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Full Time Assay Development Scientist Jobs in Indiana

Experience with the development and validation of immunogenicity (Anti-Drug Antibody, ADA) assays ... Excellent problem-solving abilities and a high degree of scientific rigor. Elanco is an EEO ...

Serve as a scientific resource for complex data interpretation, assay development, and problem solving * Collaborate with project teams and interact with clients to discuss scientific principles and ...

Biologist II

Indianapolis, IN · On-site

$26 - $28/hr

Identify published scientific evidence to perform and refine early assay development. * Accurate record keeping and reporting of data adhering to client note booking policy. * Good communication ...

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Full Time Assay Development Scientist information

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

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 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 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 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 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 July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.
Sr. Quality Control Scientist

Sr. Quality Control Scientist

Regeneron Pharmaceuticals

Rensselaer, IN • On-site

$78K - $128K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

12th of 74 rated pharmaceutical


Job description

Regeneron is looking for a Sr Quality Control Scientist in the Technical Resources Department. In this position you will perform assay development, characterization, optimization, transfer, validation, and investigations for QC. You would provide technical support, guidance and supervision for release, stability, and in-process testing and assay development.

As a Sr QC Scientist for Chemistry in the Technical Resources Department, a typical day might include the following:

  • Performs assay development/validation for QC.
  • Reviews new test procedures and assays.
  • Evaluates and bring in new methodologies/techniques when needed.
  • Facilitate assay transfer from R&D and to business partners
  • Organize analytical assay transfer internally and externally.
  • Set product specification.
  • Participates in technical troubleshooting and problem investigation.
  • Review analytical development report, assay and process validation report and other technical documents for technical correctness and regulatory compliance.
  • Participates in training programs for analysts.

This job might be for you if:

  • You have in-depth knowledge with HPLC based assays.
  • You like dealing with technical issues, troubleshooting, and constant change
  • You are a team player who can work with a variety of different people on different tasks
  • You have strong written and verbal communication skills
  • You enjoy mentoring and training others on systems, processes and problem solving
  • You enjoy working in a fast-paced environment and are flexible to changing requirements
  • You can take on new and sometimes ambiguous challenges and learn quickly

To be considered for a Sr QC Scientist (Chemistry) Technical Resources role you must have a BS in Chemistry, Biochemistry, Biology, or a related field, and 6+ years of relevant experience. Experience with cell or gene therapy in a Biopharmaceutical environment is strongly preferred.

PhD is preferred.

Level is determined based on experience relevant to the role.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$78,700.00 - $128,700.00

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