Role Description:
We are seeking a highly experienced and hands-on Veeva Technical Architect Veeva PromoMats to lead the architecture, design, implementation, integration, and optimization of enterprise-scale Veeva Vault PromoMats solutions for global Life Sciences organizations.
This role requires deep expertise in Veeva Vault PromoMats, strong enterprise architecture capabilities, regulatory understanding within pharmaceuticalbiotech environments, and the ability to lead complex digital content and medicallegalregulatory (MLR) review ecosystems. The ideal candidate will serve as the technical authority across business stakeholders, delivery teams, validation teams, and integration partners.
The candidate must be comfortable operating in a client-facing environment, driving technical strategy, governing best practices, and delivering scalable, compliant, and high-performing PromoMats solutions.
Required Qualifications
Bachelor s degree in Computer Science, Information Systems, Engineering, or related field.
15+ years of IT experience with at least 10+ years focused on Veeva Vault technologies.
7+ years of deep hands-on experience specifically with Veeva Vault PromoMats.
Strong expertise in:
Veeva Vault architecture
PromoMats implementation
Vault configuration and customization
DAM and MLR workflows
Vault APIs and SDK
Experience designing and implementing enterprise integrations.
Strong understanding of Life Sciences regulatory and compliance environments.
Experience with Agile and hybrid delivery methodologies.
Excellent communication, presentation, and stakeholder management skills.
Ability to work onsite with cross-functional business and technical teams in the US.
Preferred Qualifications
Veeva Vault certifications (highly preferred).
Experience with:
Veeva MedComms
Veeva CRM
Vault Quality
Vault RIM
Commercial content ecosystems
Experience with cloud platforms and middleware technologies.
Exposure to DevOps, CICD, automated deployment, and release governance for Vault environments.
Knowledge of AI-enabled content review or digital content operations is a plus.
Experience in large global pharmaceutical or biotech organizations.