SpliceBio is a biotechnology company developing the next generation of genetic medicines through its proprietary Protein Splicing platform. Our mission is to unlock the potential of gene therapy by enabling the delivery of therapies beyond the size limitations of conventional approaches, with the goal of addressing diseases with significant unmet medical need.Built on more than 20 years of pioneering research in inteins and protein engineering from the Muir Lab at Princeton University, SpliceBio is headquartered in Barcelona and operates in a highly collaborative, international environment.The RoleAs Regulatory Affairs Manager, you will play a key role in shaping and executing regulatory strategies across our development programs. Working closely with the VP of Regulatory Affairs &

• Quality Assurance and cross-functional teams, you will drive integral regulatory activities, support interactions with health authorities, and help advance innovative gene therapies for patients with high unmet medical needs.This role supports the company's gene therapy development programs and contributes to interactions with the FDA, EMA and other Regulatory Authorities.Regulatory Strategy &

• SubmissionsEnsure that the content, quality and format of regulatory submissions comply with applicable regulations and guidelines.Drive the preparation of regulatory applications, including Orphan Drug Designation applications, INDs/CTAs, Scientific Advice procedures, Paediatric Investigation Plans (PIPs), and NDAs/MAAs.Support the development and execution of regulatory strategies that facilitate successful product development and registration.Regulatory Authority InteractionsManage and coordinate interactions with internal and external stakeholders, including the EMA, FDA and other Regulatory Authorities, on behalf of the company.Development Strategy InputContribute to the design and execution of development strategies,



with a particular focus on regulatory considerations, for assigned products.Systems &

• Process ManagementDevelop and maintain Regulatory Affairs systems, processes and procedures to support regulatory submissions, approvals and regulatory intelligence activities.Regulatory IntelligenceMonitor the evolving regulatory landscape, particularly within gene therapy, rare diseases and ophthalmology.Cross-Functional CollaborationPromote effective collaboration across Regulatory Affairs and multidisciplinary development teams, including CMC, Clinical and Preclinical functions.Provide regulatory guidance to support key project decisions and milestones.Global Regulatory CoordinationProject manage and/or support regulatory activities in the EU, US and other international markets in partnership with local consultants and regulatory specialists.What We're Looking ForBSc in a scientific discipline (MSc preferred)5-10 years of Regulatory Affairs experience within the pharmaceutical or biotechnology industryProven experience with EU and US regulatory submissionsStrong understanding of the European and US regulatory landscapeExperience in gene therapy is highly desirable. We also welcome candidates with backgrounds in cell therapy, biologics, or small molecule developmentExperience working in rare diseasesKnowledge of gene therapy regulatory requirements, including GMO regulations, containment requirements, and long-term follow-up protocols, is a strong advantageExposure to ophthalmology programs is a plusExperience with Chinese regulatory authorities and submissions is considered an assetStrategic mindset with the ability to assess and mitigate regulatory risks throughout drug developmentStrong communication and stakeholder management skills, with the ability to collaborate effectively across multidisciplinary teamsFluent English required (written and spoken)

• Spanish is a plusWhy Join SpliceBio?

📌 Compliance Manager (Barcelona)
🏢 SpliceBio
📍 Barcelona