Medical Device Manager

Location

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

Reporting to

Director of Product \& Projects

About Us

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.

The Opportunity

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.

What You'll Do

• 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.


• Strong programme management experience 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, 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 workstreams 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.

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