{"schemaVersion":"jobsearcher.job.v1","id":"d1111f3808cfbd56b1f04927","url":"https://jobsearcher.com/jobs/d1111f3808cfbd56b1f04927","canonicalUrl":"https://jobsearcher.com/jobs/d1111f3808cfbd56b1f04927","title":"Quality Engineer","description":"If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.\n\nQuality Engineer\nFull Time Mount Prospect, IL, US\n\n3 days ago Requisition ID: 1014\n\nOur Solutions Protect Patients!\n\nFounded in 1932, Xttrium Laboratories has been dedicated to promoting health and well-being through high-quality products. Recognized as a trusted supplier of disinfectants to hospitals and healthcare providers, Xttrium has expanded its offerings to pharmacies nationwide. With over 40 years of expertise in manufacturing FDA-registered healthcare solutions, the company is a leader in ensuring safety and quality in a health-conscious world.\n\nWe are seeking a skilled and detail-oriented Quality Validation Engineer to assist with equipment validations in pharmaceutical manufacturing. The successful candidate will ensure compliance with industry regulations by executing and overseeing equipment qualification processes, including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Factory Acceptance Tests (FATs), Site Acceptance Tests (SATs), Cleaning Commissions, and Cleaning Validations. Additionally, this individual will be responsible for onboarding new equipment into the quality system. The role focuses on creating, reviewing, and executing validation documents and protocols to ensure our manufacturing processes and facilities meet the highest quality standards.\n\nResponsibilities\n\nDevelop and design detailed validation documents, including User Requirements Specifications (URS), IQ, OQ, PQ, and process validation protocols.\n\nConduct comprehensive process validations and facility qualifications to ensure manufacturing processes adhere to company and regulatory standards.\n\nLead cleaning validation efforts to ensure equipment cleaning processes meet regulatory and company standards for preventing cross-contamination and maintaining product integrity.\n\nOversee facility qualification activities, ensuring all equipment and infrastructure meet necessary requirements and comply with validation standards.\n\nDraft and finalize validation reports, summarizing the results of tests, inspections, and data analyses to support quality and compliance efforts.\n\nWork closely with production, quality control, and regulatory teams to ensure all validation efforts align with regulatory standards and company policies.\n\nBachelor’s degree in Engineering, Validation, or a related field within chemistry, biology, physics, etc.\n\n3-5 years of experience in validation within a pharmaceutical manufacturing environment.\n\nStrong understanding of validation protocols and documentation, including URS, IQ, OQ, PQ.\n\nExcellent written and verbal communication skills, with experience writing clear, concise reports.\n\nFamiliarity with pharmaceutical regulatory requirements and standards (e.g., FDA, ISO).\n\nAdditional Skills & Qualifications\n\nExperience with compounding and packaging of liquid drug products (highly preferred).\n\nExperience with validation of computer systems (preferred).\n\nExperience with serialization (preferred).\n\nWe are proud to be an Equal Opportunity Employer. We welcome people of all backgrounds, experiences, and perspectives. Employment decisions are made based on skills, qualifications, and potential; never on race, color, religion, sex, national origin, age, disability, veteran status, or any other protected trait.\n\nExpected compensation for this role will be between $100,000 and 115,000 on a full-time basis plus applicable health and ancillary benefits offered by the company. Actual compensation will range depending on a number of factors.\n\n#J-18808-Ljbffr","company":"Evolving Solution Services","rawCompany":"evolving solution services","city":"Mt Prospect","state":"IL","isRemote":false,"isActive":true,"createdAt":"2026-09-14T03:37:58.798Z","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":"Quality Engineer","description":"If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.\n\nQuality Engineer\nFull Time Mount Prospect, IL, US\n\n3 days ago Requisition ID: 1014\n\nOur Solutions Protect Patients!\n\nFounded in 1932, Xttrium Laboratories has been dedicated to promoting health and well-being through high-quality products. Recognized as a trusted supplier of disinfectants to hospitals and healthcare providers, Xttrium has expanded its offerings to pharmacies nationwide. With over 40 years of expertise in manufacturing FDA-registered healthcare solutions, the company is a leader in ensuring safety and quality in a health-conscious world.\n\nWe are seeking a skilled and detail-oriented Quality Validation Engineer to assist with equipment validations in pharmaceutical manufacturing. The successful candidate will ensure compliance with industry regulations by executing and overseeing equipment qualification processes, including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Factory Acceptance Tests (FATs), Site Acceptance Tests (SATs), Cleaning Commissions, and Cleaning Validations. Additionally, this individual will be responsible for onboarding new equipment into the quality system. The role focuses on creating, reviewing, and executing validation documents and protocols to ensure our manufacturing processes and facilities meet the highest quality standards.\n\nResponsibilities\n\nDevelop and design detailed validation documents, including User Requirements Specifications (URS), IQ, OQ, PQ, and process validation protocols.\n\nConduct comprehensive process validations and facility qualifications to ensure manufacturing processes adhere to company and regulatory standards.\n\nLead cleaning validation efforts to ensure equipment cleaning processes meet regulatory and company standards for preventing cross-contamination and maintaining product integrity.\n\nOversee facility qualification activities, ensuring all equipment and infrastructure meet necessary requirements and comply with validation standards.\n\nDraft and finalize validation reports, summarizing the results of tests, inspections, and data analyses to support quality and compliance efforts.\n\nWork closely with production, quality control, and regulatory teams to ensure all validation efforts align with regulatory standards and company policies.\n\nBachelor’s degree in Engineering, Validation, or a related field within chemistry, biology, physics, etc.\n\n3-5 years of experience in validation within a pharmaceutical manufacturing environment.\n\nStrong understanding of validation protocols and documentation, including URS, IQ, OQ, PQ.\n\nExcellent written and verbal communication skills, with experience writing clear, concise reports.\n\nFamiliarity with pharmaceutical regulatory requirements and standards (e.g., FDA, ISO).\n\nAdditional Skills & Qualifications\n\nExperience with compounding and packaging of liquid drug products (highly preferred).\n\nExperience with validation of computer systems (preferred).\n\nExperience with serialization (preferred).\n\nWe are proud to be an Equal Opportunity Employer. We welcome people of all backgrounds, experiences, and perspectives. Employment decisions are made based on skills, qualifications, and potential; never on race, color, religion, sex, national origin, age, disability, veteran status, or any other protected trait.\n\nExpected compensation for this role will be between $100,000 and 115,000 on a full-time basis plus applicable health and ancillary benefits offered by the company. Actual compensation will range depending on a number of factors.\n\n#J-18808-Ljbffr","datePosted":"2026-09-14T03:37:58.798Z","dateModified":"2026-09-14T03:37:58.798Z","hiringOrganization":{"@type":"Organization","name":"Evolving Solution Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Mt Prospect","addressRegion":"IL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d1111f3808cfbd56b1f04927"},"url":"https://jobsearcher.com/jobs/d1111f3808cfbd56b1f04927"}}