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.
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
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
Other Equivalent combination of education, training, and experience may be accepted in lieu of degree
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
We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.
To learn more about our benefits, visit https://jobs.iqvia.com/benefits.
If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $51,800.00 - $108,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.