Medical Device Manager

Flexible across Curaleaf International site locations. Some national and international travel required.

Director of Product & Projects

Curaleaf International is shaping the future of cannabis through its commitment to research and product excellence. Powered by a strong presence at all stages of the supply chain, its unique distribution network throughout Europe, Canada and Australasia brings together pioneering research with cutting-edge cultivation, extraction, and production. Amidst a rapid growth trajectory, the emphasis on quality and expertise aims to ensure the delivery of safe and legal cannabis.

Curaleaf International's network includes a clinic, pharmacy, and laboratory in the UK; cultivation and EU-GMP processing facilities in Portugal; an EU-GMP processing, quality assurance and research site in Spain;
Four 20 Pharma wholesaler and distributor in Germany; a Polish wholesaler and clinic; and the EU-GMP producer Northern Green Canada.

Curaleaf International is part of Curaleaf Holdings, Inc., a leading international producer and distributor of consumer cannabis products.

This is a unique opportunity to take ownership of a global medical device programme at an exciting stage of growth.

You'll lead the day-to-day management of the medical device portfolio, oversee new market registrations, coordinate complex cross-functional programmes and ensure compliance with relevant regulatory frameworks. Working closely with Product, Regulatory, Commercial and external partners, you'll play a key role in bringing innovative products to new patients and markets around the world.

• 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.

• Direct medical device experience, with hands-on ownership of a specific device.
• 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, with additional European languages beneficial.
• Experience with TGA or other non-EU device frameworks would be advantageous.

• Highly organised and detail-oriented.
• Comfortable managing multiple work streams and documentation-intensive activity.
• Equally capable of operating strategically and executing hands-on.
• A proactive problem solver who thrives in a fast-paced international environment.
• Collaborative, commercially aware and able to influence stakeholders across markets.

This role offers the opportunity to take ownership of a global medical device programme and help shape future international market expansion. You'll work closely with senior leaders and play a key role in delivering innovative healthcare products across multiple international markets.