QUALITY ASSURANCE OFFICER

Curaleaf Inc, a publicly listed business and the world’s largest cannabis company, generating annual revenues of in excess of USD 1.2bn and with a market cap of USD 6 bn. At Curaleaf, we have spent the last decade driving the cannabis health movement and providing people across America with quality product they can rely on. Now we’ve gone International, joining forces with European leaders in the development and production of medical cannabis and a unique, vertically integrated model. Curaleaf International is the International operating arm of Curaleaf Inc. The company is currently selling within the Medical market in the UK, Germany, Italy, Switzerland, the Nordics, Poland and Israel. In addition, it is working towards launching directly into the Adult Use market that is in the process of legalising in Germany. Markets covered: UK, Germany, Switzerland, Italy, Nordics and Poland (medical markets) Our Vision: To enhance lives by cultivating, sharing and celebrating the power of the plant. 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 Overview: We are seeking a highly motivated and detail-oriented Quality Assurance Specialist to join our team. The successful candidate will be responsible for ensuring that our products, processes, and procedures comply with applicable quality standards and regulations. This role is pivotal in maintaining our commitment to delivering high-quality products to our customers. Be based in our facility in Setubal (Parque Industrial Bluebizz). Main Responsibilities: Ensure that the product, processes, and procedures comply with applicable quality standards and regulations. Responsible for the elaboration and revision of Standard Operation Procedures (SOPs), Work Instructions, and other relevant documents. Documentation controller: Ensure documents are stored, traceable, and retrievable through the approved retention policy. Responsible for Batch documentation review in accordance with Good Documentation Practices (GDP), internal approved SOPs, and company policies. Assure training to the team on quality-related topics. Deploy and monitor Deviations, Risk Management reports, Change Controls, Corrective and Preventive Actions (CAPAs), and Investigations, whenever applicable. Execute Product Quality Reviews. Manage all complaints received, ensuring timely and effective resolution. Act as the point of contact with clients and/or suppliers for all quality-related matters. Manage the qualification of clients and suppliers. Provide support during internal and external audits and regulatory inspections. Perform visual quality inspections of the product during the production process. Participate in quality-related projects, as assigned. On a site job - facility in Setubal (Parque Industrial Bluebiz) Degree in Quality, Chemistry, Pharmaceutical Sciences, or a related field. Experience in Good Manufacturing Practices (GMP). Fluent in English, both written and verbal. Strong ability to communicate effectively within different cultural and functional backgrounds. Strong analytical and problem-solving skills. Strong organizational skills. Pro-active and empathetic approach to tasks. Multitasking mindset with the ability to handle multiple projects simultaneously Curaleaf International are committed to a diverse and inclusive workplace. Curaleaf International is an equal opportunity employer and does not discriminate on the basis of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.