Veeva RIM Specialist

vueverse.; India; On-site; INR 900,000 - 1,400,000; Full time

Job summary

vueverse. in India is seeking an experienced Veeva RIM Specialist with strong hands-on configuration expertise, especially in Submission Content Plans. The candidate will independently manage Veeva RIM configurations, change management, and regulatory submission requirements.

You will configure and maintain Veeva RIM functionalities, work with regulatory stakeholders, support submission processes, and ensure changes align with business needs.

Qualifications

• 5+ years of experience in Veeva RIM
• 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

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, and 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

Skills

Veeva RIM

Submission Content Plans

Configuration Management

Regulatory submission

Job description

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 strong pharmaceutical regulatory background are also welcome, provided they have a basic understanding of MedTech submission requirements.