Spécialiste en validation et en tests de systèmes / System Validation and Testing Specialist
IQVIALaval (administrative region), Quebec, Canada
Posted March 4, 2026
Full Time
About the Company
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.
Job Description
The Validation Specialist provides expertise for the implementation, modification, and decommissioning of regulated laboratory equipment and computerized laboratory systems. The role ensures full compliance with internal procedures and industry best practices, evaluates project resources, analyzes user needs, and oversees the documentation, testing, and maintenance of laboratory equipment and computerized systems.
Requirements
- Lead multiple validation projects simultaneously
- Write, review, and approve validation deliverables
- Oversee the full lifecycle management of laboratory equipment and software
- Administer access to regulated systems and train laboratory personnel
- Provide expert support for laboratory equipment, computerized systems, and complex Excel spreadsheets
