{"schemaVersion":"jobsearcher.job.v1","id":"f784a1abdc4cd7a6427fcc15","url":"https://jobsearcher.com/jobs/f784a1abdc4cd7a6427fcc15","canonicalUrl":"https://jobsearcher.com/jobs/f784a1abdc4cd7a6427fcc15","title":"Validation Engineer","description":"Become a part of our industry-leading and engineering-driven precision injection molding company.In business for over four decades, our expansive facilities, specialized machinery, and expert team members\nare representative of the top-notch work environment you’ll find at Chemtech Plastics.\n\nMeet the Chemtech Team\nBENEFITS\nEmployee benefits are a top priority at Chemtech Plastics, which is why we've c reated a comprehensive benefits package to support you in your personal life and future planning. T his includes competitive pay, life insurance, continuing education assistance, 401K, and more.\n\nEmployer matching\n\nHealth\n\nVision\n\nPaid Vacation\n\nDisability (Short- and Long-Term)\n\nCurrent Openings\nPosition: Validation Engineer\n\nLocation: Elgin, IL\n\nJob Id: 183\n\n# of Openings: 1\n\nValidation Engineer\n\n1st shift\n\nE-Verify\n\nDuties/Responsibilities\n\nParticipate in projects/program management, review new and existing drawings as received from customers and evaluate potential quality issues.\n\nDevelop and execute IQ, OQ, and PQ validation protocols for production processes, equipment and software in a timely and cost-effective manner.\n\nWrite reports summarizing results for equipment, process or software validation projects.\n\nDetermine deliverables with the customer and cost estimate the sampling requirements and inspection activity.\n\nReview existing validation reports and identify/mitigate gaps for compliance to requirements\n\nWork with Q.A. Dept. on piece part inspections and capability studies of new mold and engineering changes to ensure all requirements are completed and approved.\n\nConduct or lead corrective and preventive actions in quality systems or validations using problem solving techniques.\n\nParticipate as an active new product development core team member.\n\nProcess all stages of validation documents and oversee the completion and signatures.\n\nSupport quality system projects and activities such as engineering change order support and complaint investigation support.\n\nSupport FDA inspection readiness activities.\n\nInterfacing customers, staff and fellow managers to establish and maintain validation schedules throughout the company.\n\nAbility to interact with customers in all necessary situations to keep them informed of progress and documentation status.\n\nConsults with customers on quality and inspection-related issues.\n\nManages and holds project meetings with customers.\n\nOther duties as assigned by the Director of Engineering.\n\nRequired Skills/Abilities\n\nExcellent written and verbal communication skills and highly effective time management skills.\n\nAbility to operate independently and as part of a team\n\nIndependent problem-solving skills\n\nProficient in root cause analysis, verification & validation, process flow mapping\n\nTechnical and procedural understanding of customer requirements for part validation.\n\nProject management skills include planning, processing, organizing and tracking of all part validation activities.\n\nExperience processing data in MiniTab software and correlate P values.\n\nKnowledge of processes and procedures for cost estimating of validation work.\n\nEducation and Experience:\n\nBachelor of Science degree from an accredited college or university in an Engineering or Science discipline and 3-5 years of process/software validation experience in a regulated industry\n\nWorking knowledge of Medical Device Regulations and Standards (FDA, ISO 13485, ISO 14971, MDD, IVDD)\n\nPhysical Requirements:\n\nProlonged periods sitting at a desk and working on a computer.\n\nMust be able to lift 15 lbs.\n\nMust be able to access and navigate each department at the organization’s facilities.\n\nBenefits and Compensation\n\nFull benefit offerings including medical, dental, vision, and voluntary plans\n\nDQS-Certified for IATF 16949 : 2016 and ISO 9001 : 2015\n\n#J-18808-Ljbffr","company":"Chemtech Plastics","rawCompany":"chemtech plastics","city":"Carol Stream","state":"IL","isRemote":false,"isActive":false,"createdAt":"2026-06-17T03:38:23.641Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"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":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"Become a part of our industry-leading and engineering-driven precision injection molding company.In business for over four decades, our expansive facilities, specialized machinery, and expert team members\nare representative of the top-notch work environment you’ll find at Chemtech Plastics.\n\nMeet the Chemtech Team\nBENEFITS\nEmployee benefits are a top priority at Chemtech Plastics, which is why we've c reated a comprehensive benefits package to support you in your personal life and future planning. T his includes competitive pay, life insurance, continuing education assistance, 401K, and more.\n\nEmployer matching\n\nHealth\n\nVision\n\nPaid Vacation\n\nDisability (Short- and Long-Term)\n\nCurrent Openings\nPosition: Validation Engineer\n\nLocation: Elgin, IL\n\nJob Id: 183\n\n# of Openings: 1\n\nValidation Engineer\n\n1st shift\n\nE-Verify\n\nDuties/Responsibilities\n\nParticipate in projects/program management, review new and existing drawings as received from customers and evaluate potential quality issues.\n\nDevelop and execute IQ, OQ, and PQ validation protocols for production processes, equipment and software in a timely and cost-effective manner.\n\nWrite reports summarizing results for equipment, process or software validation projects.\n\nDetermine deliverables with the customer and cost estimate the sampling requirements and inspection activity.\n\nReview existing validation reports and identify/mitigate gaps for compliance to requirements\n\nWork with Q.A. Dept. on piece part inspections and capability studies of new mold and engineering changes to ensure all requirements are completed and approved.\n\nConduct or lead corrective and preventive actions in quality systems or validations using problem solving techniques.\n\nParticipate as an active new product development core team member.\n\nProcess all stages of validation documents and oversee the completion and signatures.\n\nSupport quality system projects and activities such as engineering change order support and complaint investigation support.\n\nSupport FDA inspection readiness activities.\n\nInterfacing customers, staff and fellow managers to establish and maintain validation schedules throughout the company.\n\nAbility to interact with customers in all necessary situations to keep them informed of progress and documentation status.\n\nConsults with customers on quality and inspection-related issues.\n\nManages and holds project meetings with customers.\n\nOther duties as assigned by the Director of Engineering.\n\nRequired Skills/Abilities\n\nExcellent written and verbal communication skills and highly effective time management skills.\n\nAbility to operate independently and as part of a team\n\nIndependent problem-solving skills\n\nProficient in root cause analysis, verification & validation, process flow mapping\n\nTechnical and procedural understanding of customer requirements for part validation.\n\nProject management skills include planning, processing, organizing and tracking of all part validation activities.\n\nExperience processing data in MiniTab software and correlate P values.\n\nKnowledge of processes and procedures for cost estimating of validation work.\n\nEducation and Experience:\n\nBachelor of Science degree from an accredited college or university in an Engineering or Science discipline and 3-5 years of process/software validation experience in a regulated industry\n\nWorking knowledge of Medical Device Regulations and Standards (FDA, ISO 13485, ISO 14971, MDD, IVDD)\n\nPhysical Requirements:\n\nProlonged periods sitting at a desk and working on a computer.\n\nMust be able to lift 15 lbs.\n\nMust be able to access and navigate each department at the organization’s facilities.\n\nBenefits and Compensation\n\nFull benefit offerings including medical, dental, vision, and voluntary plans\n\nDQS-Certified for IATF 16949 : 2016 and ISO 9001 : 2015\n\n#J-18808-Ljbffr","datePosted":"2026-06-17T03:38:23.641Z","dateModified":"2026-06-17T03:38:23.641Z","hiringOrganization":{"@type":"Organization","name":"Chemtech Plastics","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Carol Stream","addressRegion":"IL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"f784a1abdc4cd7a6427fcc15"},"url":"https://jobsearcher.com/jobs/f784a1abdc4cd7a6427fcc15"}}