Director, Regulatory Technology

Role: Lead the strategic technology and systems development for Regulatory Affairs, Regulatory Operations, and Medical Writing within a biopharma context focused on RNAi therapeutics. Responsibilities: define and execute the technology roadmap, oversee digital workflows, and enhance platforms supporting regulatory information management, submission planning, document authoring, and content reuse. Lead cross-functional collaboration with internal teams and external vendors, ensuring compliance, inspection readiness, data security, and process efficiency across global regions. Provide architecture leadership for regulatory data, content, and platform integrations, enabling analytics, lifecycle management, and innovation in digital capabilities. Qualifications: degree in IT, Computer Science, or related field; proven experience in regulated life sciences, especially in GxP environments; expertise in regulatory systems such as Veeva, RIM, or similar platforms; strong strategic, technical, and problem-solving skills; leadership experience preferred. High-Value: focus on regulatory data architecture, content management, system validation, and cross-system integration; support for global regulatory submissions and inspection readiness. WorkSetup: role entails strategic partner and leadership responsibilities, with a focus on technology roadmap and platform governance.