Precision. Purpose. Progress.

Step into the fast-growing world of medical cannabis as a Quality Assurance Technician at Curaleaf International — where your eye for detail helps deliver life-changing treatments across the globe.

At Curaleaf International, we're not just participating in the cannabis industry—we're leading it.

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; Four20 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 Vision: To shape the future of cannabis through our commitment to research and product excellence

Our Mission: To be the world’s leading cannabis company consistently delivering superior products and services and driving the global acceptance of cannabis.

Our Values:

• Lead & Inspire
• Commit to Win
• Driven to Deliver Excellence
• Customer Obsession
• One Curaleaf
  
  

Position:

As a Quality Assurance Technician, you will play a crucial part in ensuring the accuracy of our products, contributing directly to our mission of bringing vital medicines to patients. Your duties will include, but not be limited to:

• Record keeping, including controlling and maintaining the document management system.
• Reviewing protocols and material specifications, including raw materials, intermediates, final products, and auxiliary materials.
• Ensuring all current data integrity requirements are met.
• Investigating and concluding critical deviations and any quality-related complaints.
• Documenting approval of critical suppliers of raw materials, intermediates, and packaging materials.
• Reviewing and issuing documents and protocols, including Master Sheets.
  
  

Requirements:

If you are motivated, proactive, and highly organised, this position offers opportunity to participate in shaping the company as it continues to grow. To be successful in this role, it is essential you:

• Have good attention to detail and accuracy.
• Can manage multiple tasks simultaneously and meet deadlines.
• Are adaptable and value learning and development.
• Can communicate clearly and effectively in Spanish and English, particularly in written format.
• Collaborate effectively across departments.
• Hold a pre-university higher degree (Grado Superior) in a scientific discipline, ideally related to pharmacy or chemistry.
  
  

Although not essential, a degree in Chemistry or Pharmacy and relevant experience within the pharmaceutical industry would be highly beneficial.

Other information:

If this sounds like an ideal role for you, don’t delay in getting your application in! This vacancy may be closed early due to a high level of interest.