Senior QA Manager, Quality Systems

• Drive and continuously improve the QMR process, including governance, data inputs, facilitation, documentation, follow-up, and effectiveness tracking
• Drive continued implementation of the process landscape, ensuring processes are well-defined, understood, and embedded with clear ownership and interfaces
• Own and enhance core QA processes (e.g., Change Control, Deviation management, P)) and implement continuous improvements
• Build and maintain quality reporting for QMR (e.g., KPIs, dashboards, and trend analyses) using Veeva Vault, Excel, and BI tools to enable timely, decision-ready oversight
• Present and represent QA processes, QMR outcomes, and key metrics during audits and inspections, ensuring transparent and consistent communication
• Collaborate with IT and key stakeholders to define and communicate requirements for our electronic QMS (Veeva Vault Quality) to support process execution and reporting

• Master's degree in a relevant field and 5+ years of QA experience, preferably within pharmaceutical development
• Solid understanding of pharmaceutical quality systems and quality process governance
• Demonstrated ability to analyze quality data and deliver clear reporting (e.g., KPIs, dashboards, trend analyses) to support decision-making
• Highly organized with the ability to translate structure into effective, sustainable process improvements
• Strong communicator and collaborative team player, with a pragmatic and compliant approach
• Experience working with electronic QMS/EDMS and reporting tools (e.g., Veeva Vault, Excel, BI) is an advantage

Experience working with electronic QMS/EDMS and reporting tools (e.g., Veeva Vault, Excel, BI)