{"schemaVersion":"jobsearcher.job.v1","id":"11098a30d3f51f1a8a243c57","url":"https://jobsearcher.com/jobs/11098a30d3f51f1a8a243c57","canonicalUrl":"https://jobsearcher.com/jobs/11098a30d3f51f1a8a243c57","title":"QA Specialist (Fully Remote)","description":"Location: Fully Remote\nEmployment Type: Full-Time\nDate Posted: 25/Aug/2026\nA leading global Pharmaceutical organisation is currently seeking an experienced QA Specialist to support a large portfolio of global validation projects.\n\nThis is a fully remote position, with working hours aligned to a USA time zone.\n\nRole Overview\n\nThe QA Specialist will provide quality oversight across validation activities, ensuring compliance with GxP regulations, data integrity requirements, and internal quality standards.\n\nWhile the primary focus is on QA validation and governance, experience in Computer System Validation (CSV) would be a strong advantage. The role centres on documentation review, risk-based quality oversight, and ensuring robust lifecycle compliance across systems and processes.\n\nKey Responsibilities\n\nProvide QA oversight of validation activities across global projects, ensuring compliance with GxP and internal quality standards\nReview and approve key validation deliverables, including:\nValidation Plans & Reports\nRequirements & Traceability Matrices\nTest Plans, UAT documentation, and test results\nData migration and system lifecycle documentation\nEnsure compliance with data integrity principles, 21 CFR Part 11, and Annex 11 requirements\nProvide risk-based QA oversight across the validation lifecycle\nSupport change control, deviation management, and CAPA processes\nIdentify and manage GxP risks across validation and system activities\nSupport audit and inspection readiness, ensuring documentation is audit-ready\nProvide guidance to cross-functional teams on QA processes, validation standards, and data integrity expectations\nCollaborate with validation and IT teams, with exposure to CSV activities where applicable\n\nRequirements\n\nDegree in a scientific, engineering, or related discipline\n5+ years’ experience in QA validation within a GxP-regulated pharmaceutical environment\nStrong experience in validation lifecycle documentation review and approval\nSolid understanding of GxP, data integrity, and regulatory requirements\nKnowledge of 21 CFR Part 11 and Annex 11\nExperience supporting global or complex validation projects\nStrong stakeholder engagement and communication skills\n\nNice to Have\n\nExperience with Computer System Validation (CSV) (QA oversight or hands-on)\nExposure to systems such as SAP, LIMS, or ELN\nExperience in API, biologics, or OSD manufacturing environments\nPrevious experience providing QA oversight on CSV or IT validation activities","company":"Dps Group","rawCompany":"dps group","isRemote":true,"isActive":false,"createdAt":"2026-08-28T10:18:27.807Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541990","title":"All Other Professional, Scientific, and Technical Services","slug":"all-other-professional-scientific-and-technical-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"QA Specialist (Fully Remote)","description":"Location: Fully Remote\nEmployment Type: Full-Time\nDate Posted: 25/Aug/2026\nA leading global Pharmaceutical organisation is currently seeking an experienced QA Specialist to support a large portfolio of global validation projects.\n\nThis is a fully remote position, with working hours aligned to a USA time zone.\n\nRole Overview\n\nThe QA Specialist will provide quality oversight across validation activities, ensuring compliance with GxP regulations, data integrity requirements, and internal quality standards.\n\nWhile the primary focus is on QA validation and governance, experience in Computer System Validation (CSV) would be a strong advantage. The role centres on documentation review, risk-based quality oversight, and ensuring robust lifecycle compliance across systems and processes.\n\nKey Responsibilities\n\nProvide QA oversight of validation activities across global projects, ensuring compliance with GxP and internal quality standards\nReview and approve key validation deliverables, including:\nValidation Plans & Reports\nRequirements & Traceability Matrices\nTest Plans, UAT documentation, and test results\nData migration and system lifecycle documentation\nEnsure compliance with data integrity principles, 21 CFR Part 11, and Annex 11 requirements\nProvide risk-based QA oversight across the validation lifecycle\nSupport change control, deviation management, and CAPA processes\nIdentify and manage GxP risks across validation and system activities\nSupport audit and inspection readiness, ensuring documentation is audit-ready\nProvide guidance to cross-functional teams on QA processes, validation standards, and data integrity expectations\nCollaborate with validation and IT teams, with exposure to CSV activities where applicable\n\nRequirements\n\nDegree in a scientific, engineering, or related discipline\n5+ years’ experience in QA validation within a GxP-regulated pharmaceutical environment\nStrong experience in validation lifecycle documentation review and approval\nSolid understanding of GxP, data integrity, and regulatory requirements\nKnowledge of 21 CFR Part 11 and Annex 11\nExperience supporting global or complex validation projects\nStrong stakeholder engagement and communication skills\n\nNice to Have\n\nExperience with Computer System Validation (CSV) (QA oversight or hands-on)\nExposure to systems such as SAP, LIMS, or ELN\nExperience in API, biologics, or OSD manufacturing environments\nPrevious experience providing QA oversight on CSV or IT validation activities","datePosted":"2026-08-28T10:18:27.807Z","dateModified":"2026-08-28T10:18:27.807Z","hiringOrganization":{"@type":"Organization","name":"Dps Group","sameAs":"https://jobsearcher.com"},"jobLocationType":"TELECOMMUTE","applicantLocationRequirements":{"@type":"Country","name":"US"},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"11098a30d3f51f1a8a243c57"},"url":"https://jobsearcher.com/jobs/11098a30d3f51f1a8a243c57"}}