Responsible for defining, monitoring, and maintaining document control and related QMS processes across multiple product lines and regulated domains. Provides regulatory and technical expertise (GxP, 21 CFR Part 11, ICH Q10), oversees validation testing and product changes, and tracks process effectiveness. Requires 3+ years in a regulated quality role in life sciences.

Responsible for owning document control and lifecycle management within the Quality Management System, providing quality oversight for regulated activities (validation, releases/changes), delivering regulatory interpretation, and tracking effectiveness metrics. Requires a BS/BA or equivalent, 3+ years in a regulated quality role in life sciences, and experience with QMS/eQMS/eDMS and GxP regulations. Location listed as Pleasanton, California; position supports Work Anywhere arrangements.

Lead and grow a customer-facing implementation team focused on delivering next-generation, AI-enabled commercial content and MLR solutions. Responsibilities include hiring, performance management, resource and utilization oversight, supporting pre-sales and escalations, and partnering cross-functionally; role requires 5+ years in software services, 2+ years people management, and up to 25% travel.

Senior consultant role implementing Veeva Network MDM (or similar MDM) for pharmaceutical and biotech clients. Responsibilities include data analysis and solution design (~50%), technical architecture and integrations (~30%), and project leadership and coaching (~20%). Requires 5+ years consulting experience, 3+ years hands-on MDM configuration experience, ability to travel 20–30%, and legal authorization to work in the United States. Base pay listed at $80,000–$200,000 (annual).

Lead end-to-end implementations of Veeva Network MDM (or similar MDM platforms) for pharmaceutical and biotech clients. Responsibilities include data analysis and solution design, high-level technical architecture and integrations (SQL, ETL, APIs, CSV/FTP), project leadership, stakeholder workshops, and mentoring junior consultants. Role requires 5+ years consulting experience and ability to travel ~20–30%.

The role delivers Veeva Commercial Cloud implementations (PromoMats/DAM, Vault Platform, Medical) across life sciences clients in Europe. Responsibilities include project management, solution architecture, business/functional analysis, stakeholder management, and leading delivery teams. Requires 5+ years in implementation roles, hands-on Veeva PromoMats/Vault or Salesforce experience, ability to travel (~20%), and fluent English; additional EU languages (French, German, Italian, Spanish) are desirable.

Join Veeva as a Senior Consultant on the European Professional Services team to lead implementations of Veeva PromoMats/DAM and Vault Platform for pharmaceutical, consumer health, or medical device clients. Responsibilities include project delivery (PM, solution architect, functional analyst/PO roles), business process design, stakeholder management, technical leadership and mentoring, and contributing to internal delivery improvements. Requires 5+ years' experience in technology implementation projects, hands-on experience with Veeva PromoMats/Vault or Salesforce.com, strong consulting and communication skills, and the ability to travel (~20%). Fluent English required. Total compensation listed: 90,000–150,000 EUR (annual, range).

Join Veeva as a Senior Consultant in European Professional Services to own delivery of PromoMats/Vault implementation projects (roles include Project Manager, Solution Architect, Business/Functional Analyst). Requires hands-on experience with Veeva PromoMats or Vault (or Salesforce.com), 5+ years in technology implementation projects, strong consulting and stakeholder-management skills, fluent English, and willingness to travel (~20%). Veeva does not handle visa.

Veeva seeks a Global Program Manager to own customer success and service delivery for large commercial life sciences customers, partnering with customer leadership, IT, Product, and Sales. The role requires 7+ years in large-scale program management within pharmaceutical commercial functions, up to 50% travel, and supports hybrid/remote work. Listed base salary range: $100,000–$200,000 USD per year.

Owner of customer success and service delivery for Veeva’s Commercial product line, coordinating customer-facing teams, Sales, Product, and Product Support to define deployment, governance, and transformation roadmaps and drive product adoption. Requires 7+ years in large-scale program management in pharmaceutical commercial functions (Sales, Medical Affairs, Marketing), consulting experience for enterprise pharma clients, and up to 50% travel.

Lead service delivery and customer success for a major commercial-life-sciences customer, partnering with customer leadership, IT, Product, and Sales to define deployment, governance, and transformation roadmaps. Requires 7+ years in large-scale program management in pharmaceutical commercial functions, consulting experience, and willingness to travel up to 50%.

Join Veeva's Ostro team to lead full-lifecycle software implementations from kickoff to go-live, coordinate cross-functional teams, configure no-code flow-builder applications, perform QA and prepare MLR/PRC annotations, develop SOPs and templates to scale operations, and mentor junior project managers. Role based in Boston (Work Anywhere/flexible) with a minimum of 4 years' relevant implementation experience.

Veeva is hiring an Implementation Project Manager to own complex software implementations from kickoff to go-live for the Ostro team. Responsibilities include project delivery, risk management, configuring client applications with a no-code flow builder, QA testing, and preparing MLR/PRC annotations; the role requires 2+ years managing multiple concurrent SaaS implementations and strong client/stakeholder communication.

Veeva is hiring a Project Manager for the Randomization & Trial Supply Management (RTSM) team to serve as primary client contact, review protocols and produce User Requirements Specifications, manage deliverables (timelines, KOM, communication manuals, randomization and clinical trial material lists), facilitate UAT and system setup, provide technical advice, and cover Tier 3 on-call support. Requires RTSM experience and 2+ years of project management experience within the clinical trial industry.

Lead end-to-end delivery on large-scale Life Sciences consulting engagements, manage senior client relationships, oversee teams of 4+ consultants and project budgets of $1M+. Requires 8+ years in Life Sciences consulting and expertise in go-to-market strategy, brand planning, product launch, omnichannel, and segmentation.

Lead end-to-end delivery on large, global commercial engagements in Life Sciences; build senior customer relationships and account strategy; manage teams of 4+ consultants and project budgets of $1M+; provide domain expertise in go-to-market, brand planning, product launch, omnichannel and segmentation. Requires 8+ years in Life Sciences consulting and a bachelor's degree; experience with Veeva products and SaaS-enabled consulting is a plus.

Veeva Business Consulting seeks an Engagement Manager to lead end-to-end delivery on large, global Life Sciences projects. Responsibilities include account leadership, leading teams of 4+ consultants across multiple projects, managing project budgets of $1M+, and contributing to practice-building. Requires 8+ years in Life Sciences consulting, expertise in go-to-market, brand planning, product launch, omnichannel strategy, and strong stakeholder and financial management skills.

Full-time, permanent Work-Anywhere role to lead and execute computer system validation activities (releases, hot fixes, revalidation) for Veeva quality products. Responsibilities include creating/updating CSV deliverables (IQ/OQ, VPP, VSR, trace matrices), performing risk assessments and impact analysis, coordinating cross-functional validation and change control, and ensuring compliance with regulations (e.g., 21CFR11, 21CFR820, Annex 11). Requires a bachelor's degree (or equivalent) and at least 3+ years in a CSV role. Listed base salary range: $85,000–$120,000 (USD/year).

Senior CSV Lead / Program Manager responsible for planning and executing validation for product releases, hot fixes, and periodic revalidation. Duties include creating and reviewing CSV deliverables (risk assessments, validation plans/protocols, IQ/OQ, validation summaries), ensuring regulatory compliance (e.g., 21 CFR, Annex 11, ICH Q10), collaborating with product/SQA/engineering teams, and tracking validation issues to closure. Requires at least 3 years of CSV experience and familiarity with enterprise application validation and Agile methodologies.

Full-time, work-anywhere role to plan and execute CSV deliverables (risk assessments, validation plans/protocols, IQ/OQ, validation summaries), collaborate with Product/SQA/Engineering, ensure regulatory compliance (21CFRs, Annex 11, ICH Q10), and track validation issues to closure. Requires a bachelor’s in engineering/science or equivalent and at least 3 years' CSV experience.