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Tier-1 brand and Bangalore mid-level role but niche Veeva skill reduces applicant density.
Role requires life sciences regulatory and Veeva Vault domain expertise, limiting cross-industry transferability.
Requires specific Veeva RIM hands-on experience, life sciences domain knowledge, and explicit years of experience.
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Own configuration and implementation of Veeva Vault RIM applications including Registrations, Submissions, Submissions Archive, and Publishing for global life sciences clients.
Collaborate with regulatory affairs teams to gather requirements, design functional specifications, and support system testing, validation, deployment, and post-production.
Ensure compliance with GxP, FDA, EMA, and global regulatory standards while supporting release management, issue resolution, and application enhancements.
4 to 7 years of IT/Consulting experience in the Life Sciences domain including 2 to 3 years hands-on with Veeva Vault RIM.
Bachelor's or Master’s degree in Engineering, Pharmacy, Life Sciences, or related field (BE/BTech mandatory).
Experience in Veeva Vault configuration covering workflows, security, document management, as well as familiarity with SDLC, Agile, and validation processes.
Experience working with global regulatory teams and understanding of Regulatory Affairs processes and submission management.
Experienced consultant comfortable working cross-functionally with regulatory and technical teams in global life sciences environments.
Strong analytical and stakeholder management skills to conduct workshops, document requirements, and drive digital transformation initiatives.
Technical proficiency with Veeva Vault RIM including configuration, integration (REST APIs), and data migration capabilities.