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Deployment Lead

Bengaluru, India Full-time
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Added 7 Nov 2026 · Other

Job description

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 Important Notice We have been alerted to the existence of fraudulent messages asking job seekers to set up payment to cover various costs associated with establishing employment at Accenture. No one is ever required to pay for employment at Accenture. If you are contacted by someone asking for payment, please do not respond, and contact us at india.fc.check@accenture.com immediately. Equal Employment Opportunity Statement All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law. Please read Accenture’s Recruiting and Hiring Statement for more information on how we process your data during the Recruiting and Hiring process.
Pay, skills & work eligibility

Compensation

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Location, eligibility & working hours

Listed work location
Bengaluru, India
Visa sponsorship
Not stated clearly
Relocation support
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Working hours / time zone
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Work authorization wording
All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by

Remote does not automatically mean work from any country. A location match does not confirm work authorization, sponsorship or relocation eligibility.

Requirements at a glance

Experience mentioned: 3–5 years

Communication

Named skills identified in the listing. A mention is not always a requirement; read the full description and employer conditions.

Location & work arrangement

Listed work locations

  • Bengaluru, India

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