Veeva Systems seeks a Technical Consultant to design and implement scalable integrations between Veeva Vault and third-party systems using the Vault Java SDK and REST APIs. The role is client-facing, requires Java experience (3+ years), cloud/integration knowledge (including AWS serverless), and up to 10% travel. This is a remote, full-time permanent position based in Germany (Berlin).

Full-time permanent Technical Consultant role focused on designing and implementing scalable integrations for Veeva Vault using the Vault Java SDK, REST APIs, and cloud technologies (AWS/serverless). Requires 3+ years programming experience (Java or other OOP), a technical degree, and up to 10% travel.

Remote, full-time permanent Technical Consultant position based in the UK (London) focused on designing and implementing scalable integrations between Veeva Vault and enterprise systems. Requires 3+ years programming experience (Java or other OOP), experience with REST-based APIs and cloud architectures, and up to 10% travel.

Remote, full-time Senior Technical Architect on the Patient CRM team at Veeva. The role designs, documents and implements end-to-end integrations between Patient CRM and external systems (hubs, specialty pharmacies, data aggregators) using middleware, REST/SOAP APIs and secure batch processes. Responsibilities include leading technical discovery workshops, technical design and build activities, supporting pre-sales architecture reviews, mentoring junior consultants, and collaborating with Product and Strategy. Requires 7+ years of technical consulting or architecture experience, deep Life Sciences domain knowledge, and strong integration and data security skills. Veeva does not anticipate providing visa sponsorship for this position; travel for implementations may be up to 25%.

Veeva is hiring a Senior Consultant to lead MedTech RIM implementations globally, guiding Regulatory Affairs and Operations transformations and ensuring customer adoption. Requires 8+ years in systems implementation, GxP ownership, or software consulting and 4+ years in Regulatory Affairs/Operations within Medical Device or Diagnostics. Experience with Veeva RIM or similar RIM solutions and knowledge of FDA, EU MDR/IVDR, UDI, and technical documentation is required. Location listed as Philadelphia, PA; role advertised as Work Anywhere/remote eligible. Base salary range: $80,000–$200,000 USD per year.

Experienced consultant role to lead RIM implementation workstreams for Veeva’s MedTech customers globally. Responsibilities include analyzing customer processes, configuring systems, serving as primary customer liaison, developing adoption/enhancement roadmaps, and guiding best practices for regulatory data and document management. Requires 8+ years in systems implementation/GxP/software consulting and 4+ years in Regulatory Operations/Regulatory Affairs within Medical Device or Diagnostics; direct experience with Veeva RIM or similar solutions and strong knowledge of global regulatory requirements (FDA, EU MDR/IVDR, UDI). Role is based in Chicago (Work Anywhere policy) and the listed base salary range is $80,000–$200,000 per year.

Senior consultant role leading end-to-end RIM implementation workstreams for MedTech customers, analyzing business processes, configuring systems, and advising on adoption and regulatory best practices. Requires 8+ years in systems implementation or software consulting, 4+ years in regulatory operations/affairs for medical devices/IVDs, and direct experience with Veeva RIM or similar solutions. Base salary range listed: $80,000–$200,000.

Full-time permanent consultant role on Veeva's Professional Services team focusing on Regulatory Information Management (Veeva Registrations, Submissions, Submissions Archive, Publishing). Responsibilities include requirements gathering, solution design, configuration, deployment, and program/project management. Requires 3+ years' experience in life sciences or healthcare and ability to travel (25–50%).

The role partners with account teams to design and present demonstrations, workshops, and conference room pilots for Veeva Quality. Requires 5+ years in the Life Sciences Quality domain, hands-on experience with digital quality solutions (e.g., TrackWise, Documentum, MasterControl), 2+ years in software pre-sales or implementation, and professional working proficiency in English. Travel ~30-40%.

Veeva is hiring a remote Senior Consultant (Managed Services) to provide ongoing post-implementation support for QMS, Quality Docs, and Training (LMS) customers. Responsibilities include Vault configuration, process support (SOPs, CAPA, deviations, change control, audits), bulk data import/export, reporting, sandbox/production maintenance, and ad hoc customer training. Requires 8+ years in software configuration/support in life sciences, healthcare, or regulated industries; frequent customer interaction and periodic travel are expected.

Lead a multi-phased global implementation program for Veeva Quality Cloud, act as primary customer liaison, oversee release management and IT operations, and mentor project teams. Requires 8+ years' experience in IT project/program management or consulting, familiarity with SaaS and GxP, and willingness to travel 25–50%.

Senior consulting role in Veeva's Quality Practice focused on Consumer Products (including Food & Beverage and Chemicals). Responsible for leading large global projects, driving business development for $1M+ deals, mentoring teams, and advising C-suite customers on Quality, Manufacturing, and Supply Chain topics. Requires 10+ years of management consulting experience.

Individual-contributor Director role to lead Veeva's Regulatory product market strategy and act as the technical/commercial authority on Regulatory Information Management (RIM). Requires experience in regulatory submissions (eCTD/IDMP), regulatory operations consulting, and selling software/services to life sciences organizations; travel for customer meetings is required.

Join Veeva as a Solution Consultant to act as a trusted advisor between pharmacovigilance stakeholders and Veeva's Vault Safety platform. Responsibilities include analyzing customer PV challenges, configuring and delivering demonstrations, leading RFP/RFI responses, workshops and POCs, and collaborating with cross-functional teams. Role requires 5+ years in life sciences, deep PV process knowledge, presentation skills, and willingness to travel (20–30%).

Act as a trusted advisor and pre-sales solution consultant for Veeva's Vault Safety platform, analyzing pharmacovigilance challenges, delivering tailored demonstrations and RFP responses, leading workshops and proofs of concept, and supporting customer adoption. Requires 5+ years in life sciences, deep pharmacovigilance process knowledge, technical/SaaS familiarity, and fluency in German and English; travel ~20-30%.

Veeva seeks a Process Architect to lead digitalization of validation (CSV/CQV) processes by mapping legacy documents into structured Veeva Validation Management data, developing migration tooling, executing bulk data loads, and advising customers on best practices. Requires 5+ years in life sciences validation, experience in customer-facing consulting, and knowledge of industry standards such as ASTM E2500, ISPE Baseline Guides, and Annex 15.

Join Veeva to lead digitalization of commissioning, qualification, and validation processes by converting legacy documents into structured Vault environments. Responsibilities include extracting requirements from legacy Word documents, mapping to structured data/models, executing bulk data loads, developing migration tooling/methodologies, building libraries/templates, and advising customers on digital validation best practices. Requires 5+ years in life sciences validation (CSV/A and CQV), consulting or professional services experience, familiarity with ASTM E2500/ISPE/Annex 15, and ability to travel domestically and internationally (up to 30%).

Provide ongoing application administration and subject-matter expertise for Veeva Network customers, manage Network-to-CRM interfaces, recommend best-practice configurations (match/merge, survivorship, data model), perform configuration and data investigations (including SQL), triage and resolve issues, and advise on process and system optimization. Role requires 3+ years MDM or life sciences data operations experience and legal authorization to work in the United States.

Lead and participate in Veeva Align implementation projects for pharmaceutical and medical device clients, including business process due diligence, design, end-user requirements, advanced configuration, and documentation. Role includes project management, technical product work, executive stakeholder engagement, and mentoring team members. Requires 8+ years in technology consulting for commercial life sciences or pharma commercial operations, hands-on data management and process analysis skills (Excel, Access or SQL). Up to 20% travel; listed base salary range $80,000–$125,000.

Lead and deliver Veeva Align implementation projects for pharmaceutical and medical device customers, performing business process due diligence, requirements gathering, advanced configuration, and data/process analysis. Requires 8+ years in technology consulting or pharma commercial operations, hands-on data management skills (Excel, Access, SQL), and up to 20% travel.