ph3Responsibilities /h3 ul liAcquire and maintain parallel trading licenses, including dossier preparation, submissions, and lifecycle management /li liPrepare and proofread packaging materials, artwork files, mock-ups, item lists, and regulatory documentation /li liCommunicate with competent authorities and stakeholders across assigned markets /li liParticipate in continuous improvement initiatives and optimization of processes and systems /li liSupport onboarding and training of colleagues within the team /li liEvaluate regulatory legislation changes and contribute to operational implementation /li liParticipate in projects as an operational SME within Regulatory Affairs /li liSupport maintenance of SOPs, working instructions,



and guidelines /li /ul h3Requirements /h3 ul li5+ years of experience within Regulatory Affairs /li liA Master’s degree or PhD within Pharmacy, Health Sciences, Life Sciences, or similar /li liAlternatively 8+ years of relevant Regulatory Affairs experience /li liStrong understanding of EU regulatory requirements and procedures /li liProfessional proficiency in English /li liProfessional proficiency in either Spanish and Portuguese / Italian /li liExperience working with packaging materials and documentation in a regulated environment /li liA structured and detail-oriented approach combined with a proactive mindset /li liExperience working with Adobe Creative Cloud in a technical or regulated environment is an advantage /li /ul /p #J-18808-Ljbffr

📌 Associate Specialist, Regulatory Affairs (Madrid)
🏢 Jobtailor
📍 Madrid