{"schemaVersion":"jobsearcher.job.v1","id":"c3c2628d911f6d10b829a1ee","url":"https://jobsearcher.com/jobs/c3c2628d911f6d10b829a1ee","canonicalUrl":"https://jobsearcher.com/jobs/c3c2628d911f6d10b829a1ee","title":"Process Validation Engineer","description":"we are in the pharmaceutical industry and looking for Process Validation support for manufacturing of fill/finish products.\nDay-to-Day Responsibilities\nwe are looking for a process validation engineer who can generate process validation protocols, summary reports and understand what documentation is required from CQV through the process validation lifecycle.\nYou should have a great understanding of what critical process parameters are vs. non-critical process parameters.\nIt is required to be able to support PV readiness, complete risk assessments and own Process Validations from end to end.\nYou will be providing the oversight of batch executions/manufacturing from a process validation perspective in order to be able to raise concerns throughout the process and correct as needed.\nJob Types: Contract, Full-time\nPay: $50.00 per hour\nSchedule:\n8 hour shift\nDay shift\nEducation:\nBachelor's (Required)\nExperience:\nprocess validation: 2 years (Required)\nCQV: 2 years (Required)\nValidation protocols: 1 year (Required)\nCritical process parameter: 1 year (Required)\nPV readiness: 1 year (Required)\nWork Location: In person","company":"Ar Val Services","rawCompany":"ar val services","city":"Allen","state":"TX","isRemote":false,"isActive":false,"createdAt":"2026-04-12T20:19:25.501Z","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":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325411","title":"Medicinal and Botanical Manufacturing","slug":"medicinal-and-botanical-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Validation Engineer","description":"we are in the pharmaceutical industry and looking for Process Validation support for manufacturing of fill/finish products.\nDay-to-Day Responsibilities\nwe are looking for a process validation engineer who can generate process validation protocols, summary reports and understand what documentation is required from CQV through the process validation lifecycle.\nYou should have a great understanding of what critical process parameters are vs. non-critical process parameters.\nIt is required to be able to support PV readiness, complete risk assessments and own Process Validations from end to end.\nYou will be providing the oversight of batch executions/manufacturing from a process validation perspective in order to be able to raise concerns throughout the process and correct as needed.\nJob Types: Contract, Full-time\nPay: $50.00 per hour\nSchedule:\n8 hour shift\nDay shift\nEducation:\nBachelor's (Required)\nExperience:\nprocess validation: 2 years (Required)\nCQV: 2 years (Required)\nValidation protocols: 1 year (Required)\nCritical process parameter: 1 year (Required)\nPV readiness: 1 year (Required)\nWork Location: In person","datePosted":"2026-04-12T20:19:25.501Z","dateModified":"2026-04-12T20:19:25.501Z","hiringOrganization":{"@type":"Organization","name":"Ar Val Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Allen","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"c3c2628d911f6d10b829a1ee"},"url":"https://jobsearcher.com/jobs/c3c2628d911f6d10b829a1ee"}}