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 within CMF standard 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 do
* Accelerate 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 fast product launch strategies and embed best practices into internal processes
* Improve customer loan logistics in Europe and beyond by implementing efficient, scalable, and customer-friendly processes inspired by industry benchmarks
Define strategic direction and implementation roadmap
* Define a strategic direction for developing and providing the right offering to the market with the market management of the CMF standard portfolio
* Create an ambitious implementation roadmap
* Convince the right stakeholders and drive strategy execution within the organization through effective communication
Product development acceleration
* Map, 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-market
* Identify bottlenecks throughout innovation, design & development (prototyping, testing & verification, validation), industrialization, and regulatory approval stages
* Collaborate with R&D, manufacturing, regulatory, and quality teams to implement optimized processes, especially regarding justification strategies towards notified bodies and national health agencies
Competitor insights and benchmarking
* Conduct deep competitor analysis on the top CMF standard device players
* Translate competitor strategies into actionable improvements in product lifecycle management, operational efficiency, and launch timelines
Change leadership
* Lead cross-functional change program for the CMF standard portfolio with the whole CMF business line, driving and supporting speed-to-market improvement initiatives
* Ensure alignment of acceleration initiatives with regulatory compliance and quality standards
Logistics
* Advise 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 markets
* Integrate best-in-class logistics practices from industry leaders to enhance responsiveness and service quality globally
Stakeholder engagement
* Serve as the high-level central point of contact for all internal product and process projects, including acceleration initiatives across departments and for market requests
* Facilitate communication and coordination between operations, commercial teams, and leadership
* Report regularly on progress, KPIs, and impact
Your profile
* At least 10 years in CMF standard devices (implants and surgical instruments) or regulated medical devices, preferably with senior-level experience at leading companies
* Strong problem-solving skills and advanced knowledge in product R&D, manufacturing, quality, regulatory, and supply chain processes
* Expertise in product development and/or logistics operations (loan, consignment, distributor sales, sterile product handling), plus operational acceleration practices
* Proven track record in reducing time from concept to launch within medical devices
* Understanding of ISO 13485, EU MDR, FDA, and other relevant global regulations and standards
* Proven capability to scale operational processes across Europe and other international regions
* Strategic mindset, strong influencing abilities, collaborative style, and exceptional problem-solving aptitude
Location and type of contract
* Leuven, Belgium
* Full-time
* Hybrid
* Mid-senior level
* CV in English