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.
What You'll Bring
- 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.
You Are
- 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.
Why Join Us?
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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