Role Overview

We are looking for an experienced

Veeva RIM Specialist with strong functional and hands-on configuration expertise, particularly in

Submission Content Plans

. The ideal candidate should be capable of independently managing Veeva RIM configurations, change management, and regulatory submission-related requirements.

Key Responsibilities

- Configure and maintain Veeva RIM functionalities based on business requirements.

- Demonstrate strong functional expertise in Submission Content Plans.

- Independently manage configurations, including:

- Lifecycles

- Atomic Security

- Entry Criteria

- Action Triggers

- Own and execute change management activities, including configuration changes and enhancements.

- Work with business and regulatory stakeholders to understand submission workflows and configuration requirements.

- Support regulatory content management and submission processes.





- Ensure configuration changes are implemented effectively and aligned with business requirements.

Mandatory Skills & Experience

- 5+ Years of Experience.

- Strong hands-on experience with Veeva RIM.

- Excellent functional knowledge of Submission Content Plans.

- Proven experience in independent Veeva RIM configuration.

- Hands-on expertise in Lifecycles, Atomic Security, Entry Criteria, and Action Triggers.

- Ability to independently own and manage change management activities.

- Good understanding of regulatory submission processes.

Domain Knowledge

- Basic understanding of MedTech regulatory submission formats:

- PMA (Premarket Approval)

- 510(k) Submissions

- EU MDR Technical Documentation

- Candidates with a robust pharmaceutical regulatory background are also welcome, provided they have a basic understanding of MedTech submission requirements.

📌 Veeva RIM Specialist (India)
🏢 vueverse.
📍 India