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Lilly’s BioTDR division in San Diego is expanding its computational capabilities to build a generative design platform for antibodies and biotherapeutics. You will join a cross-functional team applying AI/ML, protein engineering, automation, and structural biology to enhance design, evaluation, and learning cycles.
The role emphasizes rigorous data analysis, model evaluation, and collaboration with wet-lab scientists to translate results into improved designs and performance.
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.
At Lilly, we unite caring with discovery to make life better for people around the world. For more than 25 years, Lilly's Biotechnology Discovery Research (BioTDR) organization has advanced novel antibody and peptide therapeutics from concept through clinical development to market in areas of high unmet medical need.
This role is based at the Lilly Biotechnology Center in San Diego, where we are expanding our computational capabilities to build a generative design platform. By bringing together AI/ML, protein engineering, automation, structural biology, and high-throughput experimentation, BioTDR is creating an integrated de novo design platform capable of generating, ranking, and optimizing novel therapeutic antibodies and other biotherapeutics with improved activity, safety, manufacturability, and target coverage. Designs are rapidly evaluated through experimental validation, creating a continuous learning cycle that strengthens both models and discovery outcomes. The program is supported by dedicated capacity on LillyPod, our wholly owned 1,016-GPU NVIDIA Blackwell Ultra SuperPOD.
Help us push the de novo protein design frontier beyond binders to molecules that can become medicines, faster. Ready to make an impact? Join us.
You will perform rigorous evaluation and validation analyses that translate experimental evidence into actionable insights for improving Lilly's de novo design capabilities. You will curate datasets, compare computational predictions with experimental outcomes, conduct biophysical and physics-based analyses, and work across multidisciplinary teams to identify model and design limitations and inform subsequent design cycles. This is a hands-on scientific role with opportunities to own technical problems and contribute directly to the continuous learning loop that improves de novo design quality and efficiency.
Evaluation analysis. Assemble held-out datasets, compare computational predictions with experimental outcomes, quantify uncertainty, and identify patterns, limitations, and failure modes that inform subsequent model and design improvements.
Biophysical calculations. Run molecular simulation, energy-based, and structure-based analyses and evaluate features for stability, aggregation, and developability prediction, determining where these approaches add value alongside ML-based methods.
Data pipelines. Build reproducible workflows that preserve design, sample, assay, and experimental metadata.
Experimental partnership. Work with protein science and automation colleagues to plan informative data-generation studies and ensure resulting data are suitable for model evaluation, refinement, and subsequent learning cycles.
Closed-loop learning. Integrate positive, negative, and ambiguous experimental outcomes into evaluation datasets and training-ready data products, and help translate those findings into recommendations for subsequent model and design iterations.
Scientific communication. Present findings, uncertainty, model limitations, and experimental evidence clearly to computational and experimental teams, translating results into actionable recommendations for subsequent work.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
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.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include:
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $168,000 - $268,400
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).
In addition, Lilly offers a comprehensive benefit program to eligible employees, including:
Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.