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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Principal Analytical Scientist - Automation

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRensselaer, NY, USA$92.2k - $150.6k /yr

About the Job

Requirements

  • The role requires 8 or more years of industry experience in analytical development, laboratory automation, and quality control method lifecycle management, or an equivalent combination of education and experience.
  • Demonstrated hands-on expertise in automated liquid handling platforms and associated software programming is required.
  • Proficiency in scripting languages such as Python, R, or VBA for data analysis, workflow automation, or system integration is required.
  • Deep knowledge of quality control analytical techniques, including mass spectrometry, chromatography, electrophoresis, bioassay, or ELISA, is required.
  • Ability to work independently, design scientifically sound studies from broad objectives, and drive projects to completion is required.
  • Ability to work in a laboratory environment, including standing for extended periods and handling laboratory equipment, is required.
  • Appropriate gowning and personal protective equipment are required in designated areas of the GMP analytical laboratory.

Responsibilities

  • Lead the design, implementation, and optimization of automated assay workflows across modern laboratory platforms, applying expertise in mass spectrometry, chromatography, bioassay, electrophoresis, and ELISA.
  • Mentor and develop junior and mid-level scientists, building team capability in analytical science and laboratory automation.
  • Set priorities, coordinate work, and track progress on analytical and automation initiatives against key milestones.
  • Independently design and execute studies to evaluate emerging automation technologies and troubleshoot existing systems with limited supervision.
  • Lead complex investigations into automated method performance, support verification activities, and drive continuous improvement.
  • Transfer automated workflows to quality control 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 suitability for quality control applications.
  • Prepare scientific reports, automation procedures, and standard operating procedures; communicate findings, risks, and mitigation strategies to management and cross-functional teams.
  • Program and optimize automated liquid handling systems such as Hamilton/Venus, Andrew+/OneLab, or Cellario, and write scripts in Python, R, or VBA.
  • Troubleshoot analytical methods and automated instrumentation to resolve complex technical challenges.
  • Make independent decisions and recommend experiments or solutions based on expertise in analytical science and automation.

Desired Qualifications

  • A PhD in Chemistry, Biochemistry, Biology, or a related field is preferred.
  • Previous experience working in a cGMP- or cGLP-regulated environment is preferred.
  • Familiarity with Cellario, Venus (Hamilton), or OneLab (Andrew+) automation platforms is preferred.
  • Experience developing and executing technology transfer plans across quality control or partner functions is preferred.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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