Regeneron's Assay Development Group (ADG), located in Tarrytown NY, is seeking an energetic Sr Scientist. In this exciting role, you will critically evaluate ongoing processes and suggest improvements, especially those that ensure compliance with current GxP guidance documentation.

A Typical Day in the Role of Sr. Scientist might look like:Independently design, perform, complete and troubleshoot immune-assays (e.g., ELISA) based on protocols provided by literature, supervisor and other scientistsDevelop and optimize sophisticated genomic assays and immunoassays (i.e. PK, biodistribution, PD and ADA) with minimal guidanceRoutinely perform multiple assays within the same day and works on multiple projects simultaneouslySummarizes and presents results to supervisor in a logical manner, verbally and in written reports. Delivers presentations related to project assignments within department and to cross functional departments. May present data to senior management. Communicates effectively with supervisor and other personnel within ADG. Anticipates and discusses reagent needs and/or services with outside vendors. Interacts with other groups within the company on specific projects to discuss ADG deliverables.Reads and critically evaluates literature related to project assignments. Applies concepts to experimental design. Stays current on relevant regulatory guidance and best practice documents for ligand binding, biomarker and immunogenicity assays.Identify and independently evaluate new technologies for the development of assays using new formats or techniques.Write assay validation protocols, validation reports and bioanalytical method procedures with few or no subsequent edits for review by supervisor and/or Study DirectorTakes the lead/supervisory role in planning of validation experiments and securing resources and reagents for validationMay independently train on validated bioanalytical methods and perform sample analysis, if neededMay function as Study Director for assay validation studies conducted by others. May supervise Laboratory Assistants, R&D Associates, and/or R&D SpecialistsMaintain GLP compliance for all laboratory work and documentation related to assay validations in accordance with FDA regulations and company SOPsEnsure GLP compliance is maintained in the laboratory

This Role May Be for You If:You have strong initiative and drive to complete ambitious tasks and learn new technologies.You are capable of multi-tasking, working both independently and within a team environment.

This role requires a Doctorate Degree (Ph.D) in biology or a related field and a minimum of 3+ years of relevant post-doctoral experience. Experience in AAV-based gene therapies with a focus on development of novel bioanalytical assay platforms to support nonclinical and clinical is highly desirable. Hands-on knowledge in immunoassays a plus. Strong understanding of regulatory landscape for assays supporting bioanalytical assessments for viral-based gene delivery support Immunology/immunogenicity expertise (both highly developed and adaptive) a plus. Experience in a cGXP environment preferred.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions.  For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process.  Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (annually)

$108,300.00 - $176,700.00