Senior Program Manager – Europe
We are seeking a strategic and experienced Senior Program Manager to lead the integration of digital solutions into an Class III Medical Device portfolio across the Europe. This role plays a pivotal part in driving digital transformation within the neuromodulation industry by aligning innovation with patient outcomes, regulatory requirements, and business strategy.
About the Role:
As the regional leader for digital integration, you will oversee programs aimed at enhancing medical device offerings with software, mobile applications, and connected technologies. You’ll collaborate across international teams to deliver compliant, user-centered products that elevate care delivery and market competitiveness.
Key Responsibilities:
* Lead the strategy and execution for integrating digital products into medical technology portfolios across European markets.
* Identify innovation opportunities by tracking digital health trends, customer needs, and emerging technologies.
* Oversee full product lifecycle management for digital solutions, from ideation to launch and post-market monitoring.
* Work cross-functionally with technical, clinical, regulatory, and commercial teams to ensure cohesive development and deployment.
* Support international collaboration by aligning EU-specific requirements with global development teams.
* Manage market research, performance analysis, and KPI reporting to inform business decisions and continuous improvement.
* Ensure compliance with European medical device regulations, including MDR, GDPR, and relevant ISO standards.
* Act as a liaison for healthcare professionals and external partners to gather feedback and optimize product performance.
Qualifications:
* Bachelor's degree in Engineering, Life Sciences, or related technical field; an advanced degree (MBA, MSc) is preferred.
* Experience in program or product management within the medical device or digital health industry.
* Demonstrated experience with digital integration into healthcare solutions, ideally involving Class III medical devices.
* Deep knowledge of EU medical regulations and digital health standards.
* Familiarity with software development cycles, user experience design, and connected technologies (IoT).
* Strong organizational, analytical, and project management skills.
* Excellent communication abilities with both technical and non-technical audiences.
* Fluency in English; additional European languages are an advantage.
* Willingness to travel within Europe and occasionally to the US.