Qualified Person (QP) & Responsible Person (RP)

The Qualified Person (QP) is responsible for ensuring that each batch of medical cannabis products released for sale complies with applicable laws and regulatory requirements. The QP oversees quality systems, GMP compliance, and batch certification, playing a critical role in maintaining patient safety and product integrity in the pharmacy’s operations. The QP will play a crucial part of the next stage of our growth as we apply for our wholesale and import licenses and act as Responsible Person (RP) across all parts of the business. Role Requirements Key Responsibilities: Batch Certification & Release Certify and release batches of medical cannabis products in accordance with EU GMP and local regulatory standards (e.g., MHRA). Review and approve all documentation relating to the manufacture, testing, and release of products. Supplier qualification and auditing Ensure all suppliers are GMP compliant through thorough qualification and regular auditing Regulatory Compliance Ensure operations are fully compliant with local medical cannabis laws (e.g., Misuse of Drugs Regulations, Controlled Drugs regulations). Serve as the liaison with regulatory authorities during inspections and audits. Quality Assurance Lead and maintain Quality Management Systems (QMS) including CAPAs, deviations, change controls, complaints, and risk assessments. Perform audits of suppliers and contract manufacturers to ensure compliance. Standard Operating Procedures Oversee the creation, approval, and training of SOPs related to production, storage, handling, and dispensing of cannabis products. Pharmacovigilance Monitor and report adverse events related to medical cannabis usage and ensure appropriate follow-up and documentation. Team Collaboration Work closely with pharmacists, cultivation/manufacturing teams, and logistics to ensure quality is maintained across the supply chain. Provide QP oversight and training to junior staff and other departments on quality and compliance topics. Qualifications & Requirements: Legally recognised Qualified Person status under applicable national regulations. Degree in pharmacy, chemistry, biology, or a related scientific discipline. Extensive knowledge of GMP regulations, especially as applied to cannabis-based products for medicinal use. Previous experience working in a GMP-regulated pharmaceutical or medical cannabis environment. Strong understanding of quality systems, regulatory submissions, and pharmaceutical product release. Excellent attention to detail, documentation skills, and regulatory awareness. Ability to manage complex projects and work under pressure to meet deadlines. Preferred Experience: Previous experience in the medical cannabis industry. Familiarity with controlled drug handling and record-keeping. Experience interacting with regulatory agencies (e.g., HPRA, MHRA, EMA). About The Company Montu is the UK’s leading cannabis company with operations globally facilitating access to cannabis through locally integrated ecosystems that streamline the patient experience from end-to-end and set new standards in Cannabis Care. Our mission: improve the lives of millions of people through cannabis therapies. Medical cannabis has already been legalised in more than 50 countries across the world over recent years, unlocking a huge potential for medical and wellness markets. As one of the fastest growing businesses in the industry, Montu is now actively looking to expand the team to take the company to the next level.. We take a technology-first approach to improving the medical cannabis patient experience – whether it’s by delivering best-in-class online clinical care, or through our industry-leading product lines and innovative supply chain management tools. #J-18808-Ljbffr