and verification, validation), industrialization, and regulatory approval stagesCollaborate with R&D, manufacturing, regulatory, and quality teams to implement optimized processes, especially regarding justification strategies towards notified bodies and national health agenciesCompetitor insights and benchmarkingConduct deep competitor analysis on the top CMF standard device playersTranslate competitor strategies into actionable improvements in product lifecycle management, operational efficiency, and launch timelinesChange leadershipLead a cross-functional change program for the CMF standard portfolio with the whole CMF business line, driving and supporting speed-to-market improvement initiativesEnsure alignment of acceleration initiatives with regulatory compliance and quality standardsLogisticsAdvise on the design and implementation of efficient and scalable customer loan and consignment setups in multiple markets, enabling cost-effective product availability with high satisfaction levels in multiple marketsIntegrate best-in-class logistics practices from industry leaders to enhance responsiveness and service quality globallyStakeholder engagementServe as the high-level central point of contact for all internal product and process projects, including acceleration initiatives across departments and for market requestsFacilitate communication and coordination between operations, commercial teams, and leadershipReport regularly on progress, KPIs, and impactYour profileMinimum 10 years in CMF standard devices (implants and surgical instruments) or regulated medical devices, preferably with senior-level experience at leading companiesStrong problem-solving skills and advanced knowledge in product R&D, manufacturing, quality, regulatory, and supply chain processesExpertise in product development and/or logistics operations (loan, consignment, distributor sales, sterile product handling), plus operational acceleration practicesProven track record in reducing time from concept to launch within medical devicesUnderstanding of ISO 13485, EU MDR, FDA, and other relevant global regulations and standardsProven capability to scale operational processes across Europe and other international regionsStrategic mindset, strong influencing abilities, collaborative style, and exceptional problem-solving aptitudeWhat’s waiting for youWork that mattersThe technology we build at Materialise pushes the boundaries. You’ll find pride in building something that matters, whether you designed it, printed it, or shipped it. No matter your role, we unlock new possibilities to build a better and healthier world every day.At Materialise, we expect you to think about the customer, not just the task. You push for better solutions and care about the difference your work makes.A people-centered spaceWhen you join Materialise, you join a group of colleagues invested in you, not just your work. From your own team to a department across the world, you’ll find a sense of belonging with people who help without being asked, challenge you, and have your back.At the same time, we expect you to invest in the people around you — not just your own work — to make the group stronger than the sum of its parts.An environment of trustAs a company of innovators, we know how crucial autonomy is in your work. When we hire you, we trust in your expertise, giving you space to organize your tasks, work flexibly, and make your own calls.At Materialise, we expect you to deliver on that trust and keep your commitments.A career ready to buildWhen you see opportunities for your career to grow at Materialise, we encourage you to go for them. People shape a fulfilling career at their own pace here.At Materialise, we expect you to take initiative in your own development. Don’t wait for someone else to plan your career. Step into the space and make it count.Make a difference together with the Medical team.