Scientist, Method Validation

IQVIAIthaca, NY
$51,800 - $108,000Onsite

About The Position

We are seeking Scientist, Method Validation (LC-MS) to join IQVIA Laboratories at Ithaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Scientist for Method Validation contributes to assay/method development by helping design and executing LC-MS validation experiments for small molecule assays. This role focuses on experimental testing and data interpretation to support method transfer and readiness for downstream sample analysis.

Requirements

  • Bachelor's degree in a relevant scientific discipline and 1 year of related experience in method or assay development or a specific methodology area
  • Working knowledge of LC-MS (LCMS) fundamentals, including data interpretation and recognizing data abnormalities
  • Understanding of sample handling and preparation and proficiency with relevant laboratory techniques
  • Ability to troubleshoot laboratory equipment and resolve process issues while knowing what to escalate versus address independently
  • Strong attention to detail, accuracy, and the ability to produce quality data and documentation to timelines
  • Effective communication and collaboration skills, including presenting results to support data review and transfer to Validation or Production labs
  • Good computer skills, including proficiency with Microsoft Excel, PowerPoint, and Word
  • Other Equivalent combination of education, training, and experience may be accepted in lieu of degree

Responsibilities

  • Execute assay validation experiments under moderate supervision in accordance with applicable SOPs
  • Operate LC-MS instrumentation for small molecule workflows, including set-up, runs, and basic instrument troubleshooting
  • Design and perform validation testing to assess assay robustness and support method transfer activities
  • Review, interpret, and summarize LC-MS data to determine whether results meet SOP requirements and inform next experimental steps
  • Support technical discussions, sponsor inquiries, and cross-functional collaboration with Validation and Method Development stakeholders
  • Assist with troubleshooting, process improvements, and escalation of complex assay or data issues to senior team members when appropriate
  • Prepare documentation including protocols, technical reports, summaries, quantitative analyses, and maintain compliant laboratory notebooks and good documentation practices

Benefits

  • Integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being
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