Global Medical Device Programme Lead

Curaleaf International; England; Hybrid; GBP 70,000 - 110,000; Full time

Job summary

Curaleaf International is seeking a globally focused Regulatory and Product Manager to own the medical device programme across multiple markets. You will drive day‑to‑day management, coordinate registrations and ensure regulatory compliance with EU MDR and market requirements.

Working with Product, Regulatory, Commercial and external partners, you will enable new patient access and support expansion into international markets. Fluent English and strong cross‑functional skills are essential.

Qualifications

• Direct medical device experience with ownership of a device.
• Working knowledge of EU MDR requirements.
• Experience compiling technical files and registration dossiers.
• Experience managing product registrations across multiple territories.
• Experience coordinating with regulatory, commercial and technical stakeholders.
• Fluent English; additional languages advantageous.
• Exposure to non-EU device frameworks is a plus.

Responsibilities

• Own day-to-day management of the medical device programme.
• Lead international product registrations and market entries.
• Coordinate cross-functional projects across territories.
• Prepare and maintain technical files and evidence packs.
• Ensure compliance with EU MDR and market requirements.
• Collaborate with authorised representatives and partners.
• Provide programme updates to senior stakeholders.

Skills

Medical device exp

EU MDR knowledge

Documentation management

Product registrations

Cross-functional collaboration

Project management

Fluent English

Regulatory affairs

Job description

Curaleaf International is seeking a globally focused Regulatory and Product Manager to own the medical device programme across multiple markets. You will drive day‑to‑day management, coordinate registrations and ensure regulatory compliance with EU MDR and market requirements.

Working with Product, Regulatory, Commercial and external partners, you will enable new patient access and support expansion into international markets. Fluent English and strong cross‑functional skills are essential.