We are looking for a motivated and detail‑oriented QA Officer to join our Quality team. In this role you will support the maintenance of our Quality Management System, ensure compliance with regulatory standards, and contribute to continuous improvement across operations. You will work closely with internal teams, suppliers, and stakeholders to uphold our high quality standards.

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.

Our Values:Lead & Inspire, Commit to Win, Driven to Deliver Excellence, Customer Obsession,One Curaleaf

✅ Key Responsibilities

- Follow, promote and enforce SOPs, work instructions, company policies and procedures

- Support a culture of continuous quality improvement throughout the business

- Assist with the Quality Management System: timely complaint handling, deviation management, recalls, CAPA implementation, and audit support

- Support investigations into supplier non‑conformances; ensure root‑cause analysis and corrective actions are effective

- Contribute to new projects, review supplier qualification requirements, and keep related records up to date

- Maintain quality technical agreements and ensure full compliance with cGMP regulations

• - Assist with training for Quality and Production teams