Scientist Visa Sponsorship Jobs in Indiana
Indiana's scientist roles are concentrated in life sciences, pharmaceuticals, and agricultural research, with major employers like Eli Lilly, Corteva Agriscience, and Cook Medical headquartered in Indianapolis and surrounding areas. Universities including Purdue and Indiana University also drive significant research hiring. Many of these employers have established records of H-1B visa and O-1 visa sponsorship for qualified scientists.
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Get Access To All JobsAt Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
About the Role
As a Sr. Associate / Consultant Formulation Scientist on the Biopharma Technical Development – Formulations team, you will be a key, hands-on contributor in developing stable and robust formulations and drug product processes for new biological therapeutics. In this laboratory-based role, you will focus on formulation and drug product process development for biopharmaceutical modalities such as monoclonal antibodies, therapeutic proteins, peptides, and other complex biologics.
You will drive the execution of formulation development studies across development stages for sterile injectable and freeze-dried (lyophilized) drug products. You will partner closely with scientists in downstream process development, analytical sciences, and other CMC functions to deliver high-quality formulation and drug product process development packages that enable successful clinical and commercial supply.
Your Responsibilities
- Plan and perform early developability and pre-formulation assessments (e.g., stress testing, formulation screening, and phase-appropriate stability studies) using biophysical and analytical tools (such as DSC, DLS/Zetasizer, particulate analysis, SEC and related techniques) to enable lead candidate and formulation selection.
- Design, plan, and execute formulation and process development studies for biological drug products (e.g., sterile injectables, lyophilized products, multi-dose vials, and other presentations).
- Implement and oversee automated equipment/workflows to improve efficiency.
- Support the manufacturing of materials for early clinical trials by performing aseptic filling, utilizing single-use systems, peristaltic pumps, and small-scale filling assemblies.
- Anticipate and resolve key technical and process-related challenges to meet project timelines and deliverables.
- Analyze complex data sets, draw clear conclusions, and provide timely feedback and recommendations to enable data-driven formulation decisions.
- Document experimental work in electronic lab notebooks and author concise technical reports and presentations to support internal decision-making and, as appropriate, regulatory submissions.
- Collaborate closely with downstream/process development, analytical sciences, device/packaging, manufacturing, and quality teams to translate laboratory findings into robust, scalable drug product processes.
- Contribute to continuous improvement of formulation development workflows, analytical capabilities, and laboratory practices, including evaluation and implementation of new technologies where appropriate.
What You Need to Succeed (Minimum Qualifications)
Education:
- B.S. or M.S. in Pharmaceutical Sciences, Chemistry, Biochemistry, Chemical Engineering, or a related scientific/engineering discipline.
Experience:
- B.S. with 5-7+ years of relevant industry experience, or M.S. with 3+ years of relevant industry experience, in formulation development of biologics or other biopharmaceutical products.
Technical Skills:
- Demonstrated, hands-on experience in formulation development of monoclonal antibodies, therapeutic proteins, peptides, or other biopharmaceutical drug products.
- Familiarity with biophysical and analytical characterization techniques commonly used in biologics formulation (e.g., DSC, DLS/Zetasizer, SEC or related chromatographic methods).
- Hands-on experience with laboratory automation and high-throughput screening platforms, including programming and operating systems.
- Demonstrated experience in aseptic processing and manual/semi-automated filling operations.
- Strong skills in quantitative data analysis, scientific problem-solving, and clear written and verbal scientific communication.
- Comfort working in a highly regulated, quality-focused laboratory environment and following safety, compliance, and data-integrity practices.
What Will Give You a Competitive Edge (Preferred Qualifications)
- Direct experience with multiple dosage forms and presentations (e.g., sterile injectables, lyophilized products, multi-dose vials, pre-filled syringes, or other device-containing presentations).
- Direct experience developing freeze-dried formulations and lyophilization cycles.
- Proven technical agility and a track record of proactively identifying and solving complex formulation or process challenges.
- Experience using statistical tools (e.g., JMP or similar) for design of experiments (DoE) and data analysis.
- Prior experience collaborating on cross-functional CMC teams and/or supporting technology transfer to clinical or commercial manufacturing sites.
- Demonstrated interest in innovation and continuous improvement (e.g., implementation of new biophysical methods, automation, or digital data workflows).
Additional Information
Location: Global Elanco Headquarters – Indianapolis, IN (Hybrid Work Environment)
Travel: Minimal (e.g., occasional travel to development or manufacturing sites)
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
- Multiple relocation packages
- Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
- 8-week parental leave
- 9 Employee Resource Groups
- Annual bonus offering
- Flexible work arrangements
- Up to 6% 401K matching
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
About the Role
As a Sr. Associate / Consultant Formulation Scientist on the Biopharma Technical Development – Formulations team, you will be a key, hands-on contributor in developing stable and robust formulations and drug product processes for new biological therapeutics. In this laboratory-based role, you will focus on formulation and drug product process development for biopharmaceutical modalities such as monoclonal antibodies, therapeutic proteins, peptides, and other complex biologics.
You will drive the execution of formulation development studies across development stages for sterile injectable and freeze-dried (lyophilized) drug products. You will partner closely with scientists in downstream process development, analytical sciences, and other CMC functions to deliver high-quality formulation and drug product process development packages that enable successful clinical and commercial supply.
Your Responsibilities
- Plan and perform early developability and pre-formulation assessments (e.g., stress testing, formulation screening, and phase-appropriate stability studies) using biophysical and analytical tools (such as DSC, DLS/Zetasizer, particulate analysis, SEC and related techniques) to enable lead candidate and formulation selection.
- Design, plan, and execute formulation and process development studies for biological drug products (e.g., sterile injectables, lyophilized products, multi-dose vials, and other presentations).
- Implement and oversee automated equipment/workflows to improve efficiency.
- Support the manufacturing of materials for early clinical trials by performing aseptic filling, utilizing single-use systems, peristaltic pumps, and small-scale filling assemblies.
- Anticipate and resolve key technical and process-related challenges to meet project timelines and deliverables.
- Analyze complex data sets, draw clear conclusions, and provide timely feedback and recommendations to enable data-driven formulation decisions.
- Document experimental work in electronic lab notebooks and author concise technical reports and presentations to support internal decision-making and, as appropriate, regulatory submissions.
- Collaborate closely with downstream/process development, analytical sciences, device/packaging, manufacturing, and quality teams to translate laboratory findings into robust, scalable drug product processes.
- Contribute to continuous improvement of formulation development workflows, analytical capabilities, and laboratory practices, including evaluation and implementation of new technologies where appropriate.
What You Need to Succeed (Minimum Qualifications)
Education:
- B.S. or M.S. in Pharmaceutical Sciences, Chemistry, Biochemistry, Chemical Engineering, or a related scientific/engineering discipline.
Experience:
- B.S. with 5-7+ years of relevant industry experience, or M.S. with 3+ years of relevant industry experience, in formulation development of biologics or other biopharmaceutical products.
Technical Skills:
- Demonstrated, hands-on experience in formulation development of monoclonal antibodies, therapeutic proteins, peptides, or other biopharmaceutical drug products.
- Familiarity with biophysical and analytical characterization techniques commonly used in biologics formulation (e.g., DSC, DLS/Zetasizer, SEC or related chromatographic methods).
- Hands-on experience with laboratory automation and high-throughput screening platforms, including programming and operating systems.
- Demonstrated experience in aseptic processing and manual/semi-automated filling operations.
- Strong skills in quantitative data analysis, scientific problem-solving, and clear written and verbal scientific communication.
- Comfort working in a highly regulated, quality-focused laboratory environment and following safety, compliance, and data-integrity practices.
What Will Give You a Competitive Edge (Preferred Qualifications)
- Direct experience with multiple dosage forms and presentations (e.g., sterile injectables, lyophilized products, multi-dose vials, pre-filled syringes, or other device-containing presentations).
- Direct experience developing freeze-dried formulations and lyophilization cycles.
- Proven technical agility and a track record of proactively identifying and solving complex formulation or process challenges.
- Experience using statistical tools (e.g., JMP or similar) for design of experiments (DoE) and data analysis.
- Prior experience collaborating on cross-functional CMC teams and/or supporting technology transfer to clinical or commercial manufacturing sites.
- Demonstrated interest in innovation and continuous improvement (e.g., implementation of new biophysical methods, automation, or digital data workflows).
Additional Information
Location: Global Elanco Headquarters – Indianapolis, IN (Hybrid Work Environment)
Travel: Minimal (e.g., occasional travel to development or manufacturing sites)
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
- Multiple relocation packages
- Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
- 8-week parental leave
- 9 Employee Resource Groups
- Annual bonus offering
- Flexible work arrangements
- Up to 6% 401K matching
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
Scientist Job Roles in Indiana
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Search Scientist Jobs in IndianaScientist Jobs in Indiana: Frequently Asked Questions
Which companies sponsor visas for scientists in Indiana?
Eli Lilly is among the most active sponsors, particularly for pharmaceutical research scientists. Corteva Agriscience regularly sponsors agricultural and biological scientists, while Cook Medical hires research-focused roles. Dow AgroSciences (now part of Corteva) and Indiana University Health also appear in federal Labor Condition Application filings for scientist positions. Sponsorship activity is concentrated in life sciences, agriscience, and medical device research.
Which visa types are most common for scientist roles in Indiana?
The H-1B is the most common visa for scientists in Indiana, as most research and laboratory roles qualify as specialty occupations requiring at least a bachelor's degree in a specific scientific field. Scientists with exceptional credentials may qualify for the O-1A, which requires demonstrated extraordinary ability. Postdoctoral researchers at Indiana universities often enter on J-1 visa exchange visitor visas through institutional sponsorship programs.
How to find scientist visa sponsorship jobs in Indiana?
Migrate Mate filters scientist job listings specifically to employers with a history of visa sponsorship in Indiana, saving you from manually reviewing hundreds of postings. You can search by role type, city, and visa category to surface relevant openings at employers like Eli Lilly, Corteva, and Indiana university research centers. This is particularly useful for narrowing down pharmaceutical, agricultural science, and biomedical research positions.
Which cities in Indiana have the most scientist sponsorship jobs?
Indianapolis accounts for the largest share, driven by Eli Lilly's headquarters and a concentration of pharmaceutical and biotech employers in the metro area. West Lafayette is significant due to Purdue University's extensive research programs and affiliated industry partners. Bloomington sees activity tied to Indiana University and its life sciences research infrastructure. Indianapolis's Indy BioCrossroads initiative has also helped attract additional research employers to the region.
Are there state-specific considerations for scientists seeking sponsorship in Indiana?
Indiana's prevailing wage requirements for H-1B positions are set by the Department of Labor based on the specific occupation and geographic area, so wages for scientists in Indianapolis may differ from rural Indiana counties. Purdue University and Indiana University serve as notable pipelines, with international graduates in chemistry, biology, and materials science frequently transitioning to employer-sponsored roles at nearby industry partners after completing OPT or CPT.
What is the prevailing wage for sponsored scientist jobs in Indiana?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.