Global Medical Device Program Lead

Curaleaf International; United States; Hybrid; GBP 90,000 - 120,000; Full time

Job summary

Curaleaf International is seeking a Senior Manager to own the global medical device programme, leading day-to-day operations, registrations and cross-functional delivery across international markets.

You will coordinate regulatory compliance (EU MDR and non-EU frameworks), maintain technical files, and report to the Director of Product & Projects, enabling expansion while collaborating with regulatory, commercial and technical teams.

Qualifications

• Hands-on ownership of a medical device project.
• Working knowledge of EU MDR requirements.
• Experience compiling technical documentation and registration dossiers.
• Experience managing product registrations across multiple territories.
• Ability to work with technical, commercial and regulatory stakeholders.
• Strong organisational skills and experience with project management tools.
• Fluent English; additional European languages helpful.
• Experience with non-EU device frameworks would be advantageous.

Responsibilities

• Own day-to-day management of the medical device programme.
• Lead international product registration and market entry activities.
• Coordinate cross-functional projects across multiple territories.
• Maintain technical files, registration dossiers and evidence packs.
• Ensure compliance with EU MDR and market-specific requirements.
• Coordinate with Authorized Representatives and in-market partners.
• Support post-market surveillance and incident trend tracking.
• Develop scalable processes to support future market expansion.
• Provide global programme reporting to senior stakeholders.

Skills

Medical device experience

EU MDR

Dossier maintenance

Market entry

Regulatory coordination

PM tools

Fluent English

Stakeholder management

Job description

Curaleaf International is seeking a Senior Manager to own the global medical device programme, leading day-to-day operations, registrations and cross-functional delivery across international markets.

You will coordinate regulatory compliance (EU MDR and non-EU frameworks), maintain technical files, and report to the Director of Product & Projects, enabling expansion while collaborating with regulatory, commercial and technical teams.