Accenture

Accenture

Posted via Workday

Deployment Lead

Posted Oct 27, 2026

Role at a glance

Salary
Not Disclosed
Location
Bengaluru
Work arrangement
On-site
Employment
Full-time
Experience
Minimum 7.5 year(s) of experience is required
Education
Educational Qualification : 15 years full time education

Spotted an issue?

We’ll check it against the original posting.

Log in to report

Role Summary

AI-generated

This posting, titled Deployment Lead, describes planning and leading the execution of a comprehensive deployment plan, including work planning, scheduling, budgeting, metrics, training, pilots, and resources, while managing interdependencies across project teams. Its summary centers on administering and supporting Veeva Vault RIM applications for global product registrations under GxP compliance. The position is based at the Bengaluru office BDC7.

What You'll Do

  • Serve as the primary Business Administrator and SME for the Veeva Vault RIM suite
  • Manage the full lifecycle of regulatory documents including authoring, review, approval, version control, metadata, and retention
  • Lead configuration, customization, and deployment of Veeva Vault RIM modules aligned with pharmaceutical quality standards
  • Manage Veeva release cycles and testing, including sandbox coordination, regression testing, and production deployments
  • Provide L1/L2 production support for Veeva Vault RIM applications per defined SLAs
  • Act as liaison between Regulatory Affairs, IT, Quality, and business stakeholders

Generated from the employer's posting. Verify important details before applying.

View full posting

Qualifications

Requires at least 7.5 years of experience with Veeva Vault skills, GxP and SDLC understanding, and 15 years of full-time education.

Required

  • Must have skill: Veeva Vault
  • Minimum 7.5 year(s) of experience is required
  • 15 years full time education
  • Minimum 3-5 years of experience in the pharma industry with a focus on regulatory affairs
  • Hands-on experience with Veeva Vault RIM Registrations and/or docuBridge supporting Global Regulatory Affairs and Safety functions
  • Strong understanding and experience of GxP processes and working in validated and regulated environments
  • Understanding of the SDLC process including change management, impact assessments, installation qualification, UAT testing, and...
  • Strong business analysis skills including the ability to elicit requirements and translate regulatory needs into practical solutions

Original job description

Content provided by the employer

Project Role : Deployment Lead
Project Role Description : Plan and lead the execution of a comprehensive deployment plan, including work planning, scheduling, budgeting, metrics, training, pilots, and resources. Collaborate with all project teams to manage interdependencies, ensure alignment between all deployment-related activities, and monitor & control progress through the deployment plan.
Must have skills : Veeva Vault
Good to have skills : NA
Minimum 7.5 year(s) of experience is required
Educational Qualification : 15 years full time education

Summary:
As a Veeva RIM Regulatory Registrations Business Administrator is responsible for managing, configuring, and supporting Veeva Vault Regulatory Information Management (RIM) applications with a primary focus on global product registrations. This role ensures seamless administration of the RIM suite, including Registrations, Submissions, Submissions Archive, and Publishing, while maintaining GxP compliance, data integrity, and regulatory alignment with FDA, EMA, ICH, and international Health Authority standards.

Roles & Responsibilities:
- RIM Suite Administration: Serve as the primary Business Administrator and SME for the Veeva Vault RIM
suite.
- Manage the full lifecycle of regulatory documents including authoring, review, approval, version
control, metadata, and retention. Manage IDMP data standards and structured data submissions.
- Configuration & Customization: Lead the configuration, customization, and deployment of Veeva Vault RIM
modules ensuring alignment with pharmaceutical quality standards and regulatory frameworks. Architect
workflows, object lifecycles, security models, and page layouts for scalable, compliant Vault
implementations.
- Release & Change Management: Manage Veeva release cycles and testing activities, including sandbox
coordination, regression testing, and production deployments. Analyze Veeva product releases for impact
and coordinate change control processes.
- Monitoring & Support: Monitor regulatory guidance and changes globally (FDA, EMA, ICH, local authorities). - Monitor system alerts and troubleshoot critical production issues. Provide L1/L2 production support for
Veeva Vault RIM applications per defined SLAs.
- Cross-Functional Collaboration: Act as liaison between Regulatory Affairs, IT, Quality, and business
stakeholders. Collaborate with other Veeva System Administrators to ensure continuity across workstreams. - Work with IT for integrations when data is shared cross-functionally.

Professional & Technical Skills:
- Must To Have Skills: Hands-on experience with Veeva Vault RIM Registrations and/or docuBridge supporting
Global Regulatory Affairs and Safety functions.
- Basic understanding of regional regulatory differences and how they can influence system requirements and
configuration-.
- Strong communication skills with the ability to communicate with both regulatory business stakeholders and
technical teams.
- Strong understanding and experience of GxP processes and working in validated and regulated
environments.
- Understanding of the SDLC process including change management, impact assessments, installation
qualification, UAT testing, and controlled deployment releases.
- Strong business analysis skills including the ability to elicit requirements, interpret regulatory needs, and
translate them into practical solutions.
- The candidate should have minimum 3–5 years of experience in the pharma industry with a focus on
regulatory affairs, including strong understanding of global regulatory processes and hands-on experience
with Veeva Vault RIM Registrations and/or docuBridge supporting Global Regulatory Affairs and Safety
functions.
- Strong communication skills and proactive engagement with multiple teams.

Additional Information:
- The candidate should have minimum 3–5 years of experience in the pharma industry
- The candidate should have 15 years of education.
- This position is based at our Bengaluru office BDC7.

15 years full time education

About Accenture

Accenture is a leading global professional services company that helps the world’s leading businesses, governments and other organizations build their digital core, optimize their operations, accelerate revenue growth and enhance citizen services—creating tangible value at speed and scale. We are a talent- and innovation-led company with approximately 791,000 people serving clients in more than 120 countries. Technology is at the core of change today, and we are one of the world’s leaders in helping drive that change, with strong ecosystem relationships. We combine our strength in technology and leadership in cloud, data and AI with unmatched industry experience, functional expertise and global delivery capability. Our broad range of services, solutions and assets across Strategy & Consulting, Technology, Operations, Industry X and Song, together with our culture of shared success and commitment to creating 360° value, enable us to help our clients reinvent and build trusted, lasting relationships. We measure our success by the 360° value we create for our clients, each other, our shareholders, partners and communities.

Visit us at www.accenture.com 

Equal Employment Opportunity Statement


We believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, military veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by applicable law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities.

Accenture

About the company

Accenture

Large Enterprise

Accenture is a global professional services company that specializes in providing consulting, technology, and outsourcing services. With a diverse range of industries served, including financial services, healthcare, and telecommunications, Accenture leverages advanced technologies and data analytics to help organizations improve their performance and drive innovation. Committed to sustainable progress, the company emphasizes its dedication to inclusivity, digital transformation, and building a more sustainable future for its clients and communities. With a presence in over 120 countries, Accenture is known for its expertise in integrating cutting-edge solutions that address complex business challenges.