Veeva Jobs

Refine Results
1 - 20 of 75 Jobs

VEEVA CRM consultant

AIBC Solutions

Raleigh, North Carolina, USA

Contract, Third Party

Veeva CRM consultant raleigh NC onsite

Senior Veeva QMS Support Analyst

I.T. Solutions

San Francisco, California, USA

Contract

Sr. Veeva QMS Support Analyst San Francisco, CA Type: Contract Length: 3 months, maybe extensions Job Summary: We are seeking a detail-oriented and technically skilled Veeva QMS Support Specialist to provide end-user support, configuration assistance, and continuous improvement for our Veeva Quality Management System (QMS). This role serves as a bridge between Quality, IT, and end users, ensuring smooth implementation and operation of Veeva QMS modules including Change COntrol, Deviations (QE)

Veeva CRM Technical Lead/Consultant

Radiansys, Inc.

Alameda, California, USA

Full-time

Veeva CRM Technical Lead/Consultant FTE (Preferred) / Contract Alameda, CA 94502 (Onsite) We are seeking an experienced Veeva CRM Technical Lead/Consultant with a strong background in Salesforce and Life Sciences domain to support and drive our Veeva CRM initiatives. The ideal candidate will bring hands-on expertise in Veeva CRM configuration, support and integration, and cross-functional collaboration, especially in commercial and medical business processes. Prior experience working with global

Veeva Integration Associate/Manager

SunTechPros, Inc.

Remote

Contract

Veeva Integration Associate/ManagerRemote role, (If they local to Raleigh, NC that's a plus)W2 Position Position Overview: The Veeva Integration Associate will support the integration and optimization of Veeva Vault, Veeva CRM, and other Veeva applications within our organization. This role involves working closely with cross-functional teams to understand business requirements and translating them into effective technical solutions. You will be responsible for configuring, editing, and maintain

Veeva Admin/ Tech Lead

Atika Tech

No location provided

Contract

Position: Veeva Admin/ Tech Lead Location: Remote (Canada) Type: 6 months Contract to Hire Required Skills: Veeva Platform/UCV certified (Admin/Associate Admin) 10 + years of experience in Information Technology. 4+ years of experience in Pharma domain implementing/configuring Veeva Vault Must have an experience on Veeva CTMS, TMF, Site connect and SSU. Experience in end-to-end Veeva implementations as a Technical Lead Hands-on expertise in configuring Veeva. Extensive experience on Mile

Veeva Promomats

TekShapers

Michigan, USA

Full-time, Part-time, Contract, Third Party

Employment type Contract Job Title Veeva Promomats Job Location Lake County, IL Duration 12 Months + Experience level Mandatory Skills Veeva Promomats Job Description Hands on experience in designing solutions for Veeva Vault. Configuration experience with Veeva Vault promomats Successfully delivered big releases of Veeva Promomats

Business Product Owner with Veeva Vault

Arnex Solutions LLC

US

Contract, Third Party

Business Product Owner with Veeva Vault background Job Description: Defining Product Vision: Establishing and maintaining a clear vision for the product, ensuring it aligns with business goals and customer needs Quality Systems: Knowledge of Quality Systems in Life sciences is required Managing Product Backlog: Prioritizing and maintaining the product backlog, ensuring that the most valuable features are developed first Stakeholder Collaboration: Working closely with stakeholders to gather requi

Product Manager / Product Owner with Veeva | Contract | Cambridge, MA

Alpha Business Solutions LLC

Cambridge, Massachusetts, USA

Contract

Our large R&D focused global pharmaceutical client is seeking to hire a Product Manager/ Product Owner with Veeva experience for a 6 months plus contract. Location: Cambridge, MA | Two days/week from office. Pharmaceuticals/ Life Sciences experience is a must. Experience working with Clinical products Strong knowledge of EDC (Electronic Data Capture) and Visualization Applications Help run day to day, work with stakeholders, understand product, work with business teamsPlease apply with your int

Veeva Vault developer/RIM

EDPSI

Lawrence Township, New Jersey, USA

Contract

Direct NJ Based Pharmaceutical industry client is looking for the Veeva Submission consultants Veeva RIM Veeva Vault - RIM, QualityDocs, QMS, MedComms ,eTMF - Configuration, Administration ,Migration, Data Remediation Regulatory Information Management (RIM) Veeva Vault Certified

Sr. Business Analyst (Veeva RIM Publishing)

Spotline

Remote

Contract, Third Party

Position: Business Analyst - Veeva RIM Publishing Implementation Location: Remote, EST hours Duration: 12+ Months (with possible extension) Job description: 8+ years of experience as a Business Analyst, client completed the selection process for the publishing tools and Veeva was selected. The ideal candidate should have functional knowledge of publishing in addition to implementation experience in Veeva Publishing.SME on Veeva RIM Publishing.Should have experience in documentation of new proces

Veeva Senior Support Engineer

Katalyst Healthcares and Lifesciences

Indianapolis, Indiana, USA

Full-time

Job Description: We are looking for candidate over 5 years of experience with Veeva Vault QMS, demonstrating a strong understanding of quality management processes and a proven track record in support roles, handling technical issues and user queries. Excellent communication and collaboration skills are essential, enabling effective work both independently and as part of a team. Additionally, knowledge of regulatory requirements in the healthcare industry is a plus. This role is perfect for som

Senior Technical Architect - Veeva Vault/Java

Veeva Systems

Columbus, Ohio, USA

Full-time

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company - we made history in 2021 by becoming a public benefit corporation

Salesforce Veeva Consultant (PromoMats)

IBM

New York, New York, USA

Full-time

Introduction Join IBM's Veeva Practice team as a Strategist & Business Analyst for Veeva PromoMats, where you will be a key leader in shaping and proposing innovative solutions leveraging the power of Veeva and IBM's Consulting AI and Asset based capabilities. You will work closely with clients to understand their unique challenges and develop compelling, tailored solutions that drive digital transformation within healthcare & life sciences organizations. Your role and responsibilities In this

Validation Engineer

Katalyst Healthcares and Lifesciences

Philadelphia, Pennsylvania, USA

Full-time

Job Summary The Validation Engineer is responsible for executing equipment and system validation activities within a regulated biopharmaceutical environment. This role involves implementing validation protocols, documenting results, and ensuring compliance with regulatory requirements. The position is based in West Philadelphia, Pennsylvania with a hybrid work arrangement. Responsibilities: Proficiency in Kaye AVS validation software. Experience with Valpro validation management systems. Compet

CSV LEAD CONSULTANT

Nityo Infotech Corporation

King of Prussia, Pennsylvania, USA

Contract, Third Party

Mandatory Skills: CSV, Compliance and Assurance services, LIFE-SCIENCES (GXP FDA CSV IQ/OQ/PQ), Veeva, Argus, Defect Tracking Tools JIRA Primary Skill: Computer System Validation, Computed system assurance, GAMP, GxP risk assessments, Change Management Secondary Skil: JIRA Veeva Argus Agile and Waterfall methodology 10+ years Experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems Perform review

Manufacturing Associate

Zachary Piper Solutions, LLC

Durham, North Carolina, USA

Full-time

Piper Companies is seeking a Manufacturing Associate for an on-site contract position in Durham, North Carolina (NC). The Manufacturing Associate you will be integral to our production team, ensuring the efficient operation of manufacturing equipment and adherence to quality standards. Responsibilities of the Manufacturing Associate include: Oversee and operate biopharmaceutical manufacturing equipment. Adhere to SOPs and GMP guidelines to uphold product quality standards. Gain cross-trainin

CSV CONSULTANT :: Remote

TESTINGXPERTS, INC. DBA DAMCOSOFT

New Jersey, USA

Contract, Third Party

Mandatory Skills CSV, Compliance and Assurance services, LIFE-SCIENCES (GXP FDA CSV IQ/OQ/PQ), Veeva, Argus, Defect Tracking Tools_JIRA Primary Skill- Computer System Validation, Computed system assurance, GAMP, GxP risk assessments, Change Management Secondary Skill- JIRA Veeva Argus Agile and Waterfall methodology Jo Description: Strong experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems P

Clinical Data Manager

Intone Networks Inc.

Remote or Boston, Massachusetts, USA

Contract, Third Party

Responsibilities: Support the planning, setup, and acquisition of external clinical data at the study level, assisting in managing study start-up, conduct, and closeout activities.Assist in creating external data transfer agreements, ensuring alignment with Takeda Standards and specifications to support data integration, analysis, and reporting..Develop and maintain working relationships with key stakeholders like Clinical Data Management, Clinical Data Engineering, Standards, and other Study Ex

Marketing Associate

Horizontal Talent

Alameda, California, USA

Contract

We are seeking a dynamic Marketing Associate to join our team and contribute to exciting marketing projects. This role offers the opportunity to work on innovative initiatives that support product launches and promotional activities. Responsibilities Execute marketing projects related to promotional materials and programs for both international and U.S. markets. Collaborate with cross-functional teams to develop and implement marketing plans that align with business objectives. Manage the submis

Pharma Global Regulatory Affairs IT Solution Architect

Pozent

No location provided

Contract

Responsibilities: Architect and design IT solutions tailored to global Regulatory Affairs functions, including submissions, registration tracking, labeling, and IDMP compliance. Collaborate with business stakeholders to understand requirements and translate them into scalable, compliant, and efficient technology solutions. Lead end-to-end architectural governance for regulatory systems, including integrations with RIM, DMS, and Health Authority gateways. Design and optimize Cloud-native data pip