Associate Director, Quality Risk Specialist
KI-Beschreibung
In this role, you will focus on developing quality narratives and embedding Quality by Design principles in clinical trials. You will partner with teams to manage risks, ensure compliance, and drive quality initiatives, all while adapting strategies to meet evolving challenges.
Anforderungen
8 Jahre- •Minimum 8+ years QA experience or relevant experience in quality management, biomedical science, clinical development, or regulatory compliance
- •B.S. or M.S. in Chemistry, Biology, Health, Quality related field, or equivalent
- •Demonstrated applied knowledge of ICH
/ GCP, regulatory guidelines, clinical research processes, and Quality Assurance principles