We are growing. And we are looking for talented people. At Decskill, we believe that technological excellence is driven by human talent. We are an IT consulting company with more than 10 years of consolidated experience in the market, focused on building long-term relationships with both our clients and our people. Today, we are a community of over 800 professionals, working from Lisbon, Porto, and Madrid, contributing to impactful technology initiatives. As part of the Astek Group, we combine a strong local culture with a global presence, being active in around 23 countries across 4 continents. This allows us to offer an international context, diverse challenges, and long-term career opportunities, while staying close to our teams. Are you looking for an environment that values curiosity and commitment? Here, your contribution has real impact and individual growth is taken seriously. Mandatory Requirements Experience in Clinical Trial labelling activities. Experience creating and managing Clinical Trial Master Labels. Knowledge of Clinical Supply Chain, Clinical Packaging and Labelling processes. Strong attention to detail and ability to perform quality-critical reviews. Experience working in a regulated pharmaceutical environment (GMP/GxP). Ability to review multilingual label content and ensure regulatory compliance. Experience preparing documentation for regulatory submissions. Fluent English (written and spoken). Ability to work effectively within global and cross-functional teams. Strong organisational skills and ability to manage multiple priorities and deadlines. Preferred Requirements Degree in Life Sciences, Pharmacy, Biotechnology, Chemistry or a related field. Minimum 2 years of experience in the pharmaceutical industry. Experience in Clinical Good Manufacturing Practice (cGMP) environments. Experience in Quality, Compliance or Regulatory Affairs functions. Experience working with external vendors (translation providers, packaging suppliers, etc.). Auditing experience. Experience assessing quality and compliance-related activities. Technical Skills Experience with Clinical Label Management systems. Knowledge of SMARTLS Compliance Author. Knowledge of Adobe InDesign. Knowledge of Prisym 360. Understanding of Clinical Trial packaging, labelling and distribution processes. Knowledge of Clinical Supply Chain requirements and GMP regulations. What you can expect from us Long-term projects with national and international context Opportunities to grow technically and professionally A people-first culture, focused on transparency and trust Teams that value ownership, collaboration and stability At Decskill, we are committed to equal opportunities and non-discrimination. We promote a culture of diversity and inclusion, where recruitment and career progression are based solely on talent, regardless of age, gender, ethnicity, race, nationality, or any other form of discrimination incompatible with human dignity. #J-*****-Ljbffr