Regeneron

AssociateScientist-AssayDevelopment

$70–110k Tarrytown, New York, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Associate Scientist - Assay Development at Regeneron. Skills: Assay development, Immunoassays. Design immunoassays. Execute immunoassays”

Industry & Context.

Problems you'll solve

Troubleshoot assay problems

What They're Looking For.

Must Have

Bachelor or Master degree, 0-3+ years experience, Hands-on immunoassays knowledge, Knowledge of detection systems, Understanding of protein measurement methodologies, Understanding of immunogenicity measurement methodologies

Nice to Have

Prior experience in bioanalytical assay development

What You'll Do.

Troubleshoot assay problems

Perform follow-up experiments

Suggest protocol modifications

Suggest alternative protocols

Develop immunoassay methods

Write assay validation protocols

Work on multiple projects

Perform validation experiments

Write validation reports

Review validation reports

Write procedure documents

Review procedure documents

Communicate effectively

Oversee reagent preparation

Oversee buffer preparation

Coordinate re-ordering supplies

Coordinate re-ordering reagents

Operate laboratory instrumentation

Oversee instrument verifications

Oversee instrument maintenance

Evaluate new technologies

Maintain GLP compliance

Maintain laboratory cleanliness

Comply with safety requirements

Recognize safety problems

Correct safety problems

How You'll Work.

Team & Collaboration

Communicate with supervisor; Work with other scientists

Communication Scope

Verbal reporting; Written reports; Presentations

Full Job Description

Regeneron's Assay Development Group (ADG), located in Tarrytown, NY, is seeking a highly motivated **Associate Scientist** to join the team. The ADG in Bioanalytical sciences develops preclinical and clinical assays to support program pipeline. In this role, you will support ongoing work, sample preparation, assay runs, data processing ensuring compliance with current GxP guidance documentation. **Responsibilities during a typical day might include the following:** * Designs and executes immunoassays (e.g., ELISA) with limited supervision, based on protocols provided by literature, seminars and other scientists. Troubleshoots assay-related problems with minimal guidance of his/her supervisor and performs follow-up experiments. Suggest modifications to protocols or alternative protocols. * Develops immunoassay methods and writes assay validation protocols for review with minimal supervision by supervisor and/or Study Director. * Routinely multi-tasks and can work on multiple projects simultaneously. * Summarizes and presents results to supervisors in a logical manner, verbally and in written reports or presentations. * Performs validation experiments, summarizes results in a tabular manner. Writes/reviews validation reports and procedure documents for review by the Study Director. * Communicate effectively with supervisor and other members of the Assay Development Group. * Oversee the preparation of reagents and buffers for use within the Assay Development Group and may coordinate the re-ordering of laboratory supplies and reagents when needed. * Effectively operates a range of laboratory instrumentation and may oversee instrument verifications and/or maintenance, if required. * May evaluate new technologies for the development of immunoassays using new formats or techniques. * Maintains GLP compliance for all laboratory work and documentation related to assay validations in accordance with FDA regulations and company SOPs. Assists in maintaining GLP compliance in th

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