Global Medical Device Program Lead

Curaleaf International; Greater London; On-site; GBP 90,000 - 125,000; Full time

Job summary

Curaleaf International seeks a seasoned Programme Manager to own its global medical device programme and drive day-to-day management across markets. You will coordinate regulatory, clinical, commercial and technical activities to bring innovative products to patients worldwide.

Reporting to the Director of Product & Projects, you will lead cross-functional projects, ensure EU MDR compliance, maintain technical files, and oversee registrations and new market entries across multiple territories in

Qualifications

• Direct medical device experience with hands-on ownership of a device.
• Strong programme management across multiple markets.
• Working knowledge of EU MDR requirements.
• Experience compiling and maintaining technical documentation, registration dossiers and evidence packs.
• Experience managing product registration and new market entry across multiple territories.
• Confidence working across technical, commercial and regulatory stakeholders.
• Strong organisational skills and experience using project management tools.
• Fluent English; additional European languages beneficial.
• Experience with non-EU device frameworks (e.g., TGA) advantageous.

Responsibilities

• Own the day-to-day management of Curaleaf's medical device programme.
• Lead international product registration and new market entry activities.
• Manage complex cross-functional projects across multiple territories.
• Compile and maintain technical files, registration dossiers and supporting evidence packs.
• Ensure compliance with EU MDR and applicable market-specific requirements.
• Coordinate with Authorised Representatives and in-market partners.
• Support complaint handling, post-market surveillance and incident trend tracking.
• Develop scalable processes and systems to support future market expansion.
• Provide clear global programme reporting and updates to senior stakeholders.

Skills

Medical device PM

EU MDR knowledge

Technical documentation

Cross-functional leadership

Regulatory submissions

English fluency

Job description

Curaleaf International seeks a seasoned Programme Manager to own its global medical device programme and drive day-to-day management across markets. You will coordinate regulatory, clinical, commercial and technical activities to bring innovative products to patients worldwide.

Reporting to the Director of Product & Projects, you will lead cross-functional projects, ensure EU MDR compliance, maintain technical files, and oversee registrations and new market entries across multiple territories in