{"schemaVersion":"jobsearcher.job.v1","id":"52e8d6dcfac492b9013e5d2a","url":"https://jobsearcher.com/jobs/52e8d6dcfac492b9013e5d2a","canonicalUrl":"https://jobsearcher.com/jobs/52e8d6dcfac492b9013e5d2a","title":"Validation Engineer","description":"For Quality Engineering - Global Manufacturing Operations services in the Manufacturing area.\nWHAT MAKES YOU A FIT:\nThe Technical Part:\nBachelor’s Degree in Engineering or Life Sciences and three (3) to five (5) years of exposure to Quality Validations within the regulated industry.\nLean Six Sigma certification preferred.\nBilingual English/Spanish, both written and verbal\nShift: Administrative and according to business needs.\nExperience in:\nDeveloping, Executing, and Reviewing Validations Life Cycles Protocols.\nTesting and Development of Statistical Process Control.\nMedical Device industry is a definite plus.\nValidation design, testing and development of statistical process control and monitoring.\nProduct design, costing and production requirements.\nThe Personality Part:\nOur Next Piece is someone who treats everyone they meet like family, especially our resources, clients and team members. In other words, being a customer service pro is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to take on this new challenge?\nAS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)\nAble to evaluate systems, implement validation packets, and identify existing or potential gaps\nProvides validation to technology/manufacturing systems in support of manufacturing sites for in-line products and processes\nProvides tactical direction and guidance for project teams implementing various activities for new and existing GMP systems.\nDevelops and reviews Standard Operating Procedures (SOPs).\nProvides support for ongoing compliance initiatives, assessments, corrective actions, and training.\nBased on equipment capabilities, generate and execute quality validation protocols (IQ, TMV, TQF, Process Characterization, and Process Validation).\nConduct validation of process equipment installation/operational/performance qualification studies to test their functionality.\nPrepare operational qualification assessments to support the fact that validated critical operating parameters are within qualified parameters.\nIdentify and evaluate equipment enhancements to support intended qualified operational ranges.\nSupport the evaluation of Change Controls to establish qualification assessments and performance qualification requirements during process and/or equipment modifications.\nSupport process capability and statistical analysis related to equipment performance.\nWHO WE ARE:\nWe are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS!\nAre you the next piece?\nxmOtF1LbEu","company":"Flexible Integrated Technical Services","rawCompany":"flexible integrated technical services","city":"Diaz","state":"AR","isRemote":false,"isActive":false,"createdAt":"2026-07-19T14:01:12.594Z","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":"334513","title":"Instruments and Related Products Manufacturing for Measuring, Displaying, and Controlling Industrial Process Variables","slug":"instruments-and-related-products-manufacturing-for-measuring-displaying-and-controlling-industrial-process-variables"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"For Quality Engineering - Global Manufacturing Operations services in the Manufacturing area.\nWHAT MAKES YOU A FIT:\nThe Technical Part:\nBachelor’s Degree in Engineering or Life Sciences and three (3) to five (5) years of exposure to Quality Validations within the regulated industry.\nLean Six Sigma certification preferred.\nBilingual English/Spanish, both written and verbal\nShift: Administrative and according to business needs.\nExperience in:\nDeveloping, Executing, and Reviewing Validations Life Cycles Protocols.\nTesting and Development of Statistical Process Control.\nMedical Device industry is a definite plus.\nValidation design, testing and development of statistical process control and monitoring.\nProduct design, costing and production requirements.\nThe Personality Part:\nOur Next Piece is someone who treats everyone they meet like family, especially our resources, clients and team members. In other words, being a customer service pro is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to take on this new challenge?\nAS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)\nAble to evaluate systems, implement validation packets, and identify existing or potential gaps\nProvides validation to technology/manufacturing systems in support of manufacturing sites for in-line products and processes\nProvides tactical direction and guidance for project teams implementing various activities for new and existing GMP systems.\nDevelops and reviews Standard Operating Procedures (SOPs).\nProvides support for ongoing compliance initiatives, assessments, corrective actions, and training.\nBased on equipment capabilities, generate and execute quality validation protocols (IQ, TMV, TQF, Process Characterization, and Process Validation).\nConduct validation of process equipment installation/operational/performance qualification studies to test their functionality.\nPrepare operational qualification assessments to support the fact that validated critical operating parameters are within qualified parameters.\nIdentify and evaluate equipment enhancements to support intended qualified operational ranges.\nSupport the evaluation of Change Controls to establish qualification assessments and performance qualification requirements during process and/or equipment modifications.\nSupport process capability and statistical analysis related to equipment performance.\nWHO WE ARE:\nWe are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS!\nAre you the next piece?\nxmOtF1LbEu","datePosted":"2026-07-19T14:01:12.594Z","dateModified":"2026-07-19T14:01:12.594Z","hiringOrganization":{"@type":"Organization","name":"Flexible Integrated Technical Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Diaz","addressRegion":"AR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"52e8d6dcfac492b9013e5d2a"},"url":"https://jobsearcher.com/jobs/52e8d6dcfac492b9013e5d2a"}}