QA ADMINISTRATOR

Are you measured in your approach to work, able to retain attention to detail in all situations? Do you understand the importance quality plays in ensuring a safe pharmaceutical service? Do you want a job that really makes a difference to others? Join us here at Curaleaf! We are looking to expand our QA team, opening an opportunity for a QA Administrator to strengthen our already fantastic team in the Sunderland office. At Curaleaf International, we're not just participating in the cannabis industry—we're leading it. As part of the world’s largest cannabis company, Curaleaf Holding, Inc., we are powered by a strong presence at all stages of the supply chain. Our unique distribution network throughout Europe, Canada and Australasia brings together pioneering research with cutting-edge cultivation, extraction, and production. Amidst a rapid growth trajectory, our emphasis on quality and expertise aims to deliver safe and legal cannabis. Curaleaf Pharmacy the UK’s first distance selling pharmacy specialising in medical cannabis, is regulated by the GPhC. The pharmacy fulfils medical cannabis prescriptions supporting safe and affordable access to medical cannabis. 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 As a QA Administrator, you will provide support in all quality aspects relating to GMP and GDP functions of the business. You will hold responsibility for the control of all quality related documents, including both initial creation and ongoing revisions, ensuring these are issued and used correctly throughout the company. Duties will include, but not be limited to: Managing the flow of documentation within the organisation, including workflow approvals, sign offs and revision/version control Copying, scanning, and storing documents in an organised manner. Preparing ad-hoc reports on projects as required. Data management in line with up-to-date guidelines. Supporting other departments in following procedures using controlled documentation Regularly auditing company systems to ensure correct and accurate usage We are looking for a motivated problem-solver who is able to work to strict guidelines, while also looking for innovative ways to improve processes in line with our culture of continuous quality improvement. As you will play a crucial part in assuring company quality and compliance, it is important you have previous experience with document management. The essentials: An ability to work in a technical environment, navigating conflicting priorities and constraints Capability to work collaboratively, being an assertive and proactive team member Excellent communication skills Proficient IT skills, including familiarity with Microsoft Office and Sage Strong organisation and prioritisation abilities Flexibility and efficiency in order to meet internal and external needs whilst maintaining the highest possible professional standards Although not compulsory, experience working within a GMP environment would be highly beneficial. We value progression and development, offering lots of opportunity in a rapidly growing organisation. We also offer: Competitive salary Excellent holiday allowance Private medical insurance On-site parking Life insurance 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.