Forward Deployment Lead, R&D Quality Strategy & Transformation

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life‑changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. Purpose The purpose of the Forward Development Lead role is to own end‑to‑end delivery of applications that support the R&D Quality portfolio, from problem identification through production deployment, adoption, and sustained value realization, and to build a team of Forward Deployed Engineers (FDEs) who do the same. FDEs are hybrid technical practitioners embedded with the business, working at the intersection of software engineering, computer system validation, and customer‑facing problem solving. In a GxP‑regulated environment, this role uses Computer System Validation (CSV) procedures as a source of speed and business value, shaping scope, risk categorization, and validation strategy so that compliance accelerates outcomes rather than delaying them. The role collaborates with members of the R&D Quality team, View email address on click.appcast.io delivery partners, Business Quality Assurance (BQA), Computer Systems Quality Assurance (CSQA), and functional leaders across Research & Development at Lilly. The role is accountable for demonstrating value realization across an assigned asset portfolio while developing the next generation of FDEs within Lilly. Responsibilities Own the full lifecycle of an assigned portfolio of quality data and computer system assets, from concept and requirements through deployment, adoption, and sustained business outcomes; no handoffs that diffuse accountability. Author product and system requirements, oversee translation of business problems into technical specifications, and define measurable success criteria against which delivery is evaluated. Operate as a hands‑on technical practitioner: review code, evaluate architecture decisions, quality‑check technical work, and direct internal and external delivery resources. Apply the CSV framework as a delivery accelerator, using GSOP‑1201 and related artifacts to shape validation strategy in service of business outcomes. Build and coach a team of Forward Deployed Engineers, growing the pipeline of technical talent capable of operating at the intersection of business, technology, and quality. Track and report value realization against defined metrics; accountable to the Results Management Office for outcome delivery. Partner with View email address on click.appcast.io, BQA, and CSQA to ensure enterprise alignment, validation compliance, and long‑term sustainability of assets. Own user enablement, adoption strategy, and change management coordination in partnership with OCM resources; success is measured by adoption and business outcomes, not deployment completion. Escalate and manage complex issues, ensuring they are well researched, understood, and resolved. Represent the R&D Quality FDE function in cross‑functional forums, influencing technology and quality decisions across the organization. Basic Qualifications Bachelor’s degree or above in computer science, data analysis, analytics, informatics, life sciences, engineering, or related field. Minimum 5 years of experience in data sciences, product development, computer system delivery, or quality within the pharmaceutical or biotechnology industry, including at least 2 years in a leadership or senior technical capacity. Additional Preferences Advanced degree preferred. Demonstrated experience owning products or capabilities end‑to‑end, from concept through adoption and value realization. Hands‑on technical fluency: ability to write and review code, understand data architectures, and evaluate technical trade‑offs. Working knowledge of CSA, CSV, GxP requirements, and GAMP5; ability to use procedural frameworks to shape delivery strategy rather than treat them as gates. Working knowledge of AI/ML governance in regulated decision‑making, including validation, drift, and lifecycle expectations. Track record of delivering LLM‑based solutions in Clinical, R&D, or regulated Quality settings with measurable business impact (e.g., cycle time, cost, quality, adoption). Experience coaching or developing junior technical staff. Proficiency in scripting languages such as Python for data manipulation and automation. Familiarity with Microsoft Power Platform (Power Apps, Power BI, Power Automate) and enterprise data platforms. Experience with change management and user adoption strategies. Agile or product management experience. Strong ability to communicate technical concepts to both technical and non‑technical stakeholders, including senior leadership. Prior experience in pharmaceutical R&D quality is a strong asset. Additional Information 10% travel may be required. This is an onsite position based in Indianapolis, IN. This is not a remote role. Compensation and Benefits The anticipated wage for this position is $126,000 - $204,600. Full‑time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). Lilly offers a comprehensive benefit program to eligible employees, including: Company‑sponsored 401(k) and pension plans Medical, dental, vision and prescription drug benefits Flexible benefits such as healthcare and/or dependent daycare flexible spending accounts Life insurance and death benefits Paid time off and leave of absence benefits Well‑being benefits (e.g., employee assistance program, fitness benefits, employee clubs, and activities) Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. #J-18808-Ljbffr 100 Eli Lilly and Company