Rubi Singh

Background

About Rubi Singh

Currently I am leading TRD Audit Management at Novartis, overseeing the end-to-end Audit process for both prequalification and qualification audits. I specialize in: 1. Handling of Audit CAPA, Deviations and Investigations. Preparation of annual audit plans 3. Updating of the information on SharePoint/ trackers, review the applicable documents for correctness and archival of necessary documents on SharePoint. Providing Administrative support in preparation of Quality Management Review meeting slide deck & metrics reporting. · 5. Preparation, approval, and management of QAAs. Developing and maintaining process SOPs, working procedures and process maps. · 7. Providing support for GMP External Audits and inspection management activities (HA and Self Inspection Audits). Maintaining Approved supplier list for GxP vendors. Preparation of UQAP (Unified Quality Audit Program), Audit preparation support and QARP (Quality assurance responsible Person) Role for audit CAPA management. What makes this role rewarding is the 360° exposure it provides — balancing insights from multiple stakeholders while contributing to operational excellence and regulatory alignment. I am passionate about building a career at the intersection of quality, strategy, and innovation, leveraging cross-functional collaboration to drive impact, enhance compliance, and continuously grow in the global pharmaceutical landscape.