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Strong employer brand and metro location but niche Veeva skill and seniority moderate.
Highly specialized Veeva Vault and regulatory expertise limits cross-industry transferability.
Explicit 7+ years, required Veeva Vault experience, CSV/regulatory expectations raise filtering stringency.
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Lead design, configuration, and lifecycle management of Pfizer’s Veeva RIM System across assigned domains ensuring alignment with global regulatory business processes.
Own end-to-end delivery of Veeva Vault RIM configuration changes including intake, build, test, deployment, and hypercare within a SAFe Agile team environment.
Ensure compliance with computerized system validation (CSV) standards through coordination with Quality and validation teams, and support integration, troubleshooting, and reporting across platforms.
Bachelor’s degree in Computer Science, Information Systems, Engineering, or related field.
7+ years relevant experience; 3+ years hands-on Veeva Vault application configuration and support (Vault RIM preferred).
Strong understanding of Vault platform capabilities and configuration including security, objects, lifecycles, rules, and environment management.
Experience with Agile delivery, SDLC controls, change management, release governance in regulated environments (CSV).
Experienced in configuring and supporting complex Veeva Vault RIM implementations with a focus on regulatory compliance in the Life Sciences domain.
Proven ability to deliver within a SAFe Agile framework, managing scope, risks, and stakeholder communications effectively.
Able to provide technical guidance and enable standardization and continuous improvement of Vault RIM configurations while balancing platform constraints and business needs.