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Temporary Assay Development Scientist Jobs in Indiana

Method and Assay Development What You'll Bring: * BS in Biology, Microbiology, Biochemistry or a related science * 0-2+ years of related lab experience * Mammalian Cell Culture experience * RNA/DNA ...

Method and Assay Development What You'll Bring: * BS in Biology, Microbiology, Biochemistry or a related science * 0-2+ years of related lab experience * Mammalian Cell Culture experience * RNA/DNA ...

Cell Biologist II

Indianapolis, IN · On-site

$25 - $28/hr

They will also support assay development which is a key role to identify active compounds: screen ... Receive tasks and information from scientist in charge regarding changes in processes, priorities ...

$25 - $28/hr

They will also support assay development which is a key role to identify active compounds: screen ... Receive tasks and information from scientist in charge regarding changes in processes, priorities ...

$25 - $28/hr

They will also support assay development which is a key role to identify active compounds: screen ... Receive tasks and information from scientist in charge regarding changes in processes, priorities ...

Cell Biologist II

Indianapolis, IN · On-site

$25 - $28/hr

They will also support assay development which is a key role to identify active compounds: screen ... Receive tasks and information from scientist in charge regarding changes in processes, priorities ...

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 ...

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Temporary Assay Development Scientist information

What does an assay development scientist do?

An assay development scientist designs, optimizes, and validates laboratory tests to measure specific biological or chemical substances. They work with techniques such as ELISA, PCR, or spectrophotometry, often using specialized equipment and following regulatory standards to ensure assay accuracy and reliability.

What is assay development in biotech?

Assay development in biotech involves creating and optimizing laboratory tests to measure specific biological or chemical properties, such as the presence or activity of a substance. A Temporary Assay Development Scientist designs, validates, and implements these assays, often using techniques like ELISA, PCR, or spectrophotometry, to support research and product development. This process requires attention to accuracy, reproducibility, and regulatory compliance.

What is the difference between Temporary Assay Development Scientist vs Temporary Quality Control Analyst?

AspectTemporary Assay Development ScientistTemporary Quality Control Analyst
CredentialsBachelor's or Master's in Life Sciences, relevant lab experienceBachelor's in Life Sciences, laboratory experience in quality testing
Work EnvironmentResearch labs, product development teamsQuality control labs, manufacturing support
Industry UsageBiotech, pharmaceutical R&DManufacturing, pharmaceutical QC
Common Search IntentUnderstanding assay development rolesQuality testing and compliance roles

The Temporary Assay Development Scientist focuses on creating and optimizing laboratory assays for new products, often working in R&D settings. In contrast, the Temporary Quality Control Analyst primarily performs testing to ensure products meet quality standards during manufacturing. Both roles require laboratory experience but differ in their focus—development versus quality assurance—making them distinct yet related positions within the biotech and pharmaceutical industries.

What does an analytical development scientist do?

An analytical development scientist designs, optimizes, and validates laboratory methods to analyze biological or chemical samples, ensuring accuracy and reproducibility. They often work with techniques such as chromatography, spectroscopy, and assay development, supporting product development and regulatory submissions in a laboratory setting.

What are the key skills and qualifications needed to thrive as a Temporary Assay Development Scientist, and why are they important?

To thrive as a Temporary Assay Development Scientist, you generally need a degree in biology, chemistry, or a related field, with experience in assay design, optimization, and validation. Familiarity with laboratory instrumentation, data analysis software, and experience with techniques such as ELISA, PCR, or cell-based assays is typically required. Strong problem-solving abilities, attention to detail, and effective collaboration and communication skills distinguish top performers in this role. These skills ensure reliable assay results, support project timelines, and contribute to the overall success of scientific research and product development.

What are Temporary Assay Development Scientists?

Temporary Assay Development Scientists are professionals hired on a short-term basis to design, optimize, and validate laboratory assays, often for use in research, diagnostics, or pharmaceutical development. Their main role is to ensure that assays are reliable, reproducible, and meet the required standards for scientific or regulatory purposes. These scientists typically work in laboratory settings and may collaborate with other scientists or departments to support ongoing projects. Temporary positions may last from a few months to a year, depending on project needs and funding.

What is the highest paying type of scientist?

Among scientists, those in specialized fields such as petroleum engineering, data science, and pharmaceutical research tend to have the highest salaries. Temporary assay development scientists typically earn competitive wages within the biotech and pharmaceutical industries, but generally do not reach the top salary levels of highly specialized or executive roles in science. Salary levels depend on experience, location, and industry demand.

What are some common challenges faced by Temporary Assay Development Scientists, and how can they be managed?

Temporary Assay Development Scientists often encounter challenges such as adapting quickly to new laboratory environments, meeting tight project deadlines, and mastering proprietary protocols unique to each organization. Since the role is temporary, there may be limited time to familiarize oneself with existing workflows and team dynamics. Proactively communicating with colleagues, being organized, and seeking clarification early on can help overcome these hurdles. Staying adaptable and open to feedback is key to succeeding in this fast-paced, collaborative setting.
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:
Director, Molecular Pharmacology

Director, Molecular Pharmacology

Eli Lilly and Company

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

10th of 74 rated pharmaceutical


Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Overview
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you can also count on us to develop creative solutions to support communities through philanthropy and volunteerism.
The Lilly Small Molecule Design group is an organization purpose-built to create molecules that make life better for people. We focus on using cutting-edge science to unlock new approaches that can treat people suffering from diseases with poor treatment options. We continually challenge ourselves to deliver molecules that can provide breakthrough efficacy with the highest possible safety margins. We are dedicated to optimizing our mindset, technology, and processes for faster, more nimble execution. Our success is built on a culture that empowers innovative problem-solving through open collaboration and individual accountability.
Position Summary
The Advanced Molecule Design team's mission is to optimize lead molecules to strong drug candidates that become breakthrough medicines. We are searching for experienced and engaged scientific experts who are recognized authorities in their area of focus and drive the advancement of our portfolio across oncology, immunology, pain, Alzheimer's, diabetes, and obesity. These positions are for seasoned drug hunters who ask the right scientific questions and collect high-impact data to drive projects forward. To be successful, these experts will provide deep scientific knowledge across multiple programs or therapeutic areas, build capabilities that enhance Molecular Pharmacology's impact on the portfolio, and help deliver quality drug candidates to IND. We are looking for innovative scientists with a strong growth mindset who can challenge dogma and champion breakthrough approaches.
Key Responsibilities
  • Design, develop, and execute molecular pharmacology assays and flow schemes to support drug discovery programs, with emphasis on:- 1) Radioligand binding (competition, saturation, kinetic assays, autoradiography) 2) GPCR internalization and receptor trafficking assays and 3) Imaging-based assays including confocal microscopy and/or high content screening (HCS)
  • Develop novel, fit-for-purpose assay platforms from the ground up, including assay design, reagent optimization, cell line selection/engineering, and qualification for drug discovery use
  • Characterize compound pharmacology and mechanisms of action including receptor affinity, selectivity, and functional activity (e.g., G protein signaling, arrestin recruitment, receptor desensitization)
  • Serve as a recognized expert in their field, providing scientific leadership that shapes program strategy and builds credibility across the organization.
  • Provide expert scientific guidance that shapes project strategy and improves probability of technical success across multiple programs or therapeutic areas.
  • Identify capability gaps and develop solutions that benefit multiple programs across the portfolio.
  • Actively incorporate state-of-the-art methods and technologies
  • Incorporate AI/ML into scientific workflows.
  • Foster an environment that supports open scientific debate and bold, evidence-based decisions.
  • Actively mentor and develop diverse scientific talent across sites and functions.
  • Lead cross-functional initiatives that leverage diverse perspectives to drive program outcomes.
  • Champion a ONE TEAM, SAME TEAM mindset; model radical transparency in surfacing challenges.
  • Identify and contribute to external innovation opportunities that strengthen the portfolio.
  • Build internal and external networks that enhance the capabilities of the Molecular Pharmacology team.

Basic Requirements
  • PhD with a minimum of 5+ years of drug discovery experience in the pharmaceutical industry (including academic and post-doc experience); or BS/MS with 10+ years of equivalent experience.
  • Degree in Biochemistry, Biology, Biophysics, Molecular Biology, Pharmacology, or related fields.

Additional Preferences
  • Demonstrated expertise in molecular pharmacology assay development, including radioligand binding and/or imaging-based modalities
  • Demonstrated drug hunter experience with a track record of advancing discovery programs.
  • Deep scientific background in biochemistry, biophysics, and cell biology to guide compound optimization across modalities.
  • Strong experience leading teams of scientists and achieving cross-disciplinary goals.
  • Team player with a positive, can-do attitude and a commitment to scientific rigor and integrity.
  • Hands-on experience with radioligand binding techniques: competition binding, saturation binding, membrane-based assays, and autoradiography support in drug discovery contexts
  • Experience with GPCR internalization and receptor trafficking assays, including one or more of the following: SNAP/CLIP, FRET, luminescence reporters
  • Expertise in receptor pharmacology across multiple target families, with particular emphasis on GPCR downstream signaling
  • Proficiency in confocal microscopy for quantitative cell biology applications: subcellular localization, receptor internalization, endosomal trafficking, colocalization analysis, and live-cell imaging
  • Experience with high content screening (HCS) platforms (e.g., Operetta, Cellomics, IN Cell Analyzer, or equivalent) for automated image acquisition and analysis, including quantification
  • Familiarity with engineered cell line systems
  • Familiarity with CNS or metabolic disease target biology
  • Broad experience across multiple biological mechanisms, modalities, and therapeutic areas.
  • Track record of scientific productivity demonstrated through publications, patents, or internal drug discovery contributions
  • Project or program leader experience is a plus.

Physical Demands / Travel
The physical demands here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Work Environment
This is an onsite position.
This role requires up to 2 days working in the lab.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.
*To perform this job successfully, an individual must be able to perform the role and responsibilities satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
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 Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$148,500 - $257,400
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