About this role
This role at IQVIA provides global regulatory oversight for laboratory system validation management within the Quality Management System. It focuses on ensuring GxP-compliant validation governance across IQVIA Laboratories, including policy/procedure development and validation release oversight in a regulated clinical trial environment.
Required Skills
- Quality Assurance
- GxP Compliance
- Computer Systems Validation
- CSV Auditing
- SDLC
- CAPA
- Root Cause Analysis
- eQMS
- Risk Management
- Validation Documentation
+9 more
Qualifications
- Bachelor’s Degree
About IQVIA
iqvia.comIQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.
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