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Overview Role Overview Responsible for Computer System Validation activities within a pharmaceutical manufacturing environment. Responsible for the development and execution of key validation and quality documentation including Qualification Plans, Test Plans, Requirements Traceability Matrices (RTMs), and Validation
The QRM lead is responsible for redefining and embedding a risk-based quality management approach for a new, digitally enabled biologics manufacturing facility. The role ensures that quality risk management is systematically applied across processes, systems, and operations,
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