Curaleaf International
Operational Quality Supervisor
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About the Role
With a culture of continuous quality improvement, our Quality teams are key to our work here at Curaleaf. As an Operational Quality Supervisor, you will play a vital role in supporting the delivery of high-quality, compliant products by leading the Operational Quality Release team and ensuring effective GMP release processes.
You will be responsible for managing the day-to-day activities of the Operational Quality team, supporting product release, resolving quality issues, and working collaboratively with internal teams to ensure customer and regulatory requirements are consistently met.
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.
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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
In this role, your duties will include, but not be limited to:
- Leading and line managing the Operational Quality Release team to ensure compliance and performance standards are met
- Managing team priorities, projects, and workloads to support effective product release
- Ensuring GMP compliance across product release, pre-manufacture, formulation development and approval, and investigations
- Acting as the Operational Quality subject matter expert during audits and customer and stakeholder queries
- Supporting Quality improvement initiatives, training, and effective use of the Quality Management System
- Collaborating with Quality, Production, and wider teams to resolve issues and support product roll-out
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About You
To be successful within the Quality team, you will be an experienced quality professional with strong leadership skills and a commitment to maintaining the highest standards of GMP compliance. It is essential you:
- Have GMP experience within a pharmaceutical, medical production, or quality environment
- Have experience leading or supervising a quality-focused team
- Have strong knowledge of pharmaceutical quality systems and product release processes
- Thrive in a regulated, fast-paced environment with excellent attention to detail
- Have strong communication, decision-making, and problem-solving skills
- Are proficient in Microsoft Office and confident using quality management systems
Ready to be part of a growing and innovative industry where quality makes a real difference? Apply today and join our team.
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