Global Medical Device Program Manager

Hollybank Trustees Ltd; Sunderland; Hybrid; GBP 90,000 - 130,000; Full time

Job summary

Curaleaf International is seeking a senior leader to own and global medical device programmes, overseeing registrations, cross-functional delivery and compliance with EU MDR across multiple territories. You will partner with Product, Regulatory, Commercial and external partners to bring innovative devices to patients worldwide.

You will coordinate with Authorized Representatives, maintain technical files, and drive scalable processes for future market expansion in a fast-paced international

Qualifications

• Direct medical device experience
• Knowledge of EU MDR requirements
• Experience compiling and maintaining technical files and registration dossiers
• Experience managing product registration and market entry across multiple territories
• Ability to work with technical, commercial and regulatory stakeholders
• Strong organisational skills and familiarity with project management tools
• Fluent English; additional European languages are beneficial

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 evidence packs
• Ensure compliance with EU MDR and 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 to senior stakeholders

Skills

Medical device regulation

EU MDR knowledge

Technical documentation

Registration across territories

Cross-functional collaboration

Project management

Fluent English

Tools

PM tools

Job description

Curaleaf International is seeking a senior leader to own and global medical device programmes, overseeing registrations, cross-functional delivery and compliance with EU MDR across multiple territories. You will partner with Product, Regulatory, Commercial and external partners to bring innovative devices to patients worldwide.

You will coordinate with Authorized Representatives, maintain technical files, and drive scalable processes for future market expansion in a fast-paced international