TCS
1+Years
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TCS
RIM / REGULATORY OPERATIONS
Department: Regulatory Information Management (RIM)
Locations: Pune | Mumbai | Bangalore
Employment Type: Full-Time
ROLE
RIM / Regulatory Operations – xEVMPD / IDMP
EXPERIENCE
Minimum 1 year of relevant experience
QUALIFICATION
Bachelor’s / Master’s degree in Life Sciences, Pharmacy, or related fields
KEY RESPONSIBILITIES
* Manage regulatory information using Veeva RIM / Veeva Vault
* Process Data Entry Requests (DERs)
* Create and maintain Registration Objects (ROs) and Submission Objects (SOs)
* Perform regulatory data entry, validation, reconciliation, and quality checks
* Support regulatory reports, dashboards, and health-authority records
* Contribute to RIM process improvements, testing, validation, and UAT
* Manage xEVMPD data updates and submissions
* Support IDMP data management activities in line with applicable standards
REQUIRED SKILLS
* Knowledge of Regulatory Information Management
* Familiarity with Veeva RIM / Veeva Vault
* Understanding of xEVMPD and IDMP processes
* Strong data management and quality-checking skills
* Good analytical and documentation skills
* Ability to work effectively in a regulatory operations environment
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MailTo apply for this job email your details to raghulr190300@gmail.com