Lilly Posted July 27, 2026

Advisor, Data Scientist - CMC Data Products

Indianapolis, Indiana, United States of America FULL_TIME
Manufacturing & CMC Associate

Lilly is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Organizational & Position Overview:

The Bioproduct Research & Development (BR&D) organization strives to deliver creative medicines to patients by developing and commercializing insulins, monoclonal antibodies, novel therapeutic proteins, peptides, oligonucleotide therapies, and gene therapy systems. This multidisciplinary group works collaboratively with our discovery and manufacturing colleagues.

We are seeking an exceptional Data Scientist with deep data expertise in the pharmaceutical domain to lead the development and delivery of enterprise-scale data products that power AI-driven insights, process optimization, and regulatory compliance. In this role, you'll bridge pharmaceutical sciences with modern data engineering to transform complex CMC, PAT, and analytical data into strategic assets that accelerate drug development and manufacturing excellence.

Responsibilities:

Data Product Development: Define the roadmap and deliver analysis-ready and AI-ready data products that enable AI/ML applications, PAT systems, near-time analytical testing, and process intelligence across CMC workflows.

Data Archetypes & Modern Data Management: Define pharmaceutical-specific data archetypes (process, analytical, quality, CMC submission) and create reusable data models aligned with industry standards (ISA-88, ISA-95, CDISC, eCTD).

Modern Data Management for Regulated Environments: Implement data frameworks that ensure 21 CFR Part 11, ALCOA+, and data integrity compliance, while enabling scientific innovation and self-service access.

AI/ML-ready Data Products: Build training datasets for lab automation, process optimization, and predictive CQA models, and support generative AI applications for knowledge management and regulatory Q&A.

Cross-Functional Leadership: Collaborate with analytical R&D, process development, manufacturing science, quality, and regulatory affairs to standardize data products.

Deliverables include:

Scalable data integration platform that automates compilation of technical-review-ready and submission-ready data packages with demonstrable quality assurance.

Unified CMC data repository supporting current process and analytical method development while enabling future AI/ML applications across R&D and manufacturing

Data flow frameworks that enable self-service access while maintaining GxP compliance and audit readiness

Comprehensive documentation, standards, and training programs that democratize data access and accelerate product development

Basic Requirements:

Master’s degree in Computer Science, Data Science, Machine Learning, AI, or related technical field

8+ years of product management experience focused on data products, data platforms, or scientific data systems and a strong grasp of modern data architecture patterns (data warehouses, data lakes, real-time streaming)

Knowledge of modern data stack technologies (Microsoft Fabric, Databricks, Airflow) and cloud platforms (AWS- S3, RDS, Lambda/Glue, Azure)

Demonstrated experience designing data products that support AI/ML workflows and advanced analytics in scientific domains

Proficiency with SQL, Python, and data visualization tools

Experience with analytical instrumentation and data systems (HPLC/UPLC, spectroscopy, particle characterization, process sensors)

Knowledge of pharmaceutical manufacturing processes, including batch and continuous manufacturing, unit operations, and process control

Expertise in data modeling for time-series, spectroscopic, chromatographic, and hierarchical batch/lot data

Experience with laboratory data management systems (LIMS, ELN, SDMS, CDS) and their integration patterns

Additional Preferences:

Understanding of Design of Experiments (DoE), Quality by Design (QbD), and process validation strategies

Experience implementing data mesh architectures in scientific organizations

Knowledge of MLOps practices and model deployment in validated environments

Familiarity with regulatory submissions (eCTD, CTD) and how analytical data supports marketing applications

Experience with CI/CD pipelines (GitHub Actions, CloudFormation) for scientific applications

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 Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$126,000 - $244,200

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
Manufacturing & CMC
Therapeutic area
Not listed
Location
Indianapolis, Indiana, United States of America
Employment type
FULL_TIME

How this role compares

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

We currently track 240 comparable Associate Manufacturing & CMC roles across 48 biopharma companies.

240Comparable roles tracked
227Currently active
48Companies hiring similar roles
22Countries represented

Salary context

71 of 240 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 $126,000/yr – $244,200/yr
Lowest disclosed · Associate Operator - 2nd Shift · Mylan Technologies, Inc. $30,000/yr – $49,000/yr
Peer group range $39,500 – $186,200 (median $156,390)

Where these roles are based

Top locations among the 240 comparable roles

United States141
India36
Ireland11
Singapore7
China's Mainland6
Netherlands5

+ 16 more countries

Seniority mix

240 of 240 peers have a known seniority level

Manager165
Associate67
Intern/Fellow/Postdoc8

Therapeutic area mix

0 of 240 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
Lilly Boston, Massachusetts, United States of America Associate
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority Same country
60%similar
Merck Rahway, New Jersey, United States of America Associate
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority Same country
60%similar
Sanofi Vaccines US Inc. Waltham, United States Associate
Same function Same seniority Same country

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%
Advisor, Downstream Process Development – Viral Vectors
Lilly · Boston, Massachusetts, United States of America · Associate
Function Therapeutic area Seniority Country
60%
Advisor, Analytical Chemistry
Lilly · Indianapolis, Indiana, United States of America · Associate
Function Therapeutic area Seniority Country
60%
Automation Associate
Regeneron Pharmaceuticals, Inc (USA) · Tarrytown, United States · Associate
Function Therapeutic area Seniority Country
60%
Associate Operator - 2nd Shift
Mylan Technologies, Inc. · St. Albans, United States · Associate
Function Therapeutic area Seniority Country
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.