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Tier-1 brand, metro location, and mid-level experience increase competition but niche Veeva specialization limits applicant pool.
Strong Veeva Vault and life-sciences regulatory expertise required makes the role highly industry-specific and less transferable.
Mandatory 3+ years Veeva Vault experience plus CSV/regulatory requirements create strict technical and domain filters.
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Design, configure, and manage lifecycle of Pfizer’s Veeva RIM system across assigned domains including objects, workflows, security, and business rules.
Lead end-to-end delivery of Veeva Vault RIM configuration changes within a SAFe Agile team, including release planning, execution, risk management, and stakeholder communication.
Ensure compliance with computerized system validation (CSV) through governance, testing support, integration enablement, and technical guidance across teams.
Bachelor’s degree in computer science, Information Systems, Engineering, or related field.
2-5 years of relevant experience including 3+ years hands-on with Veeva Vault applications, preferably Vault RIM.
Strong understanding of Vault platform configuration, integrations (REST APIs, ETL, SSO), Agile delivery, and regulated environment controls (CSV).
Work Experience Required: 2-5 years relevant experience explicitly mentioned.
Experienced in regulatory business processes and Life Sciences industry practices related to RIM and Veeva Vault configurations.
Comfortable operating within SAFe Agile framework and collaborating with cross-functional teams including product management, quality, and enterprise architecture.
Able to balance standardization and stakeholder needs while delivering scalable and compliant Vault RIM solutions with strong technical troubleshooting skills.