14 of 14 Veeva Jobs in the South East

degree is preferred but not required 1520 years of experience working with regulatory organisations, R&D, or the life sciences industry Direct experience with Veeva Vault Regulatory systems Working knowledge of regulatory operations, submissions and publishing, and the technology that supports them Strong experience operating within GxP settings, including ...

preferred but not required 15-20 years of experience working with regulatory organisations, R&D, or the life sciences industry Direct experience with Veeva Vault Regulatory systems Working knowledge of regulatory operations, submissions and publishing, and the technology that supports them Strong experience operating within GxP settings, including system ...

advanced degree is preferred but not required15–20 years of experience working with regulatory organisations, R&D, or the life sciences industryDirect experience with Veeva Vault Regulatory systemsWorking knowledge of regulatory operations, submissions and publishing, and the technology that supports themStrong experience operating within GxP settings, including system validation ...

cosmetics. Experience working with Regulatory, Quality, R&D or Product teams. Knowledge of Regulatory Information Management (RIM), PLM or QMS systems. Experience with Veeva RegulatoryOne/Vault is desirable, but comparable regulatory systems experience will be considered. Strong requirements gathering, process mapping and stakeholder management skills. Agile experience, including ...

working with pharmaceutical development IT systems and business processes (ELN, LIMS, CDS, LES, Informatics, Instruments, HPC, Regulatory). Example technologies include Benchling, Scilligence, Empower, Veeva Systems. Experience in large technology selection processes able to lead technical decision making. Strong technical background ideally from a hands-on IT engineering background ...

Requirements Bachelor's degree (or equivalent) required Strong experience in Biopharma, analytics, strategic consulting, business, or related area Strong data domain expertise in CRM- VEEVA, Ex-factory Sales- SAP, In-Market Sales- IQVIA Good understanding of Reporting tools such as Microstrategy, Tableau or Power BI Awareness and willingness ...

related to the design, development, documentation, testing and implementation of clinical eCRF databases. Design of eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio is expected. In addition, the EDC Clinical Trial Designer will ensure that all relevant standard operating procedures, CRF Standards, process ...

regulatory platforms strategy and collaborates with senior leaders to ensure compliant, scalable technology across GRAS. The role requires deep experience in regulatory operations, Veeva Vault, and GxP environments, with a track record of delivering robust, audit-ready solutions. #J-18808-Ljbffr ...

Veeva Systems, Inc. is seeking an Application Security Architect to provide security guidance to product engineering and IT, design secure solutions, drive security best practices, and establish architecture standards. You will partner with security leads to grow the security program, mentor junior members, present to steering committees and engineering ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

roadmaps, present to steering committees and engineering teams, and promote security awareness company wide. What You'll Do Build strong relationships and effectively influence Veeva’s product and IT engineering Translate security risks to business impact Research, prioritize, coordinate, and communicate security solution recommendations Provide security architecture advice … testing, CTF competitions, CVE research and/or Bug Bounty recognition Experience in Web and Mobile (Android/iOS) based application/service assessment Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. As an equal opportunity ...