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Salary
$62k – $92k per year
Location
In office (United States)
Seniority
Junior · 2+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 29, 2026. First seen by Alion on Oct 28, 2026. Regeneron Pharmaceuticals scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Headquartered in Tarrytown, New York, United States, Regeneron Pharmaceuticals is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases. The company accelerates traditional drug development using proprietary technologies, such as VelociSuite, alongside advanced genetic sequencing to uncover novel biological insights. Supported by a robust research and development pipeline, its innovative therapeutics provide proven treatments for patients suffering from cancer, eye diseases, inflammatory disorders, and rare conditions.
Backed by GV, venBio Partners

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Analytical Scientist to join our Quality Control team in Rensselaer, NY, supporting our IOPS organization on-site. In this role, you will shape the future of QC analytical testing by designing, developing, and scaling automated assay workflows across advanced laboratory platforms. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where

Location: Rensselaer, NY (Tempel Lane)

Work Shift: Monday-Friday 1st shift

Discover your role:

  • Design, implement, and optimize automated assay workflows across modern laboratory platforms, applying expertise in mass spectrometry, chromatography, bioassay, electrophoresis, and ELISA.
  • Set priorities, coordinate work, and track progress on analytical and automation initiatives against key milestones.
  • Design and execute studies to evaluate emerging automation technologies and troubleshoot existing systems with some to limited supervision.
  • Lead complex investigations into automated method performance, supporting verification activities and driving continuous improvement.
  • Transfer automated workflows to QC and partner functions by developing training materials, transfer plans, and acceptance criteria.
  • Engage cross-functional collaborators and equipment vendors to evaluate new technologies and assess their fit for QC applications.
  • Prepare clear scientific reports, automation procedures, and SOPs; communicate findings, risks, and mitigation strategies to management and cross-functional teams.
  • Bring hands-on experience programming and optimizing automated liquid handling systems (e.g., Hamilton/Venus, Andrew+/OneLab, or Cellario) and scripting in Python, R, or VBA.
  • Apply strong troubleshooting skills across both analytical methods and automated instrumentation to resolve complex technical challenges.
  • Make sound, independent decisions and proactively recommend experiments or solutions based on expertise in analytical science and automation.

This role requires:

  • 2+ years of industry experience in analytical development, laboratory automation, and QC method lifecycle management (or equivalent combination of education and experience).
  • Demonstrated hands-on expertise in automated liquid handling platforms and associated software programming.
  • Experience in scripting languages (Python, R, or VBA) for data analysis, workflow automation, or system integration.
  • Knowledge of QC analytical techniques including mass spectrometry, chromatography, electrophoresis, bioassay, or ELISA.
  • Proven ability to work independently, design scientifically sound studies from broad objectives, and drive projects to completion.
  • Level will be determined based on qualifications at the time of offer.

Preferred:

  • B.S./B.A. or higher in Chemistry, Biochemistry, Biology, or a related field.
  • Previous experience working in a cGMP or cGLP regulated environment.
  • Familiarity with Cellario, Venus (Hamilton), or OneLab (Andrew+) automation platforms.

Physical Requirements: Ability to work in a laboratory environment, including standing for extended periods and handling laboratory equipment.

Gowning & Environment: This role operates in a GMP analytical laboratory. Appropriate gowning and PPE are required in designated areas.

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 on-site. Please speak with your recruiter and hiring manager for more information about on-site 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)

$62,355.00 - $92,400.00
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