Job Description:
- Implement, configure, and support Veeva Vault RIM applications.
- Support regulatory submissions, product registrations, and regulatory lifecycle management.
- Gather business requirements and collaborate with Regulatory Affairs and IT teams.
- Manage regulatory data, workflows, system enhancements, and UAT.
- Ensure compliance with pharmaceutical regulatory processes and GxP requirements.
Required Skills:
- Hands-on experience with Veeva Vault RIM.
- Strong understanding of Regulatory Affairs and Regulatory Operations.
- Experience with Registrations, Submissions, and regulatory data management.
- Knowledge of eCTD, GxP, and global regulatory processes.
- Excellent analytical and communication skills.
- Experience: 5+ years in pharmaceutical regulatory systems or relevant Veeva RIM experience.
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