{"schemaVersion":"jobsearcher.job.v1","id":"68eecf94e1be6d8ecf266432","url":"https://jobsearcher.com/jobs/68eecf94e1be6d8ecf266432","canonicalUrl":"https://jobsearcher.com/jobs/68eecf94e1be6d8ecf266432","title":"CQV Engineer - Commissioning, Qualification & Validation","description":"Employment Type: Contract\n\nDuration: 9 Months\n\nStatus: Accepting Candidates\n\nAbout the Role\nWe are seeking an experienced CQV Engineer to support commissioning, qualification, and validation activities within a regulated GMP environment. This role will focus on the qualification and validation of analytical laboratory instruments, computerized systems, and GMP equipment while ensuring compliance with GxP, data integrity, and validation lifecycle requirements .\n\nThe ideal candidate will have hands‑on experience with IQ/OQ/PQ execution, CQV/CSV activities, validation documentation, and GMP-regulated environments , along with strong technical writing and cross‑functional collaboration skills.\n\nKey Responsibilities\n\nSupport the qualification and validation of analytical laboratory instruments, computerized systems, and GMP equipment.\n\nDevelop, execute, review, and maintain validation lifecycle documentation .\n\nExecute IQ, OQ, and PQ protocols and qualification activities.\n\nEnsure calibration readiness, data integrity, and GMP compliance throughout qualification activities.\n\nCollaborate with Quality Control, Instrumentation, Engineering, Automation, QA, and system owners .\n\nSupport change controls, impact assessments, deviations, CAPAs, and validation protocols .\n\nUtilize the Kneat validation platform for documentation, workflow, and validation activities.\n\nMaintain inspection‑ready documentation in accordance with GxP requirements.\n\nSupport Computerized System Validation (CSV) and CQV activities, including qualification execution and documentation.\n\nIdentify and resolve qualification/validation issues while maintaining project timelines.\n\nQualifications\n\n3-5 years of CQV and/or CSV experience in a regulated industry preferred.\n\nHands‑on experience with IQ, OQ, and PQ execution.\n\nExperience qualifying analytical laboratory instruments and GMP equipment preferred.\n\nKnowledge of GMP/GxP, data integrity, and validation lifecycle requirements.\n\nExperience supporting change controls, deviations, CAPAs, and impact assessments .\n\nFamiliarity with Kneat or similar validation/document management platforms.\n\nStrong technical writing, documentation, organization, communication, and problem‑solving skills.\n\nAbility to work effectively with cross‑functional teams in a regulated environment.\n\nCompensation\n\nEstimated hourly range: $80.00-$85.00/hr (W-2).\n\nFinal rate within this range will be based on skills, experience, and interview results.\n\n#J-18808-Ljbffr","company":"JMD Technologies","rawCompany":"jmd technologies","city":"Sunriver","state":"OR","isRemote":false,"isActive":false,"createdAt":"2026-08-24T03:21:31.319Z","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":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"CQV Engineer - Commissioning, Qualification & Validation","description":"Employment Type: Contract\n\nDuration: 9 Months\n\nStatus: Accepting Candidates\n\nAbout the Role\nWe are seeking an experienced CQV Engineer to support commissioning, qualification, and validation activities within a regulated GMP environment. This role will focus on the qualification and validation of analytical laboratory instruments, computerized systems, and GMP equipment while ensuring compliance with GxP, data integrity, and validation lifecycle requirements .\n\nThe ideal candidate will have hands‑on experience with IQ/OQ/PQ execution, CQV/CSV activities, validation documentation, and GMP-regulated environments , along with strong technical writing and cross‑functional collaboration skills.\n\nKey Responsibilities\n\nSupport the qualification and validation of analytical laboratory instruments, computerized systems, and GMP equipment.\n\nDevelop, execute, review, and maintain validation lifecycle documentation .\n\nExecute IQ, OQ, and PQ protocols and qualification activities.\n\nEnsure calibration readiness, data integrity, and GMP compliance throughout qualification activities.\n\nCollaborate with Quality Control, Instrumentation, Engineering, Automation, QA, and system owners .\n\nSupport change controls, impact assessments, deviations, CAPAs, and validation protocols .\n\nUtilize the Kneat validation platform for documentation, workflow, and validation activities.\n\nMaintain inspection‑ready documentation in accordance with GxP requirements.\n\nSupport Computerized System Validation (CSV) and CQV activities, including qualification execution and documentation.\n\nIdentify and resolve qualification/validation issues while maintaining project timelines.\n\nQualifications\n\n3-5 years of CQV and/or CSV experience in a regulated industry preferred.\n\nHands‑on experience with IQ, OQ, and PQ execution.\n\nExperience qualifying analytical laboratory instruments and GMP equipment preferred.\n\nKnowledge of GMP/GxP, data integrity, and validation lifecycle requirements.\n\nExperience supporting change controls, deviations, CAPAs, and impact assessments .\n\nFamiliarity with Kneat or similar validation/document management platforms.\n\nStrong technical writing, documentation, organization, communication, and problem‑solving skills.\n\nAbility to work effectively with cross‑functional teams in a regulated environment.\n\nCompensation\n\nEstimated hourly range: $80.00-$85.00/hr (W-2).\n\nFinal rate within this range will be based on skills, experience, and interview results.\n\n#J-18808-Ljbffr","datePosted":"2026-08-24T03:21:31.319Z","dateModified":"2026-08-24T03:21:31.319Z","hiringOrganization":{"@type":"Organization","name":"JMD Technologies","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Sunriver","addressRegion":"OR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"68eecf94e1be6d8ecf266432"},"url":"https://jobsearcher.com/jobs/68eecf94e1be6d8ecf266432"}}