{"schemaVersion":"jobsearcher.job.v1","id":"063c2ea80bdee49192ba6f50","url":"https://jobsearcher.com/jobs/063c2ea80bdee49192ba6f50","canonicalUrl":"https://jobsearcher.com/jobs/063c2ea80bdee49192ba6f50","title":"CQV Sample Management / LIMS Coordinator","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\n\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\n\nCQV Sample Management / LIMS Coordinator\n\nJob Summary:\nWe are seeking an experienced CQV Sample Management / LIMS Coordinator to support cleaning characterization and sterilization execution activities in a GMP biologics manufacturing environment.\n\nThe individual will be responsible for coordinating sampling logistics, LIMS activities, labels, sample kits, laboratory interfaces, and results tracking to ensure samples and analytical results are available within required project timelines.\n\nPrepare and manage LIMS templates for project sampling activities.\nCoordinate sample labels, sample kits, containers, swabs, and other consumables.\nVerify availability of sampling supplies prior to manufacturing execution.\nCoordinate sample plans with CQV, Manufacturing, and QC Laboratories.\nSupport sample collection, custody, documentation, and delivery to QC.\nEnter and track samples within LIMS.\nMonitor laboratory results against established service-level expectations.\nMaintain sample status trackers and communicate pending or delayed results.\nSupport cleaning RFU and sterilization Conditional Release activities requiring analytical results.\nEnsure sampling documentation is complete, accurate, and GMP compliant.\nSupport TOC and microbial surface-sampling activities when qualified.\nCoordinate closely with CQV Technical Leads during 24/7 execution periods.\n\nRequired Qualifications\n\nExperience supporting sample management within a GMP pharmaceutical, biotechnology, or laboratory environment.\nExperience with LIMS or comparable laboratory-information systems.\nStrong organizational and documentation skills.\nKnowledge of GMP sample traceability and chain-of-custody requirements.\nAbility to coordinate multiple samples and priorities during active manufacturing campaigns.\n\nPreferred Qualifications\n\nCleaning validation or CQV experience.\nExperience with TOC and microbial sampling.\nPrevious experience with Amgen LIMS systems or manufacturing operations.\nFamiliarity with Kneat, PI, Smartsheet, LMS, MAXIMO, or similar applications.\n\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\n\nExcited to build something meaningful together? We look forward to hearing from you.\n\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","company":"Validation","rawCompany":"validation","city":"Juncos","state":"PR","isRemote":false,"isActive":false,"createdAt":"2026-09-04T11:46:24.516Z","occupations":[{"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"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"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":"CQV Sample Management / LIMS Coordinator","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\n\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\n\nCQV Sample Management / LIMS Coordinator\n\nJob Summary:\nWe are seeking an experienced CQV Sample Management / LIMS Coordinator to support cleaning characterization and sterilization execution activities in a GMP biologics manufacturing environment.\n\nThe individual will be responsible for coordinating sampling logistics, LIMS activities, labels, sample kits, laboratory interfaces, and results tracking to ensure samples and analytical results are available within required project timelines.\n\nPrepare and manage LIMS templates for project sampling activities.\nCoordinate sample labels, sample kits, containers, swabs, and other consumables.\nVerify availability of sampling supplies prior to manufacturing execution.\nCoordinate sample plans with CQV, Manufacturing, and QC Laboratories.\nSupport sample collection, custody, documentation, and delivery to QC.\nEnter and track samples within LIMS.\nMonitor laboratory results against established service-level expectations.\nMaintain sample status trackers and communicate pending or delayed results.\nSupport cleaning RFU and sterilization Conditional Release activities requiring analytical results.\nEnsure sampling documentation is complete, accurate, and GMP compliant.\nSupport TOC and microbial surface-sampling activities when qualified.\nCoordinate closely with CQV Technical Leads during 24/7 execution periods.\n\nRequired Qualifications\n\nExperience supporting sample management within a GMP pharmaceutical, biotechnology, or laboratory environment.\nExperience with LIMS or comparable laboratory-information systems.\nStrong organizational and documentation skills.\nKnowledge of GMP sample traceability and chain-of-custody requirements.\nAbility to coordinate multiple samples and priorities during active manufacturing campaigns.\n\nPreferred Qualifications\n\nCleaning validation or CQV experience.\nExperience with TOC and microbial sampling.\nPrevious experience with Amgen LIMS systems or manufacturing operations.\nFamiliarity with Kneat, PI, Smartsheet, LMS, MAXIMO, or similar applications.\n\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\n\nExcited to build something meaningful together? We look forward to hearing from you.\n\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","datePosted":"2026-09-04T11:46:24.516Z","dateModified":"2026-09-04T11:46:24.516Z","hiringOrganization":{"@type":"Organization","name":"Validation","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Juncos","addressRegion":"PR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"063c2ea80bdee49192ba6f50"},"url":"https://jobsearcher.com/jobs/063c2ea80bdee49192ba6f50"}}