Responsible for end-to-end ownership of core operational processes for Veeva’s global Business Consulting practice, driving operational discipline, tracking key metrics, auditing workflows, and delivering data-driven insights. Requires a bachelor's or equivalent experience (example: 2+ years), familiarity with analytics/data-visualization tools (Excel, Tableau, Power BI, Salesforce), strong stakeholder management, and ability to work across global teams.

Join Veeva professional services to implement Veeva LIMS and eQMS solutions for regulated life sciences/pharma customers. Responsibilities include workshops, requirements gathering, process design, documenting user stories/functional specs, solution configuration, data migration, and driving customer success across engagements. Requires 5+ years as a Business/Functional Analyst with Veeva eQMS; remote role based in India with potential travel. Veeva does not provide visa sponsorship for this position.

Implement and configure Veeva LIMS and Vault Quality Suite (Vault QMS, Vault QualityDocs, Vault Training) including workflows, document types, security, fields, page layouts, reports and notifications. Participate in solution design, workshops, data migration, and systems integration; ensure customer success throughout engagements. Requires a Bachelor's in life science/computer science or related, strong communication and analytical skills, exposure to life sciences compliance/CSV, and ability to travel as needed. Remote role; must be authorized to work in India (no sponsorship).

Veeva seeks a Senior Product Manager (LIMS) to lead product definition and delivery for its LIMS solution used in regulated life sciences manufacturing. Responsibilities include designing features, authoring design specs, prioritizing roadmap items, and working with customers, engineering, QA, and commercial teams. Requires 5+ years of enterprise software product management experience and experience launching B2B solutions in regulated industries. Location: Canada (Toronto) or US/Canada in Eastern time zone (remote flexibility). Base pay listed: 100,000–200,000 CAD.

Lead product management for Veeva's LIMS within Quality applications: design features, author specifications, prioritize roadmap, and coordinate with customers, engineering, QA, sales, and professional services. Requires 5+ years in enterprise product management, experience with B2B/regulatory environments, strong technical skills and communication. Candidates located in the US or Canada in the Eastern time zone (or one hour offset).

The role leads discovery, design, and end-to-end implementation of Veeva Vault CRM Events Management using the Vault Platform and automation tools. Responsibilities include configuring solutions, data migration, validation, integrations (e.g., PromoMats, OpenData), compliance reporting, cross-functional alignment, and mentoring team members. Location is Toronto, Canada; travel up to 25–30% is required. Base salary range listed: CAD 100,000–150,000.

Responsible for identifying and growing sales opportunities within a set of 5-10 accounts, managing multiple complex sales cycles, building account plans and business cases, and delivering analytics on account progress. Requires 5+ years quota-carrying account management experience and 3+ years selling SaaS. Base salary range listed: $80,000–$300,000.

Lead discovery, design, and end-to-end implementations of Vault CRM Events Management for life sciences clients using prescriptive, packaged solutions and automation. Requires 6+ years delivering enterprise SaaS/cloud event-management implementations; involves data migration, integrations, validation, compliance reporting, cross-functional alignment, team mentorship, and travel up to 25–30%. Base salary range listed: $80,000–$200,000 (USD).

Lead discovery, design, and delivery of Vault CRM Events Management implementations for life sciences customers using prescriptive packages, automation, and Vault Platform capabilities. Role requires 6+ years delivering enterprise SaaS/event management implementations, domain knowledge of life sciences events (speaker programs, advisory boards, transparency reporting), willingness to travel ~25–30%, and provides mentorship and cross-functional alignment.

Lead discovery, design, and implementation of Vault CRM Events Management using the Vault Platform and prescriptive delivery practices. Deliver event lifecycle solutions (speaker programs, advisory boards, attendee reconciliation, PromoMats integration) with a focus on compliance, automation, and long-term customer success. Requires 2+ years of enterprise SaaS/event management implementation experience and willingness to travel ~25–30%.

Lead discovery and design sessions and execute Vault CRM Events Management implementations using prescribed best practices and automation. Responsibilities include configuring the Vault Platform, managing data migration and validation, integrating event lifecycle components (speaker management, budgets, PromoMats, attendee reconciliation), and collaborating cross-functionally to ensure operational excellence and customer adoption. Role requires 2+ years of enterprise SaaS/event management implementation experience and willingness to travel up to 25–30%.

The role delivers implementations of Vault CRM Events Management for life sciences event operations (speaker programs, advisory boards, transparency reporting). Requires 2+ years delivering enterprise SaaS/cloud event management implementations, strong technical aptitude with cloud platforms, workflow engines and data integration, and willingness to travel ~25–30%.

Lead implementations of Veeva’s MedTech Quality Management Complaints solution: analyse customer processes, translate requirements into solution design, configure Vault, manage stakeholders and drive post-implementation adoption. Requires 5+ years in medical device complaints management, familiarity with FDA and EU MDR/IVDR requirements, ISO 13485/14971, GxP/SaaS concepts, and experience in life sciences quality or manufacturing. Remote, full-time role based in the EU or UK; candidates must have legal authorization to work in the EU or UK.

Veeva seeks an Implementation Consultant to lead commercial Vault CRM implementation projects—configuring/customizing Vault CRM, leading client workshops, UAT and training, and advising on business process harmonization. Role is based in Milan (Italy) or other EU locations; requires 3+ years consulting experience, fluent English, ~20% travel, and offers total compensation of 45,000–80,000 EUR.

Deliver and configure Vault CRM implementations and migrations for life sciences clients, lead client workshops, UAT and training, and translate business requirements into scalable solution designs. Requires 3+ years consulting experience, fluent English, ~20% travel; total compensation range 55,000–90,000 EUR.

Remote senior consultant (EU/UK) responsible for leading implementations of Veeva's MedTech Complaints Management solution: analyzing customer processes, translating requirements into solution design, configuring the cloud solution (Vault), and guiding post-implementation adoption. Requires 5+ years Complaints Management experience for medical devices and knowledge of FDA, EU MDR/IVDR, ISO 13485/14971 and related regulations.

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.

Lead and manage a technical team (10+ consultants) on Randomization & Trial Supply Management (RTSM) projects. Responsibilities include technical design, coding, enforcing coding best practices and libraries, project management, hiring, and customer-facing support. Requirements include a bachelor’s degree or equivalent, 5+ years in technical design and coding/leadership, expertise in C#, ASP.NET, XML, HTML, CSS, JavaScript, and proficiency in MSSQL. Less than 10% travel; base salary range $100,000–$200,000.

Join Veeva's Falcon MLR team to own review quality across the US market, operationalize reviewer feedback, lead regulatory monitoring, investigate agent decisions, and build AI workflows. The role requires hands-on MLR/PRC review experience, knowledge of US FDA/OPDP and the PhRMA Code, Vault PromoMats experience, and residence in the US.

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.