{"schemaVersion":"jobsearcher.job.v1","id":"1ed18a9fe40bb9f8d16aa1fb","url":"https://jobsearcher.com/jobs/1ed18a9fe40bb9f8d16aa1fb","canonicalUrl":"https://jobsearcher.com/jobs/1ed18a9fe40bb9f8d16aa1fb","title":"CSV ENGINEER","description":"Hiring: CSV Consultant (Hybrid – CA)We are seeking an experienced Computer System Validation (CSV) Consultant to support a pharmaceutical client in CA. This is a hybrid role requiring onsite presence 3–4 days per week. The ideal candidate will have strong experience in Veeva platform validation, data migration, and end-to-end ownership of validation deliverables.Key Responsibilities:Execute and manage validation activities for Veeva Vault applications, including QMS, CTMS, RIM, and Quality DocsDevelop and execute User Acceptance Testing (UAT), including authoring detailed test scripts and test casesIndependently author, review, and manage validation lifecycle documentation such as URS, risk assessments, validation plans, protocols, and summary reportsCollaborate with cross-functional teams including Quality, IT, Regulatory, and Business stakeholders to ensure compliance and timely deliveryGather and document user and system requirements, translating business needs into User Requirements Specifications (URS)Manage Veeva Change Control processes, including initiation, assessment, implementation, and closureSupport and lead data migration activities, including defining migration strategy, identifying tools, ensuring data integrity, and preparing required documentationEnsure all validation activities comply with GxP, FDA, and industry regulatory standardsRequired Qualifications:Prior experience working as a CSV Consultant within the pharmaceutical or life sciences industryHands-on experience with Veeva Vault platform (QMS, CTMS, RIM, or Quality Docs)Strong understanding of the computer system validation lifecycle and regulatory requirements (GxP, 21 CFR Part 11)Experience in writing and executing validation documentation (URS, IQ/OQ/PQ, UAT)Proven experience supporting data migration projects and system implementationsAbility to work independently, manage multiple deliverables, and communicate effectively with stakeholdersWork Model: Hybrid role based in CA (3–4 days onsite per week)","company":"Shoolin","rawCompany":"shoolin","city":"California","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-05-28T12:39:08.726Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"15-1211.00","title":"Computer Systems Analysts","slug":"computer-systems-analysts"},{"code":"15-1299.08","title":"Computer Systems Engineers/Architects","slug":"computer-systems-engineers-architects"}],"industries":[{"code":"541512","title":"Computer Systems Design Services","slug":"computer-systems-design-services"},{"code":"541511","title":"Custom Computer Programming Services","slug":"custom-computer-programming-services"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"CSV ENGINEER","description":"Hiring: CSV Consultant (Hybrid – CA)We are seeking an experienced Computer System Validation (CSV) Consultant to support a pharmaceutical client in CA. This is a hybrid role requiring onsite presence 3–4 days per week. The ideal candidate will have strong experience in Veeva platform validation, data migration, and end-to-end ownership of validation deliverables.Key Responsibilities:Execute and manage validation activities for Veeva Vault applications, including QMS, CTMS, RIM, and Quality DocsDevelop and execute User Acceptance Testing (UAT), including authoring detailed test scripts and test casesIndependently author, review, and manage validation lifecycle documentation such as URS, risk assessments, validation plans, protocols, and summary reportsCollaborate with cross-functional teams including Quality, IT, Regulatory, and Business stakeholders to ensure compliance and timely deliveryGather and document user and system requirements, translating business needs into User Requirements Specifications (URS)Manage Veeva Change Control processes, including initiation, assessment, implementation, and closureSupport and lead data migration activities, including defining migration strategy, identifying tools, ensuring data integrity, and preparing required documentationEnsure all validation activities comply with GxP, FDA, and industry regulatory standardsRequired Qualifications:Prior experience working as a CSV Consultant within the pharmaceutical or life sciences industryHands-on experience with Veeva Vault platform (QMS, CTMS, RIM, or Quality Docs)Strong understanding of the computer system validation lifecycle and regulatory requirements (GxP, 21 CFR Part 11)Experience in writing and executing validation documentation (URS, IQ/OQ/PQ, UAT)Proven experience supporting data migration projects and system implementationsAbility to work independently, manage multiple deliverables, and communicate effectively with stakeholdersWork Model: Hybrid role based in CA (3–4 days onsite per week)","datePosted":"2026-05-28T12:39:08.726Z","dateModified":"2026-05-28T12:39:08.726Z","hiringOrganization":{"@type":"Organization","name":"Shoolin","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"California","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"1ed18a9fe40bb9f8d16aa1fb"},"url":"https://jobsearcher.com/jobs/1ed18a9fe40bb9f8d16aa1fb"}}