Senior Specialist, Technical Product Analyst

Role: Senior Specialist, IT within the RDLM Product Team supporting Digital Regulatory & Safety in Clinical Development. Focuses on delivering and optimizing regulatory lifecycle and document management capabilities, emphasizing business process analysis, requirements management, and solution configuration in a regulated environment. Responsibilities include collaborating with stakeholders, translating business needs into technical requirements, supporting product roadmap execution, analyzing processes for improvement, and managing requirements via JIRA. Qualifications: Bachelor's in IT, Business, or related field; 5+ years in product or business analysis, preferably in life sciences or healthcare; experience with SDLC and delivery methodologies including Agile. Preferred: hands-on Veeva RIM experience, familiarity with regulatory operations, GxP/GMP, and project management certifications. High-Value: Emphasis on regulatory lifecycle management, document management, GxP compliance, in a highly regulated, possibly GxP/GMP environment. Work setup: Hybrid model; no travel specified.