Biotech & Pharma TN Sponsorship Jobs in Indiana
Indiana's biotech and pharma sector is anchored by major employers like Eli Lilly in Indianapolis, Cook Medical in Bloomington, and Corteva Agriscience, all of which have a history of sponsoring TN visas for qualified Canadian and Mexican professionals. Roles in research, regulatory affairs, and quality assurance represent the strongest areas of TN-eligible hiring across the state.
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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.
Function: Immunology Informatics / Human Genetics
Level: R5-R6
Location: Indy or Boston
About the Role
The Immunology Informatics team integrates human genetics into drug discovery and development across the autoimmune disease spectrum (rheumatology, gastroenterology, and dermatology). We are seeking a statistical or population geneticist to strengthen our target identification and validation efforts by applying rigorous quantitative genetics methods — including Mendelian randomization, GWAS interpretation, fine mapping co-localization, and multi-omic integration — to identify, prioritize and de-risk therapeutic targets across the immunology pipeline.
This role sits at the interface of human genetics, translational biology, and drug development strategy, working closely with target discovery, translational medicine, statistical, and bioinformatics colleagues, as well as external partners.
Target Evaluation & Genetic Evidence Assessment:
- Lead systematic genetic evidence reviews for existing and emerging immunology drug targets, synthesizing GWAS, exome/whole-genome sequencing, and rare-variant data to assess causal support and directionality (loss-of-function vs. gain-of-function phenotype concordance with therapeutic hypothesis).
- Build and maintain target evaluation frameworks that score genetic evidence quality, effect direction, and development-stage relevance across a target portfolio.
- Interrogate and interpret summary and individual levels data from public and licensed genetic resources (e.g., Open Targets, GWAS Catalog, UK Biobank, AllofUs, FinnGen) to support go/no-go and prioritization decisions for drug targets.
- Propose novel drug targets with strong human causal evidence for autoimmune diseases.
- Make decision enabling judgements on drug target quality strong scientific rationale.
Population Genetics, Mendelian Randomization, Causal Inference:
- Design, execute, and critically evaluate evidence from large population-scale datasets using Mendelian Randomization and other methods to test causal relationships between genetic variants, biomarkers/proteins and immune-mediated disease outcomes.
- Assess genetic instrument validity for Mendelian Randomization, pleiotropy, and sensitivity of MR findings (e.g., MR-Egger, weighted median, colocalization) and communicate limitations clearly to immunologists.
- Collaborate with external genetics partners and academic collaborators on specific genetics programs.
Cross-Functional Collaboration & Communication:
- Translate complex genetic and statistical findings into clear, decision-relevant summaries for target discovery teams, translational scientists, and portfolio governance.
- Contribute genetics-informed input to target nomination packages, competitive intelligence, and program strategy documents.
- Represent statistical genetics perspective in cross-functional target review forums.
Required Qualifications
- Ph.D. in statistical genetics, population genetics, genetic epidemiology, biostatistics, computational biology, or a related quantitative field (or M.D, M.S. with equivalent industry experience).
- Demonstrated experience working on large-scale population datasets, Mendelian randomization (MR) methodology and causal inference from human genetic datasets.
- Strong proficiency in R, ideally within a tidyverse-based workflow; comfort with reproducible, version-controlled analysis (Git); basic knowledge of PLINK or other tools to manipulate large genotype datasets.
Preferred Qualifications
- Practical experience interrogating large-scale genetics/genomics databases (e.g. UK Biobank, AllofUS, Open Targets,) and their APIs.
- Demonstrated proficiency using fine-mapping, and colocalization approaches for GWAS summary statistics to refine association signals and identify causal genetic variants.
- Ability to critically evaluate statistical/analytical pipelines for genetic analysis and communicate methodological trade-offs to interdisciplinary teams.
- Experience in immunology/immune-mediated population genetics.
- Experience integrating multi-omics with genetics data, including pQTL or eqTL analysis.
- Familiarity with drug target identification/validation criteria and workflows in a pharmaceutical or biotech R&D setting.
- Experience collaborating with external genetics/data partners or academic consortia.
What Success Looks Like in This Role
- Providing a defensible, well-documented genetic evidence assessment that underpins target prioritization decisions across the immunology portfolio.
- Proposing novel targets within the immunology space.
- Ensuring that MR and other causal-inference methods are sound, appropriately caveated, and actionable for non-specialist stakeholders.
- Establishing strong working relationships with target discovery, translational medicine, and external genetics collaborators.
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 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
$153,000 - $246,400
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.
TN Biotech & Pharma Job Roles in Indiana
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Search Biotech & Pharma Jobs in IndianaBiotech & Pharma TN Sponsorship Jobs in Indiana: Frequently Asked Questions
Which biotech & pharma companies sponsor TN visas in Indiana?
Eli Lilly and Company is Indiana's most prominent pharma employer and has sponsored TN visas for scientists, engineers, and regulatory professionals. Other active employers include Cook Medical, Corteva Agriscience, Elanco Animal Health, and Roche Diagnostics. Sponsorship patterns vary by role and business need, so confirming TN eligibility directly with each employer's HR or immigration team is important before applying.
Which cities in Indiana have the most biotech & pharma TN sponsorship jobs?
Indianapolis is the clear center of Indiana's pharma industry, home to Eli Lilly's global headquarters and a concentration of contract research organizations and life sciences suppliers. Bloomington hosts Cook Medical and has a secondary cluster of medical device and biotech employers. West Lafayette, near Purdue University, supports research-oriented roles and early-stage biotech activity with connections to academic spinoffs.
What types of biotech & pharma roles typically qualify for TN sponsorship?
TN visa eligibility in biotech and pharma depends on the specific USMCA occupational category, not just the job title. Roles that commonly qualify include biochemists, chemists, pharmacists, engineers, scientific technicians, and computer systems analysts supporting R&D platforms. The position must require a relevant bachelor's degree or higher in a specific field, and the offered role must align closely with that credential. Regulatory affairs specialists may qualify under certain scientific categories depending on degree background.
How do I find biotech & pharma TN sponsorship jobs in Indiana?
Migrate Mate is a job board built specifically for TN visa holders and applicants, filtering listings by visa type and industry. Searching for biotech and pharma roles in Indiana on Migrate Mate surfaces positions from employers actively open to TN sponsorship, saving time compared to screening general job postings manually. Filtering by the TN category ensures the roles listed are relevant to Canadian and Mexican professionals seeking work authorization.
Are there state-specific or industry-specific considerations for TN sponsorship in Indiana's biotech sector?
Indiana does not impose state-level immigration requirements beyond federal standards, so TN sponsorship follows standard USMCA procedures. Within the biotech and pharma industry, employers in Indiana often work with specialized immigration counsel given the technical nature of qualifying occupations. Roles tied to DEA-regulated substances, such as certain pharmaceutical manufacturing positions, may involve additional federal licensing steps that are separate from but run parallel to the TN process.