Regeneron
SeniorManager,ProductManager-Delivery&OperationsProductLead–EnablingTechnologies
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“Senior Manager, Product Manager - Delivery & Operations Product Lead – Enabling Technologies at Regeneron. Skills: Generative AI, Product management, GxP implementation. Lead stand-ups. Refine backlogs”
What You'll Achieve.
Accelerate content creation; Improve quality; Reduce cycle times
Industry & Context.
Root cause analysis
What They're Looking For.
Must Have
8-10 years validated experience, 6+ years as an equivalent, 3 years in enterprise SaaS, 1+ year delivering generative/agentic-AI solutions, GxP implementations of AI document-authoring platforms, Agile/DevOps methods, RAG, MCP, LLMs, Copilot, Claude, Integration across Clinical, Regulatory, and Medical Affairs systems
What You'll Do.
Prioritize enhancements
Review solution architecture
Track sprint progress
Update program leadership
Coordinate change-control
Monitor platform adoption
Identify automation opportunities
How You'll Work.
Team & Collaboration
Business and technology stakeholders; Clinical, Regulatory, Medical Affairs teams; Data-science teams
Communication Scope
Executive stakeholders
Process & Methodology
Roadmap, Agile, DevOps
Full Job Description
Global Development IT is seeking a strategic, hands-on Senior Manager to serve as Product Lead for Regeneron’s enterprise generative-AI document-authoring platform. You will be responsible for a multi-phase implementation that delivers governed, scalable AI capabilities across Clinical, Regulatory, Medical Affairs, Labeling, and other Global Development domains. Partnering with business and technology stakeholders, you will align platform strategy to scientific, regulatory, and operational needs, ensuring secure, compliant, and high-impact outcomes. Reporting to the Associate Director, Product Management of Enabling Technologies, you will drive the full product lifecycle—from vision and roadmap through design, build, validation, launch, and optimization. Your blend of clinical-process know-how, agile product leadership, and deep AI expertise will accelerate content creation, improve quality, and reduce cycle times for regulated documents. **In this role, a typical day might include the following:** \- Leading stand-ups, refining backlogs, and approving user stories for AI-powered authoring features \- Facilitating workshops with Clinical, Regulatory, and Medical Affairs teams to gather requirements and prioritize enhancements \- Reviewing solution architecture to enforce security, privacy, and GxP compliance across RAG, MCP, LLM, Copilot, and Claude integrations \- Tracking sprint progress, surfacing risks, and updating program leadership on scope, budget, and ROI \- Defining guardrails for citizen development and coordinating change-control / governance forums \- Monitoring platform adoption and performance to identify automation and continuous-improvement opportunities **This job might be for you if you:** \- Translate sophisticated Global Development document workflows into intuitive, AI-enabled products \- Excel at influencing cross-functional teams without direct authority and communicating clearly with executive stakeholders \- Thrive in agile environments, ba
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