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Sr. Associate​/Consultant Formulation Scientist - Biopharma

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: Indiana Ag Connection
Full Time position
Listed on 2026-10-18
Job specializations:
  • Research/Development
    Pharmaceutical Science/ Research, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 110000 - 170000 USD Yearly USD 110000.00 170000.00 YEAR
Job Description & How to Apply Below
Position: Sr. Associate / Consultant Formulation Scientist - Biopharma
Location: Indianapolis

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** 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 develop ability 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…
Position Requirements
10+ Years work experience
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