Accenture hiring Veeva Vault RIM Specialist Job in Bengaluru for regulatory submissions and Veeva Vault document management roles.
Introduction
Professionals with experience in Veeva Vault and Regulatory Information Management (RIM) systems can explore an excellent career opportunity with Accenture. The company is currently hiring for the position of Specialist – Veeva Vault / Regulatory Information Management for its life sciences consulting operations in Bengaluru, Karnataka.
This role is suitable for candidates with expertise in regulatory documentation, Veeva Vault workflows, and regulatory submissions management. The selected candidate will support global pharmaceutical clients by managing regulatory documentation systems, maintaining data integrity, and ensuring compliance with regulatory submission requirements.
Working with Accenture’s life sciences and regulatory technology teams offers exposure to advanced digital platforms and global regulatory processes used by pharmaceutical companies worldwide. Accenture hiring Veeva Vault RIM Specialist Job
Company Overview
Accenture is a global professional services company specializing in consulting, technology services, and digital transformation solutions. The organization works with clients across various industries including healthcare, pharmaceuticals, biotechnology, and life sciences.
Within the life sciences sector, Accenture provides regulatory technology solutions that support pharmaceutical companies in managing regulatory submissions, compliance documentation, and digital regulatory transformation. By integrating technology platforms like Veeva Vault, the company helps organizations streamline regulatory operations and improve compliance efficiency.
With offices and teams operating worldwide, Accenture offers professionals opportunities to work on global projects while developing expertise in regulatory affairs and digital platforms. Accenture hiring Veeva Vault RIM Specialist Job
Job Overview
| Job Details | Information |
|---|---|
| Company Name | Accenture |
| Job Role | Specialist – Veeva Vault / Regulatory Information Management |
| Industry | Pharmaceutical / Life Sciences / Regulatory Affairs |
| Job Location | Bengaluru, Karnataka, India |
| Employment Type | Full-Time |
| Experience Required | 1 – 3 Years |
| Qualification | B.Pharm, M.Pharm, B.Sc, M.Sc, Pharm.D, Biotechnology, Life Sciences |
| Application Mode | Email Application |
| Preferred Joining | Immediate Joiners |
Job Location & Employment Type
The selected candidate will work from Bengaluru, Karnataka, one of the major technology and consulting hubs for Accenture’s life sciences operations.
This is a full-time position within regulatory technology and regulatory affairs support teams. The role involves managing regulatory information systems and supporting documentation workflows used in pharmaceutical regulatory submissions. Accenture hiring Veeva Vault RIM Specialist Job
Open Positions / Department Details
Position: Specialist – Veeva Vault / Regulatory Information Management
Department: Regulatory Affairs / Regulatory Technology
The Regulatory Information Management (RIM) team focuses on maintaining regulatory documentation systems, managing submission workflows, and ensuring compliance with global regulatory requirements.
Professionals in this department help pharmaceutical companies organize and maintain regulatory data required for drug approvals and regulatory communications. Accenture hiring Veeva Vault RIM Specialist Job
Key Roles & Responsibilities
Veeva Vault Document Lifecycle Management
The selected candidate will manage document lifecycle processes within the Veeva Vault platform, including document review, approval workflows, version control, and archival. Accenture hiring Veeva Vault RIM Specialist Job
Maintaining accurate and compliant documentation is critical for regulatory submissions and regulatory authority communications.
Regulatory Information Management Support
The role includes supporting Regulatory Information Management activities related to regulatory submissions, product registrations, and regulatory documentation tracking.
The candidate will assist regulatory teams in maintaining accurate records within the regulatory system.
Data Integrity and Metadata Management
Ensuring the accuracy and consistency of regulatory data is a key responsibility. The candidate will monitor metadata fields, document attributes, and regulatory records to maintain data integrity.
Workflow Coordination
The candidate will manage regulatory workflows within the Veeva Vault system. This includes coordinating with regulatory affairs teams to ensure documents move through the approval process efficiently.
Cross-Functional Collaboration
The role requires coordination with regulatory, quality, and project teams to ensure submission documentation is prepared correctly and within timelines.
Effective collaboration helps ensure smooth regulatory submission processes.
Regulatory Compliance Monitoring
The candidate will ensure that regulatory documentation and submission processes comply with global regulatory guidelines and internal standard operating procedures.
Troubleshooting System Issues
The specialist may assist in identifying and resolving issues related to Vault workflows, document configuration, or user access management.
Providing technical support helps maintain smooth operation of regulatory information systems.
Eligibility Criteria
Candidates interested in this opportunity should meet the following requirements.
Education
Applicants must possess a Bachelor’s or Master’s degree in one of the following fields:
- Pharmacy (B.Pharm / M.Pharm / Pharm.D)
- Life Sciences
- Biotechnology
- Chemistry or related scientific disciplines
Experience
- 1 to 3 years of experience working with Veeva Vault or Regulatory Information Management systems
- Experience in regulatory submissions, document management, or regulatory operations is preferred
Skills Required
Ideal candidates should possess the following skills:
- Strong understanding of Veeva Vault document management workflows
- Knowledge of regulatory submissions and regulatory documentation processes
- Familiarity with health authority submission requirements
- Understanding of Regulatory Information Management systems
- Strong attention to detail and documentation accuracy
- Ability to collaborate with cross-functional regulatory teams
- Good communication and problem-solving skills
Preferred Qualification
Candidates holding Veeva Vault certification or similar regulatory technology certifications may have an advantage during the selection process. Accenture hiring Veeva Vault RIM Specialist Job
Salary & Benefits
Based on industry benchmarks for similar roles in India, the estimated salary range is:
₹6,00,000 – ₹10,00,000 per year
Additional benefits may include:
- Exposure to global pharmaceutical regulatory operations
- Opportunities to work with advanced regulatory technology platforms
- Professional development and training opportunities
- Career growth in regulatory affairs and digital regulatory systems
- Collaborative work environment with international teams
Selection Process
The recruitment process may include the following stages:
- Resume Screening
- Technical Interview (Veeva Vault / RIM knowledge)
- HR Discussion
- Final Selection
Candidates shortlisted for the position will be contacted by the Accenture recruitment team. Accenture hiring Veeva Vault RIM Specialist Job
How to Apply
Interested candidates who meet the eligibility requirements can apply by sending their updated resume via email.
Email Application
Applicants should ensure that their resumes highlight:
- Experience working with Veeva Vault systems
- Knowledge of regulatory submissions and documentation workflows
- Experience in regulatory information management platforms
Candidates who are available for immediate joining and have prior Veeva Vault experience are strongly encouraged to apply. Accenture hiring Veeva Vault RIM Specialist Job
Important Dates
- Application Deadline: Not specified
Candidates are advised to apply as early as possible. Accenture hiring Veeva Vault RIM Specialist Job
Why Apply for This Pharma Job?
Regulatory Information Management and Veeva Vault roles are becoming increasingly important in the pharmaceutical industry as companies adopt digital regulatory systems to manage complex global submissions.
Working with Accenture provides professionals the opportunity to gain experience with regulatory technology platforms used by major pharmaceutical companies. This exposure helps candidates develop expertise in digital regulatory systems, regulatory documentation management, and global regulatory compliance.
Such experience can lead to career advancement in regulatory affairs, regulatory technology consulting, Veeva Vault administration, and global submission management roles. Accenture hiring Veeva Vault RIM Specialist Job
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform that shares pharmaceutical and healthcare industry job updates for informational purposes only.
We do not conduct recruitment or charge any fees for job applications. Candidates should verify job details directly with the official company or recruiter before applying. IndiaPharmaJobs.in is not affiliated with Accenture or any organization mentioned in the job posting. Accenture hiring Veeva Vault RIM Specialist Job
Final Call-to-Action
Candidates with experience in regulatory information management systems and Veeva Vault workflows should consider applying for this opportunity. Send your updated resume to the provided email address and highlight your regulatory documentation expertise, Veeva Vault experience, and regulatory submission knowledge to improve your chances of being shortlisted for the Specialist – Veeva Vault / RIM role at Accenture. Accenture hiring Veeva Vault RIM Specialist Job
