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Full Time Assay Development Scientist Jobs in Indiana

You will partner with discovery and development scientists to build machine learning and ... assay, imaging, behavioral) to deliver reliable predictions and classifications. * Shape data ...

Environmental Fate Scientist

Indianapolis, IN · On-site

$71K - $94K/yr

This role is also responsible for the development and implementation of new laboratory assays to ... The successful candidate will serve as an Efate scientist in the screening and characterization of ...

Materials Engineer

New Albany, IN · On-site

$85K - $120K/yr

The Materials Scientist will be responsible for developing innovative solutions using various ... Maintain accurate and timely records of experimental designs, assay development, experimental ...

Located in Indianapolis, IN, our scientists have access to world-class pharmaceutical development ... Support the transfer of potency assays for QC release and stability testing to meet product and ...

New

Biologist

Indianapolis, IN · On-site

$65K - $169K/yr

... assay development and implementation supporting discovery efforts and clinical studies ... We are seeking a highly motivated scientist to join Reagents Group. This role is a part of a multi ...

Biologist

Indianapolis, IN · On-site

$65K - $169K/yr

... assay development and implementation supporting discovery efforts and clinical studies ... We are seeking a highly motivated scientist to join Reagents Group. This role is a part of a multi ...

Showing results 21-40

Full Time Assay Development Scientist information

What is a full time assay development scientist?

A Full Time Assay Development Scientist is a laboratory professional who specializes in designing, developing, and optimizing analytical assays for various scientific applications, such as drug discovery, diagnostics, or quality control. They work in research and development teams, conducting experiments, analyzing data, and troubleshooting assay protocols to ensure accuracy and reliability. Their role also involves documenting results, validating new methods, and collaborating with other scientists to support project goals. Typically, they have advanced degrees in biology, chemistry, or related fields and possess strong problem-solving and technical skills.

What are the key skills and qualifications needed to thrive as a full time assay development scientist?

To thrive as a Full Time Assay Development Scientist, you need a strong background in biochemistry, molecular biology, or a related field, typically with an advanced degree (M.S. or Ph.D.) and experience in assay design and optimization. Familiarity with laboratory techniques such as ELISA, PCR, and data analysis software, as well as experience with laboratory information management systems (LIMS), is often required. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for collaborating with cross-functional teams and troubleshooting experiments. These skills are crucial for ensuring the development of robust, reliable assays that advance research and product development objectives.

What are some common challenges faced by full time assay development scientists during the transition from research to routine clinical or commercial assays?

Full Time Assay Development Scientists often encounter challenges when translating laboratory protocols into robust assays suitable for routine clinical or commercial use. These challenges can include optimizing assay reproducibility, ensuring consistent performance across different sample types, and meeting regulatory requirements. Scientists also need to collaborate closely with quality assurance, manufacturing, and regulatory teams to validate and document procedures. Overcoming these hurdles requires strong problem-solving skills, attention to detail, and effective cross-functional communication.

What is the difference between Full Time Assay Development Scientist vs Research Associate?

AspectFull Time Assay Development ScientistResearch Associate
CredentialsBachelor's or Master's in Life Sciences, relevant experienceBachelor's or Master's in Life Sciences, entry-level experience
Work EnvironmentLaboratories focused on assay development and validationResearch labs supporting various projects, often assisting assay teams
Industry UsageCommon in biotech, pharma, and diagnostics companiesUsed across research institutions and biotech firms

The Full Time Assay Development Scientist typically has more specialized experience in designing and validating assays, working independently on development projects. In contrast, the Research Associate often supports research activities, assisting assay development under supervision. Both roles are essential in biotech and pharma industries, but the Scientist role involves greater responsibility and expertise in assay creation and optimization.

What are the most commonly searched types of Assay Development Scientist jobs in Indiana?

The most popular types of Assay Development Scientist jobs in Indiana are:

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

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

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

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

Infographic showing various Full Time Assay Development Scientist job openings in Indiana as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Sr. Scientist / Principal Scientist, Global Sample Management

Eli Lilly and Company

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical


Job description

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.
Position Summary
At Lilly, the molecules that become medicines start as ideas, and behind every breakthrough is a team that ensured the right compound reached the right assay at the right time. The work of Global Sample Management (GSM) is foundational to drug discovery, and the people who do it well make science move faster.
The Sr. Scientist / Principal Scientist within Global Sample Management executes daily sample management operations while taking active ownership of the data behind that work. This role requires strong information management abilities and effective communication skills to ensure clear sharing and interpretation of information within the Discovery team. The focus is on operationalizing and enhancing Sample Management, which involves improving and building processes for maintaining and distributing various sample types and responding to evolving scientific needs while improving operational efficiency.
Over time, this role may grow more towards data stewardship or operational focus depending on the individual and organizational needs. The level of appointment will be determined by the experience and qualifications of the selected candidate.
Responsibilities
  • Support manual and automated workflows from registration to powder handling through preparation of assay-ready plates and format compound libraries using automated liquid handling and acoustic dispensing instrumentation (e.g., Echo, Hamilton) following established protocols; apply care and consistency to ensure outputs are fit for purpose.
  • Design and enhance workflows for sample storage, manual and automated powder handling operations, liquid handling, ensuring high standards of scientific excellence and integrity.
  • Support instrument qualification, routine maintenance, and basic troubleshooting of laboratory equipment; log maintenance activities accurately and escalate issues to appropriate personnel as needed.
  • Build scientific understanding of assigned sample types and their handling requirements, including how physicochemical properties, storage conditions, and registration accuracy collectively determine whether a compound is fit for assay.
  • Actively engage with scientific project teams to understand the research context behind sample requests, building scientific relationships and situational awareness to become a key scientific partner across Molecule Discovery.
  • Serve as steward for both physical inventory and its associated data, acting as the technical resource for compound registration and data governance across GSM's LIMS platforms.
  • Troubleshoot and resolve complex issues related to software, hardware, and sample dispensing, applying creative problem-solving skills and technical expertise.
  • Develop, test, and validate updates to software, hardware, and procedures, proactively recommending and implementing usability and efficiency improvements to drive scientific progress.
  • Perform quality checks on inbound and outbound samples; resolve deviations from quality guidelines before material ships or is used.
  • Coordinate sample shipments across the GSM network and externally, maintaining proper documentation, chain of custody, and regulatory compliance.
  • Collaborate with informatics, IT, scientific, and operational partners to ensure GSM's data systems meet evolving research requirements; build relationships that enable proactive identification of data risks and opportunities for system improvement.
  • Support the material restriction processes and controlled substance tracking within assigned scope; escalate compliance risks to appropriate stakeholders with clear documentation.
  • Develop and maintain SOPs, governance documentation, and training materials for registration, data, and operational workflows.

Basic Requirements
  • BS or MS in Chemistry, Biology, Pharmaceutics, Informatics, Engineering, Logistics or a related field.
  • 3-5+ years of relevant laboratory or sample management or data stewardship experience.
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1

Additional Skills and Preferences
  • Strong organizational skills with attention to detail across both bench and data workflows.
  • Commitment to data and sample quality as a scientific responsibility.
  • Hands-on experience with LIMS platforms for sample management or similar; ability to identify and resolve data integrity issues across complex, high-volume datasets.
  • Clear communicator; able to work collaboratively and escalate issues with appropriate context.
  • Hands-on experience with automated liquid handling or acoustic dispensing platforms (e.g., Echo, Hamilton, Tecan).
  • Experience handling diverse material types in a high-throughput laboratory environment.
  • Basic SQL skills; interest in building data querying and reporting capability in an operational context.
  • Coursework or practical exposure in cheminformatics or scientific databases relevant to compound identity and registration.
  • Compound or biological sample management experience across one or more modalities.
  • Knowledge of logistics for research materials.
  • Familiarity with OEB/PHM compound potency classifications or high-potency material handling.
  • Awareness of controlled substance handling requirements.

Additional Information:
  • This is an onsite (5 days), lab-based position based in Indianapolis, IN

Work Environment:
The work environment characteristics described are representative of those an employee encounters while performing the essential functions of this job in a laboratory setting.
To perform this job successfully, an individual must be able to perform the role and responsibilities satisfactorily.
Physical Demands:
The physical demands of this job include safe handling of controlled substances and the use of required personal protective equipment.
The physical demands here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
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 (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
$65,250 - $169,400
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.
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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876