If you are looking to advance your career in Regulatory Affairs, Pharmacovigilance systems, and RIM platforms, this opportunity at Elanco offers a strong platform to work on global regulatory data and system operations.
The Regulatory Information System Associate role focuses on managing regulatory data, ensuring compliance, and supporting global RAP (Regulatory Affairs & Pharmacovigilance) teams using Veeva Vault RIM. This is a high-impact role ideal for professionals with 2–5 years of regulatory affairs or data management experience.
📍 Location: Bangalore
🕒 Job Type: Full-time
Key Responsibilities
- Manage end-to-end regulatory activities including:
- Event creation
- Applications, submissions, and registrations
- Regulatory tracking and lifecycle management
- Maintain and update regulatory data in Veeva Vault RIM system
- Own and manage Document Request Process (DRP)
- Ensure data integrity, compliance, and system accuracy
- Act as a subject matter support for RIM system users
- Conduct training sessions and troubleshooting support
- Generate and communicate KPI metrics for RIM system performance
- Collaborate with RAP, R&D, and Manufacturing & Quality teams
- Stay updated with global regulatory guidelines
Qualifications & Skills
Mandatory Qualifications
- Degree: B.Pharm, M.Pharm, MSc, DVM, or Veterinary Sciences
- Experience: 2–5 years in:
- Regulatory Affairs
- Pharmacovigilance systems
- Data management
Core Skills
- Knowledge of global regulatory requirements
- Hands-on or working knowledge of Veeva Vault RIM
- Strong data handling & system management skills
- Excellent communication and stakeholder management
- High attention to detail and ability to manage multiple projects
Preferred Skills
- Experience in system audits
- Ability to work cross-functionally in global teams
Benefits of Working at Elanco
- Opportunity to work with a global leader in animal health
- Exposure to regulatory operations across multiple geographies
- Hands-on experience with Veeva Vault RIM (high-demand skill)
- Inclusive and diverse work culture
- Strong career growth in Regulatory Affairs & PV systems domain
Why This Role Matters
This position is critical in ensuring regulatory compliance, submission accuracy, and system efficiency across global markets. If you are targeting careers in:
- Regulatory Affairs (RA)
- Pharmacovigilance Systems
- Veeva Vault / RIM Platforms
- Global Submission Management
—this role provides strong domain exposure and scalability.
Application Instructions
