JD FORMAT Copilot said: Job Title: Regulatory Information Management (RIM) Associate Experience: 1+ Year Location: Open Qualification: B.Pharma, M.Pharma, Nursing, Life Sciences, Microbiology, Biochemistry, Zoology, Statistics, or related fields.

We are looking for a Regulatory Information Management (RIM) Associate with hands-on experience in Veeva RIM/RegVault and regulatory data management activities.

Mandatory

Skills - Veeva RIM / RegVault

- Regulatory Information Management (RIM)
- Data Entry Requests (DER)
- Registration Objects (RO)
- Submission Objects (SO)
- xEVMPD
- IDMP
- Regulatory Data Management Roles & Responsibilities - Process Data Entry Requests (DERs) in Veeva RIM.
- Create and maintain Registration Objects (ROs) and Submission Objects (SOs).
- Perform regulatory data entry, validation, and reconciliation activities.
- Manage submission records and health authority correspondence.
- Support regulatory reporting, audits, and inspection readiness.
- Maintain xEVMPD and IDMP data in compliance with regulatory requirements.t

📌 RIMS Associate (Bengaluru)
🏢 Tata Consultancy Services
📍 Bengaluru