Description
The role leads the implementation and integration of GMP quality control systems, including configuration, data migration, deployment, stakeholder engagement, project execution, risk and quality monitoring, and go-live support. It also supports CSV/CSA and IQ/OQ/PQ validation activities, regulatory compliance, system acceptance, and release readiness. The position requires at least eight years of experience in pharmaceutical, biotechnology, or regulated GMP environments, along with expertise in QC/Laboratory systems, validation, GAMP5, GxP, data migration, and cross-functional project delivery.
