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.
What You'll Do
- 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.
Requirements
- 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%
Nice to Have
- 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
Perks & Benefits
- Work Remotely
- Flexible PTO
- Health and wellness programs
Comopensation
- Total compensation: 75,000 - 140,000 EUR
- The total compensation range listed here has been provided to comply with local regulations and represents a potential total compensation range for this role. Please note that actual total compensation may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position's total compensation may be composed of other types of compensation, such as variable bonus and/or stock bonus.
Skills Required
- 5+ years of experience in life sciences validation
- Deep technical understanding of CSV/A and CQV lifecycles
- Proven experience in a customer-facing consulting role
- Strong working knowledge of risk-based qualification approaches
- Bachelor's degree in Engineering (Chemical, Mechanical, Bioengineering, Electrical, or related technical field)
Veeva Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Veeva and has not been reviewed or approved by Veeva.
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Healthcare Strength — Health, dental, vision, life, disability, and mental health coverage are provided, alongside FSAs, wellness programs, and fitness stipends. These offerings present a comprehensive healthcare package relative to typical tech benefits.
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Equity Value & Accessibility — Equity is a meaningful component of total compensation, with RSUs/options cited as part of packages. Engineering examples highlight strong base pay paired with "good RSU + ISO."
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Wellbeing & Lifestyle Benefits — Work Anywhere flexibility, home‑office stipends, wellness programs, fitness reimbursements, and company‑sponsored events support day‑to‑day wellbeing. A 1% charitable giving allowance further enhances lifestyle and purpose-driven engagement.
Veeva Insights
What We Do
Veeva is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,000 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves.
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