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Freelance Assay Development Scientist Jobs in Indiana

As the Principal Research Scientist for In Vitro Assay Development, you will be the 'Architect of the Lab Test' for Elanco's research portfolio. You will serve as the scientific hub for a team ...

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 ...

$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 ...

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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Freelance Assay Development Scientist information

What is a freelance assay development scientist?

A Freelance Assay Development Scientist is an independent scientific professional who specializes in designing, optimizing, and validating assays for research, diagnostics, or drug development projects. Unlike in-house scientists, freelancers typically work on a contract basis for multiple clients, providing expertise in assay development across various platforms such as ELISA, PCR, or cell-based assays. Their responsibilities may include troubleshooting existing assays, developing new methodologies, and ensuring that assays meet required sensitivity, specificity, and reproducibility standards. This role requires strong analytical skills, knowledge of relevant technologies, and the ability to work autonomously. Freelance assay development scientists often collaborate remotely with research organizations, biotech companies, and academic institutions.

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

To thrive as a Freelance Assay Development Scientist, you need a strong background in biochemistry, molecular biology, or a related field, often with an advanced degree and practical laboratory experience. Familiarity with analytical instruments (such as HPLC, ELISA, or PCR), data analysis software, and quality control standards is typically required. Excellent problem-solving skills, self-motivation, and effective communication are crucial for managing projects independently and collaborating with clients. These capabilities ensure the development of reliable assays, client satisfaction, and the ability to adapt to varied project requirements in a competitive freelance environment.

What are some common challenges freelance assay development scientists face when managing multiple client projects?

Freelance assay development scientists often juggle several projects with varying requirements and timelines. A common challenge is balancing the need for clear communication with clients while maintaining rigorous documentation and data integrity across different assays. Additionally, freelancers must be adept at troubleshooting unexpected technical issues independently and quickly adapting methods to meet each client's unique specifications. Effective time management and transparent updates are key to building trust and ensuring project success.
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 Freelance Assay Development Scientist jobs in Indiana look for? The top searched job categories for Freelance Assay Development Scientist jobs in Indiana are:

Sr. Quality Control Scientist

Regeneron Pharmaceuticals

Rensselaer, IN • On-site

$78K - $128K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 28 days ago


Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

14th of 86 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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