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Salary
≈ $114k – $215k per year (Estimated)
Location
In office (Rensselaer)
Seniority
Senior · 6+ years exp
Visa
H-1B filings in 12 months: 316 · for this role: 73 · green card filings: 4
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 30, 2026. First seen by Alion on Oct 29, 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

Build our future together:

Regeneron is building the digital Quality Control laboratory and needs a QC scientist who works in data. This role is for someone with hands-on QC laboratory experience who also has strong data and statistics skills. You will validate that what reaches LIMS is exactly what left the instrument, maintain the statistical control limits behind Review by Exception (RBE), and turn QC data into information leaders can act on. Your judgment about analytical and bioassay variability is what makes this role work. You will work across the orchestration layer, LIMS, and instrument software, helping bring Industry 4.0 laboratories into practice. Day to day, you will deliver the QC scientific data framework with strong scientific judgment.

When & where:

  • Monday-Friday, 8:00am-4:30pm
  • Location: Rensselaer, New York, United States

Discover your role:

  • Execute daily validation and reconciliation of instrument-to-LIMS data flows across the lab bus, confirming the completeness, accuracy, and integrity of data transferred from instruments (Empower and others) into LIMS and data lake solutions.
  • Maintain and monitor statistically valid control limits and RBE logic. Triage flags and out-of-trend signals with method-specific scientific judgment and escalate issues.
  • Validate parsing and data-transformation configurations for every new method onboarding, instrument qualification, and software release, ensuring analytical outputs are interpreted correctly before they reach LabWare.
  • Troubleshoot data-transfer discrepancies at the scientific level, distinguishing formatting and rounding artifacts from true signal-integrity issues and drive them to resolution.
  • Build and maintain dashboards, reports, and analytics that turn QC data into actionable information for analysts, managers, and stakeholders.
  • Apply statistical and machine-learning-supported tools (multivariate analysis, trending, anomaly detection) to performance-monitoring programs and technical investigations.
  • Support GMP data integrity (ALCOA+) for the scientific data layer, and contribute to investigations, CAPAs, and inspection readiness.
  • Partner with QC analysts, laboratory informatics/IT, and OT to keep the scientific data pipeline healthy. You lead the scientific and data-quality dimension, while infrastructure and platform administration remain with IT/OT.
  • Use LLMs (Claude, ChatGPT, etc.) to accelerate drafting, coding, and analysis, with the judgment to keep probabilistic AI out of validated GMP data and quality decisions.

This role requires:

  • BS/BA in Biochemistry, Chemistry, Biology, or a related life science, with 6+ years of hands-on QC or analytical laboratory experience, and data and statistics experience in a GMP pharmaceutical or biotechnology setting.
  • A PhD with 2+ years of relevant experience is strongly preferred.
  • Direct experience generating, reviewing, or troubleshooting analytical data from methods such as HPLC/UPLC (Empower), bioassays (cell-based potency, ELISA), or similar release and stability testing.
  • Working knowledge of analytical and bioassay variability, including system suitability, assay controls, and distinguishing true signal from noise.
  • Experience with GMP data integrity (ALCOA+), deviations, investigations, and CAPAs.
  • Applied statistics: trending, control limits, and multivariate methods (PCA/PLS).
  • SQL and Python and/or R for data manipulation.
  • Experience with at least one statistical or modeling tool (JMP, Minitab, SIMCA, Discoverant, MATLAB) and at least one visualization tool (Tableau, Spotfire, Power BI).

Preferred experience:

  • LabWare LIMS experience
  • Anomaly detection and machine-learning exposure
  • ETL, data cleansing, and data-modeling experience

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)

$78,700.00 - $128,700.00
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