Join Veeva as we lead the life sciences industry’s fundamental shift from digital documents to process digitalization. As Process Architect, you will be the hands-on architect of this transition, converting legacy, document-centric processes into a modern, data-centric ecosystem within Veeva Validation Management.
We are seeking a technical lead to convert legacy documents into normalized, relational data environments. This individual understands the requirements for mapping Commissioning, Qualification, and Validation processes, turning templates and static records into fluid, searchable, and actionable information.
In this role, you will act as a digitalization expert, guiding customers from paper-heavy or paper-on-glass solutions to data-centric workflows. You will also be responsible for owning the development and maintenance of specialized tooling and methodologies required to migrate and manage data across Vault environments.
This is a work anywhere, full-time permanent role with Veeva. Our work processes are designed so that you can be productive in the environment that works best for you. This is a customer-facing role and we have no work location requirement if you are in close proximity to an airport and able to meet future travel requirements.
Collaborate with customers to extract requirements from legacy Word documents and map them into structured Vault environments
Reconcile customer-specific metadata to ensure data alignment and consistency across the entire validation lifecycle
Execute bulk data loads and manage staged data for customer workshops and process exercises
Partner with customers as a trusted advisor on best practices for importing and utilizing Validation Management for digitalized workflows
Build and maintain libraries of digital records and examples to support customer implementations of application templates
Develop and own the specialized tooling and methodologies required to migrate and manage relevant data across Vault environments
Execute billable project work across various service tiers ranging from artifact mapping to enterprise-level deployments
Partner with the strategy, services, and business consulting organizations to ensure an exceptional customer experience that reflects a deep understanding of validation processes across computer systems, equipment, cleaning, etc.
5+ years of experience in life sciences validation with a deep technical understanding of CSV/A and CQV lifecycles for facilities, utilities, and manufacturing equipment
Proven experience in a customer-facing consulting or billable professional services role with the ability to lead technical workshops and advise executive stakeholders
Experience mapping complex customer business processes into standardized data languages to move organizations to paperless validation models
Strong working knowledge of risk-based qualification approaches and industry standards such as ASTM E2500, ISPE Baseline Guides, and Annex 15
Proficiency in bulk data loading tools and managing data integrity within cloud-based platforms
Strong analytical skills for identifying configuration gaps between legacy customer data and system templates
Bachelor’s degree in Engineering (Chemical, Mechanical, Bioengineering, Electrical, or related technical field)
Ability to travel domestically and internationally for key customer engagements and internal meetings up to 30% with typical travel around 15%
Active participation or leadership within ISPE, EMA, or other industry technical committees or networks
Direct experience leading large-scale, enterprise digital validation implementations and rollouts
Previous experience in organizational change management within a manufacturing or quality environment
Familiarity with data transfer methodologies or specialized migration tooling
Work Remotely
Flexible PTO
Health and wellness programs
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