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Principal Scientist Assay Development Jobs in Indiana

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Principal Scientist Assay Development information

What does a principal scientist assay development do?

A Principal Scientist in Assay Development leads the design, optimization, and validation of assays used for research, diagnostics, or drug development. They oversee laboratory teams, develop protocols, and ensure that assays meet regulatory and quality standards. Their role also involves troubleshooting complex scientific problems, collaborating with cross-functional teams, and staying current with technological advances in assay technologies. Principal Scientists play a key role in translating scientific concepts into reliable, reproducible assays that support broader organizational goals.

What are some common challenges faced by principal scientists assay development, and how can they be addressed?

Principal Scientists in Assay Development often encounter challenges such as optimizing assay sensitivity and specificity, troubleshooting inconsistent results, and scaling up assays for high-throughput screening. Addressing these issues requires strong analytical thinking, effective cross-functional collaboration with research, engineering, and quality assurance teams, and staying updated with the latest technological advances. Regularly reviewing validation protocols and actively participating in peer discussions can also help in overcoming technical hurdles and ensuring robust assay performance.

What are the key skills and qualifications needed to thrive as a principal scientist assay development, and why are they important?

To thrive as a Principal Scientist Assay Development, you need advanced expertise in biochemistry or molecular biology, a PhD or equivalent experience, and a strong background in assay design and validation. Familiarity with laboratory automation, data analysis software, and regulatory compliance systems such as GLP/GMP is typically required. Leadership, project management, and effective communication are crucial soft skills for guiding teams and collaborating across departments. These skills ensure robust assay performance, regulatory adherence, and efficient innovation in complex scientific environments.

What is the difference between Principal Scientist Assay Development vs Senior Scientist Assay Development?

AspectPrincipal Scientist Assay DevelopmentSenior Scientist Assay Development
CredentialsAdvanced degree (PhD or equivalent), extensive experienceMaster's or PhD, significant industry experience
Work EnvironmentLeads assay development projects, strategic planningExecutes assay development tasks, supports project teams
Employer & Industry UsagePharmaceutical, biotech, CROs, biotech companiesPharmaceutical, biotech, research labs

The main difference between Principal Scientist Assay Development and Senior Scientist Assay Development lies in their level of responsibility and leadership. Principal Scientists typically lead projects, set strategies, and have more extensive experience, while Senior Scientists focus on executing assays and supporting project goals. Both roles require strong technical expertise, but the Principal Scientist position involves higher-level decision-making and oversight.

What job categories do people searching Principal Scientist Assay Development jobs in Indiana look for?

The top searched job categories for Principal Scientist Assay Development jobs in Indiana are:

What cities in Indiana are hiring for Principal Scientist Assay Development jobs?

Cities in Indiana with the most Principal Scientist Assay Development job openings:

Infographic showing various Principal Scientist Assay Development job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution.

Senior Associate Scientist - Plate-Based Analytical Assays - Transitional and Early Development

Indianapolis, IN • On-site

Socket.dev
Network Security • 1 - 10 employees

$90 - $120/hr

Other

Retirement, PTO

Posted 11 days ago


Job description

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!

Senior Associate Scientist – Plate-Based Analytical Assays – Transitional and Early Development About the Role

Senior Associate Scientist in the Transitional and Early Development team, you will play a critical role in bridging early discovery and clinical development for Elanco’s biotherapeutics pipeline. This laboratory-based position focuses on the design, execution, and optimization of research-stage plate-based analytical assays to support the screening and characterization of hit monoclonal antibodies (mAbs) and other complex biomolecules.

You will be responsible for building customized screening assays (including receptor blocking ELISAs, AC‑SINS, and PEG assays) and designing the necessary tool reagents to evaluate early‑stage molecules. Furthermore, you will develop robust quantitative ELISAs for lead molecules, ensuring these methods are phase‑appropriate and ready for seamless tech transfer to Analytical Development once projects approach Pipeline Entry.

Your Responsibilities
  • Perform routine and customized research‑stage plate assays, including receptor blocking ELISAs, quantitative ELISAs, AC‑SINS, and PEG precipitation assays to screen hit mAbs and other biomolecules.
  • Develop, optimize, and qualify quantitative ELISAs for lead candidate molecules. Ensure these assays meet early robustness criteria for successful technology transfer to the Analytical Development team at Pipeline Entry.
  • Proactively design, source, and evaluate critical tool reagents (e.g., capture/detection antibodies, recombinant target proteins) required for customized ligand‑binding assays.
  • Analyze large datasets using appropriate statistical and graphing software (e.g., GraphPad Prism, JMP). Document all experimental work meticulously in electronic lab notebooks (ELN) and author technical reports.
  • Interface daily with scientists across Discovery Research and Analytical Development to ensure assay strategies align with project milestones and molecule characterization needs.
  • Evaluate and implement new plate‑based technologies and high‑throughput automation strategies to improve screening efficiency and data quality.
What You Need to Succeed (Minimum Qualifications)
  • Education:
    • B.S. or M.S. in Immunology, Biochemistry, Molecular Biology, Cell Biology, or a closely related scientific discipline.
  • Experience:
    • B.S. with 4+ years, or M.S. with 2+ years of relevant biopharmaceutical industry experience focusing on assay development and/or early research screening.
  • Technical Skills:
    • Extensive, hands‑on expertise in developing, optimizing, and troubleshooting ligand‑binding assays (especially ELISAs).
    • Demonstrated ability to design and evaluate tool reagents for novel assay development.
    • Strong analytical problem‑solving skills with the ability to learn quickly and assimilate new laboratory techniques.
    • Excellent written and verbal communication skills, with a track record of effective collaboration in a matrixed team environment.
What Will Give You a Competitive Edge (Preferred Qualifications)
  • Direct experience with biophysical/colloidal stability screening assays such as AC‑SINS and PEG precipitation assays.
  • Understanding of the analytical requirements for transitioning early research assays into validate‑able methods for late‑stage Analytical Development and Quality Control.
  • Experience with automated liquid handlers or high‑throughput plate reading platforms to scale early screening efforts.
  • Strong background in protein biochemistry and structural understanding of monoclonal antibodies (mAbs) and multi‑specific biologics.
  • Experience utilizing Design of Experiments (DoE) for assay optimization.
Additional Information:
  • Travel: Minimal
  • Location: Global Elanco Headquarters - Indianapolis, IN - Hybrid Work Environment

Don'tmeet every single requirement? Studies have shown underrecognized groups are less likely to applytojobs 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 butdon'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:
  • 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.

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