Responsibilities Acquire and maintain parallel trading licenses, including dossier preparation, submissions, and lifecycle management Prepare and proofread packaging materials, artwork files, mock-ups, item lists, and regulatory documentation Communicate with competent authorities and stakeholders across assigned markets Participate in continuous improvement initiatives and optimization of processes and systems Support onboarding and training of colleagues within the team Evaluate regulatory legislation changes and contribute to operational implementation Participate in projects as an operational SME within Regulatory Affairs Support maintenance of SOPs, working instructions, and guidelines Requirements 5+ years of experience within Regulatory Affairs A Master’s degree or Ph D within Pharmacy,



Health Sciences, Life Sciences, or similar Alternatively 8+ years of relevant Regulatory Affairs experience Strong understanding of EU regulatory requirements and procedures Professional proficiency in English Professional proficiency in either Spanish and Portuguese / Italian Experience working with packaging materials and documentation in a regulated environment A structured and detail-oriented approach combined with a proactive mindset Experience working with Adobe Creative Cloud in a technical or regulated environment is an advantage #J-18808-Ljbffr

📌 Associate specialist, regulatory affairs (Madrid)
🏢 Jobtailor
📍 Madrid