IN_Senior Associate_Veeva RIM Consultant_Enterprise Apps-SFDC_Advisory_Bangalore
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Job Description
Structured overview of role & requirementsAbout This Role
Configure and implement Veeva Vault RIM applications including Registrations, Submissions, Submissions Archive, and Publishing for global life sciences clients.
Collaborate with regulatory affairs teams to analyze business requirements, conduct workshops, prepare documentation, and support system testing, validation, and deployment.
Ensure compliance with GxP, FDA, EMA, and global regulatory standards, manage release activities, application enhancements, and production support.
Minimum Requirements
4 to 7 years total work experience with at least 2 to 3 years of hands-on Veeva Vault RIM implementation and configuration experience.
Bachelor's or Master's degree in Engineering, Pharmacy, Life Sciences, or related field is required.
Strong knowledge of regulatory affairs processes and submission management within life sciences domain.
Experience with Veeva Vault configuration of workflows, security, document lifecycle, and metadata; familiarity with SDLC, Agile methodologies, and validation processes.
Ideal Candidate Profile
Experienced in working with global regulatory teams and understanding complex life sciences regulatory environments.
Capable of translating regulatory business requirements into functional Veeva Vault RIM configurations, documentation, and training materials.
Comfortable collaborating with technical teams on integrations, data migration, and supporting post-production activities ensuring regulatory compliance.