2 of 2 Veeva Jobs in the South East

for a systems-minded quality professional to join our Global Development Quality Technology & Compliance (GDQTC) team. As Manager, GDQTC, you'll play a pivotal role in supporting QMOD-our Veeva Vault-based electronic Quality Management System (eQMS)-helping ensure it continues to meet the needs of our global clinical, regulatory, and quality functions. Whether coordinating improvements, resolving user queries … integrity and usability Leading or supporting process improvements tied to system performance and user experience This Role May Be For You: You're experienced with electronic quality systems (preferably Veeva Vault) and thrive on solving complex process challenges You enjoy being a connector-working cross-functionally and translating user needs into technical requirements You bring a keen eye for … Development, or supervised IT support are all highly relevant. Familiarity with Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), and the software development lifecycle for validated systems is required. Veeva Vault experience is strongly preferred. Experience generating quality reports, handling upgrades, or serving as a subject matter expert for regulated systems is a plus. Does this sound like you More ❯

managing system user accounts. Generate managerial KPI reports and escalate issues related to data quality performance and system functionality. Manage document uploads and imports into electronic document management system (Veeva Vault), including study reports and regulatory documentation. Execute quality assurance checks and cleanup activities on imported documents, ensuring data accuracy and proper attribute properties for regulatory submissions. Propose and … implement data quality improvements based on industry best practices and identified needs. Essential: BSc or MSc in a scientific discipline. Comprehensive knowledge of document management systems (e.g., Veeva Vault) Knowledge on IT systems and data management, familiar with the concept of databases. Critical Experience Experience in data and document management in Regulatory Affairs, within the agricultural or pharmaceutical industry. More ❯