Lead Complaints Management implementation workstreams for MedTech customers, analyse business processes and requirements, design and configure Veeva Vault solutions, and guide post-implementation adoption. Requires 5+ years in Medical Device complaints management and knowledge of FDA, EU MDR/IVDR, ISO 13485/14971, CAPA, and related regulations. Remote role for candidates authorized to work in the EU or UK.

Join Veeva's Falcon MLR team as an MLR/PRC expert responsible for maximizing reviewer agreement across EU markets. Responsibilities include leading regulatory monitoring, operationalizing the reviewer-feedback loop, diagnosing agent flags, building processes for user queries, and automating recurring tasks with AI. Requires hands-on MLR/PRC review experience (pharma/biotech/agency), knowledge of European codes (EFPIA or national codes such as ABPI, ENLI, FSA, Farmindustria, LEEM), and experience with Vault PromoMats.

Join Veeva as a Solution Consultant for Quality to lead business-focused demonstrations and configuration of Vault Quality (QMS, document control, training, batch release, validation). Requires 3+ years working with quality assurance software in regulated industries (pharma/biotech/medtech), strong English communication, and willingness to travel ~20–30% in the EU. Total compensation listed: 65,000–110,000 EUR.

Veeva is hiring a Technical Curriculum Developer focused on agentic AI to design and build hands-on training, coding-intensive courses (Java/REST API fluency), and working AI agent demos. The role requires hands-on experience building/configuring AI agents (e.g., LangChain, Claude Agent SDK), instructional design for technical audiences, and at least 3 years creating technical training or enablement content.

Customer-facing role responsible for leading strategic discovery with European life sciences customers, converting process and market learning into product, services, implementation and field recommendations, and building reusable enablement. Requires 10+ years' experience in life sciences manufacturing, quality or related enterprise software/consulting, working knowledge of batch disposition and ERP (e.g., SAP), and the ability to travel within Europe and occasionally globally.

The role facilitates and manages GCP project implementation audits and ensures adherence to Veeva quality processes across regulated domains (e.g., GCP, HIPAA, CSV). Responsibilities include performing GxP/quality reviews, authoring audit records, incident/CAPA investigations, supplier assessments, and supporting process improvement. Requires a bachelor's degree or equivalent, and 3+ years in a Clinical QA role in life sciences.

The Clinical Compliance Operations Specialist ensures adherence to GCP and other regulated-domain processes across Veeva products and services. Responsibilities include performing GxP/quality reviews of project deliverables, documenting audit findings and remediation, authoring audit records, conducting supplier assessments, providing quality oversight on validation testing and releases, and participating in incident/CAPA investigations. Requires a bachelor’s degree or equivalent and 3+ years in a Clinical QA role in life sciences.

Join Veeva as a Product Support Engineer to provide global technical support for Veeva Vault and its integrations (including Salesforce/Veeva CRM). Responsibilities include diagnosing and resolving production issues, replicating defects in test environments, coordinating releases, documenting processes, and interfacing with development, QA, product management, and professional services. Role is full-time (Mon–Fri) with rotational evening on-call coverage. The posting notes the employer cannot sponsor F1 or H-1B visas.

Manage a Professional Services team focused on Veeva RIM implementation and customer success. Responsibilities include hiring, performance management, staffing and resource management, executing as Services Delivery Lead for engagements (non-billable), coaching the team, supporting pre-sales and escalations, and coordinating across Sales, Product and Services. Requires 5+ years software implementation experience and 3+ years people management. Position is remote (EU/UK-based) with travel up to 25%. Total compensation range listed: 70,000–120,000 EUR.

Lead a Professional Services team focused on implementing Veeva RIM, responsible for hiring, performance management, staffing, and delivery oversight. The role combines hands-on delivery (up to 25% customer-facing time), operational excellence in utilization and resource management, and cross-functional coordination to drive customer and employee success. Requires 5+ years of software implementation experience and 3+ years of people management.

Remote, full-time permanent consultant role (Boston, MA locality) requiring 3+ years in AI strategy or implementation consulting. Responsibilities include advising drug safety clients on AI adoption and governance, building validation/testing frameworks and monitoring dashboards (CSV/GxP compliance), leading implementations and training, and supporting customer success. Travel up to 50%; employer does not anticipate visa sponsorship.

Veeva seeks a Services Engagement Manager to own end-to-end engagement design and delivery for Professional Services, including RFx responses, proposals, and statements of work. The role is remote (North America), customer-facing, requires ~10–15% travel, and prefers experience in life sciences/healthcare, clinical operations, pharmacovigilance, or RIM. Minimum 3 years delivering software implementation/enhancement projects. Base pay listed $85,000–$170,000.

Veeva seeks a Services Engagement Manager to act as a trusted advisor for professional services engagements—defining engagement design, drafting RFx responses, proposals and Statements of Work, collaborating across sales and delivery teams, and driving a high-volume pipeline. Requires 3+ years delivering software implementation projects and experience with scoping/planning; life sciences or healthcare domain experience is preferred. Role is remote (based in North America) with ~10–15% travel.

Lead eCOA implementations including protocol review, design and configuration, creation and management of deliverables (timelines, KOM, URS, UAT), support data management activities, and provide technical guidance across projects. Requires 7+ years eCOA experience; travel ~5-10%. Base salary range listed: $80,000–$200,000 (USD/year).

Veeva is hiring a Product Expert to act as the bridge between development teams, internal stakeholders, and customers. Responsibilities include product evangelism, creating educational content and demos, synthesizing customer feedback, collaborating with Product Managers to shape the roadmap, and providing advanced product support. Requires 3+ years in a customer-facing technology role and hands-on experience with enterprise SaaS platforms (examples: Veeva Vault, Salesforce).

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.

Lead end-to-end implementations of Veeva Network MDM for pharmaceutical and biotech clients: perform data analysis, design MDM configurations and integrations (Vault CRM), drive technical architecture, manage project delivery, and mentor junior consultants. Requires 5+ years consulting experience and 3+ years hands-on MDM configuration experience. Role based in the U.S. (Boston, MA) with 20–30% 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%.

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.