Lilly Posted October 27, 2026

Advisor, Design Validation & Learning, Biotherapeutics

San Diego, California, United States of America FULL_TIME
Quality Associate
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About this opportunity

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.

Primary Responsibilities

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.

Basic Requirements

Ph.D. in computational biology, biophysics, computational chemistry, bioengineering, chemical engineering, physics, statistics, or a related STEM discipline; or an M.S. with 3+ years; or a B.S. with 5+ years.

Proficiency in Python and the scientific computing stack, version control, and reproducible analysis.

Working knowledge of statistics, uncertainty quantification, regression, agreement metrics, calibration, and experimental design.

Additional Preferences

Hands-on use of OpenMM, GROMACS, Amber, Rosetta, Schrödinger, or related simulation tools.

Understanding of protein structure and biophysics and of binding, expression, and stability measurements.

Experience with protein language models, structure prediction, docking, or molecular scoring.

Experience working with binding and biophysical measurements such as SPR, BLI, thermostability, expression, deep mutational scanning, or other high-throughput biological datasets.

Experience with antibody or VHH developability.

Experience with workflow tools such as Snakemake, Nextflow, containers, or scheduled cluster/GPU computing.

Direct wet-lab experience or close collaboration with experimental scientists.

Strong written and verbal communication skills, including the ability to communicate quantitative findings, uncertainty, and model limitations to computational and experimental scientists.

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: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

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 eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).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.

#WeAreLilly

Job details

Seniority
Associate
Function
Quality
Therapeutic area
Not listed
Location
San Diego, California, United States of America
Employment type
FULL_TIME

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 377 comparable Associate Quality roles across 79 biopharma companies.

377Comparable roles tracked
337Currently active
79Companies hiring similar roles
30Countries represented

Salary context

53 of 377 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $168,000/yr – $268,400/yr
Lowest disclosed · Associate I, Quality Control, Raw Materials · ModernaTX, Inc. $53,500/yr – $85,600/yr
Peer group range $69,550 – $186,375 (median $159,000)

Where these roles are based

Top locations among the 377 comparable roles

United States137
Germany42
France42
China25
India21
Ireland19

+ 24 more countries

Seniority mix

377 of 377 peers have a known seniority level

Manager202
Intern/Fellow/Postdoc99
Associate76

Therapeutic area mix

0 of 377 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Merck KGaA · Milwaukee, Wisconsin, United States · Associate
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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.