Senior Specialist, Technical Product Analyst

Role: Senior Specialist, IT within the Regulatory Document Lifecycle Management (RDLM) Product Team, supporting digital capabilities for regulatory operations in a highly regulated environment. Responsibilities: partner with stakeholders to gather and document requirements for regulatory lifecycle and document management, translate business needs into technical solutions, support product roadmap execution, analyze and improve business processes related to Veeva RIM submissions and archives, and manage requirements via JIRA. Qualifications: bachelor’s degree in IT, Business, or related field; 5+ years in product/business analysis within life sciences or healthcare; experience managing complex projects and working with cross-functional teams; strong SDLC, Agile, and regulatory domain knowledge. Preferred: hands-on with Veeva RIM, regulatory lifecycle management, GxP compliance, and expertise with JIRA; certifications in project management or product ownership are a plus. High-Value: focus on regulatory lifecycle management, Veeva RIM, compliance in GxP environments, and supporting digital solutions for regulatory operations. Work setup: hybrid; location unspecified; travel not explicitly required.