{"schemaVersion":"jobsearcher.job.v1","id":"44ae4e2e3aaa0e3c583bf899","url":"https://jobsearcher.com/jobs/44ae4e2e3aaa0e3c583bf899","canonicalUrl":"https://jobsearcher.com/jobs/44ae4e2e3aaa0e3c583bf899","title":"Quality Operations Program Manager","description":"Overview\nIn this role you drive the integrity and compliance of Veeva’s Quality Management System across multiple product lines. You serve as the process owner for document control, shaping quality processes and records lifecycle. You provide regulatory interpretation and oversight for activities like process definition, validation testing, and releases. You build and monitor metrics to measure effectiveness of domain systems, enabling safer, compliant software in a fast-growing SaaS environment. This is a hands-on, cross-functional role at a mission-driven company focused on life sciences quality.\n\nCompensation / BenefitsMedical, dental, vision, and basic life insuranceFlexible PTO and company paid holidaysRetirement programs1% charitable giving programbasic life insurance\nResponsibilitiesOwn the Document Control process area and lifecycle management of quality recordsProvide quality oversight on regulated activities and deliverables (process definition, validation, releases/changes) for in-scope products and systemsOffer regulatory interpretation and guidance on federal regulations and quality system requirementsDevelop metrics and track effectiveness and productivity of domain systems\nKey requirements3+ years in a regulated quality role in Life SciencesExperience with Quality Management Systems (QMS) including document management, training, change control, CAPAExperience with electronic Document Management Systems (eDMS) and/or electronic Quality Management Systems (eQMS)Good understanding of GxP regulations (GMP, GCP, 21 CFR 11, ICH Q10, QSR) and quality frameworks (ISO 9001)Excellent process mapping, problem-solving, and communication skills to convey technical and regulatory conceptsprocess mappingproblem-solvingcommunicationVeeva Quality Cloud solutions (QualityDocs, QMS, Training)Quality Principles and Standards (ISO, IEC, IEEE, ITIL, ICH)Software development life cycle (SDLC)","company":"Veeva Systems","rawCompany":"veeva systems","city":"Quincy","state":"MA","isRemote":false,"isActive":false,"createdAt":"2026-09-15T04:24:52.984Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-9199.01","title":"Regulatory Affairs Managers","slug":"regulatory-affairs-managers"}],"industries":[{"code":"513210","title":"Software Publishers","slug":"software-publishers"},{"code":"541511","title":"Custom Computer Programming Services","slug":"custom-computer-programming-services"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Operations Program Manager","description":"Overview\nIn this role you drive the integrity and compliance of Veeva’s Quality Management System across multiple product lines. You serve as the process owner for document control, shaping quality processes and records lifecycle. You provide regulatory interpretation and oversight for activities like process definition, validation testing, and releases. You build and monitor metrics to measure effectiveness of domain systems, enabling safer, compliant software in a fast-growing SaaS environment. This is a hands-on, cross-functional role at a mission-driven company focused on life sciences quality.\n\nCompensation / BenefitsMedical, dental, vision, and basic life insuranceFlexible PTO and company paid holidaysRetirement programs1% charitable giving programbasic life insurance\nResponsibilitiesOwn the Document Control process area and lifecycle management of quality recordsProvide quality oversight on regulated activities and deliverables (process definition, validation, releases/changes) for in-scope products and systemsOffer regulatory interpretation and guidance on federal regulations and quality system requirementsDevelop metrics and track effectiveness and productivity of domain systems\nKey requirements3+ years in a regulated quality role in Life SciencesExperience with Quality Management Systems (QMS) including document management, training, change control, CAPAExperience with electronic Document Management Systems (eDMS) and/or electronic Quality Management Systems (eQMS)Good understanding of GxP regulations (GMP, GCP, 21 CFR 11, ICH Q10, QSR) and quality frameworks (ISO 9001)Excellent process mapping, problem-solving, and communication skills to convey technical and regulatory conceptsprocess mappingproblem-solvingcommunicationVeeva Quality Cloud solutions (QualityDocs, QMS, Training)Quality Principles and Standards (ISO, IEC, IEEE, ITIL, ICH)Software development life cycle (SDLC)","datePosted":"2026-09-15T04:24:52.984Z","dateModified":"2026-09-15T04:24:52.984Z","hiringOrganization":{"@type":"Organization","name":"Veeva Systems","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Quincy","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"44ae4e2e3aaa0e3c583bf899"},"url":"https://jobsearcher.com/jobs/44ae4e2e3aaa0e3c583bf899"}}