Quality Control Analyst

Job Vacancy:
Quality Control Analyst

Location:

Sunderland, UK

Industry: Pharmaceutical / Regulated Manufacturing

Type:
Full-time on site

We are seeking a detail‑oriented Quality Control Analyst to join our laboratory team, delivering accurate, compliant testing that underpins the safety and quality of our raw materials and finished products. You will perform chromatographic and wet chemistry analysis aligned with pharmacopoeia standards, support method development, and uphold GMP/GDP requirements across all activities. If you thrive in a precise, regulated environment and want to grow your technical expertise, this is the ideal role for you.

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

• Manage laboratory reagents and consumables to ensure uninterrupted testing workflows
• Operate, calibrate, and maintain all lab equipment in strict compliance with GMP, GDP, and Health & Safety standards
• Review raw material documentation from suppliers to confirm suitability for manufacturing use
• Perform comprehensive testing of raw materials and finished products, including HPLC, FTIR, and wet chemistry techniques, to support approval processes
• Conduct analytical method transfers and development activities following approved protocols and under the guidance of the Quality team
• Support stability programmes through timely sample pull‑point management and analysis
• Author laboratory reports and technical documents for method development and transfer
• Oversee raw material purchasing, handling, sampling, and final approval
• Collaborate with Production teams to prioritise and schedule manufacturing in line with quality requirements
• Complete mandatory training and pursue ongoing professional development
• Represent the company professionally with suppliers, clients, and internal stakeholders
• Adhere fully to HR policies, Health & Safety regulations, and strict confidentiality requirements
• Work flexibly to meet business needs while maintaining the highest professional standards

• Practical knowledge of High Performance Liquid Chromatography (HPLC) and core analytical chemistry laboratory techniques
• Strong proficiency in Microsoft Office suite
• Highly organised, with the ability to maintain accurate, contemporaneous records compliant with ALCOA+ principles
• Inquisitive, solution‑focused mindset; skilled at systematic problem‑solving and root‑cause analysis
• Bachelor's degree (or higher) in Life Sciences, Chemistry, or a related discipline is preferred – relevant equivalent experience will also be considered

• Competitive salary
• 27 days annual holiday + 8 bank holidays
• Private medical insurance
• Free on-site parking

• Work within a fast‑growing, purpose‑driven organisation
• Play a key role in shaping how patients access information and support
• Full training provided on regulatory requirements
• Be part of a collaborative team supporting accessible medical care