{"schemaVersion":"jobsearcher.job.v1","id":"2032fd844ddf952e8078002c","url":"https://jobsearcher.com/jobs/2032fd844ddf952e8078002c","canonicalUrl":"https://jobsearcher.com/jobs/2032fd844ddf952e8078002c","title":"Process Engineer","description":"The Science Team at Pride Health is currently supporting a Life Sciences and Advanced Technology client that is looking to hire a Process Engineer in Paris, KY 40361.\n\nProcess Engineer\n\nParis, KY 40361\n\nDuration: 09+ Months\n\nPay rate: $50 - $54/Hr.\n\nSchedule: 8:00 AM – 5:00 PM, Monday–Friday (occasional 6:00 AM start), some overtime as needed.\n\nJob Description\nThe Process Engineer is accountable for providing engineering leadership and technical support to Avantor operations directly supporting manufacturing, product development, safety, and customer support. The Process Engineer leads manufacturing technology product, safety management process, and/or process development, scale-up, and implementation.\n\nIntake Notes – Process Engineer\n\nCandidates must have experience working in a pharmaceutical, chemical, or other highly regulated cGMP manufacturing environment.\n\nThis is a temp-to-possible-hire opportunity.\n\nStrong preference for candidates with experience manufacturing pharmaceutical solutions, solvents, or similar products.\n\nPosition will support capital projects involving both manufacturing equipment (hardware) and control systems/software.\n\nResponsible for maintaining and improving production line performance, equipment uptime, and operational efficiency.\n\nWill partner closely with Safety and Quality teams to identify and resolve manufacturing, compliance, and process-related challenges.\n\nExpected to troubleshoot equipment downtime issues and drive continuous improvement initiatives to keep production running efficiently.\n\nBachelor's degree in Engineering is required.\n\nSeeking candidates with 5–8 years of Process Engineering experience, ideally gained entirely within cGMP-regulated manufacturing environments.\n\nStrong communication and presentation skills are essential, as this individual will develop business cases, interact with vendors, and communicate recommendations to cross‑functional stakeholders.\n\nLooking for a hands‑on engineer who can effectively support day‑to‑day manufacturing operations while also contributing to larger capital and process improvement projects.\n\nMinimum Requirements\nEducation\n\nBachelor's Degree in Chemical Engineering or a related field required.\n\nKnowledge of basic problem‑solving tools (DMAIC) and lean manufacturing concepts (Kanban, Kaizen, 5S) required.\n\nExperience\n\nMinimum of five (5) years of related experience required.\n\nMinimum of two (2) years of experience working in a chemical manufacturing environment required.\n\nPreferred Qualifications\n\nSix Sigma Black Belt certification preferred.\n\nLean certification preferred.\n\nKnowledge of OSHA, NFPA, HazWoper, and other governmental regulatory requirements (e.g., 21 CFR Part 820, cGMP, ISO, FDA, etc.).\n\nSkills/Competencies\n\nGeneral knowledge of chemistry and high‑purity chemical processing/engineering and microelectronic applications required.\n\nDemonstrated complex problem‑solving expertise and experience.\n\nDemonstrated application and implementation of SPC tools.\n\nWorking knowledge and experience in:\nDistillation and separation purification technologies\n\nChemical synthesis unit operations\n\nProcess control\n\nEnvironmental control systems\n\nClean manufacturing\n\nWorking knowledge of financial/cost systems and standard operating procedures.\n\nKnowledge of FDA, cGMP, ISO 9000, and applicable state and federal environmental regulations.\n\nDemonstrated organizational, technical leadership, presentation, and communication skills.\n\nAbility to understand analytical procedures, quantify analytical results, and make adjustments and corrections as needed.\n\nAbility to partner effectively with all functions and levels of the organization.\n\nDetail‑oriented with strong analytical and problem‑solving skills.\n\nStrong sense of urgency, initiative, and drive.\n\nStrong organization and prioritization skills.\n\nOther Skills\n\nStrong competency in Microsoft Office, specifically PowerPoint, Excel, and Word.\n\nWorking Conditions\nThe work environment is a manufacturing facility, and appropriate PPE will be required in designated areas.\n\n#J-18808-Ljbffr","company":"Pride Global","rawCompany":"pride global","city":"Paris","state":"KY","isRemote":false,"isActive":false,"createdAt":"2026-07-08T03:33:29.138Z","occupations":[{"code":"17-2041.00","title":"Chemical Engineers","slug":"chemical-engineers"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"}],"industries":[{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325199","title":"All Other Basic Organic Chemical Manufacturing","slug":"all-other-basic-organic-chemical-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer","description":"The Science Team at Pride Health is currently supporting a Life Sciences and Advanced Technology client that is looking to hire a Process Engineer in Paris, KY 40361.\n\nProcess Engineer\n\nParis, KY 40361\n\nDuration: 09+ Months\n\nPay rate: $50 - $54/Hr.\n\nSchedule: 8:00 AM – 5:00 PM, Monday–Friday (occasional 6:00 AM start), some overtime as needed.\n\nJob Description\nThe Process Engineer is accountable for providing engineering leadership and technical support to Avantor operations directly supporting manufacturing, product development, safety, and customer support. The Process Engineer leads manufacturing technology product, safety management process, and/or process development, scale-up, and implementation.\n\nIntake Notes – Process Engineer\n\nCandidates must have experience working in a pharmaceutical, chemical, or other highly regulated cGMP manufacturing environment.\n\nThis is a temp-to-possible-hire opportunity.\n\nStrong preference for candidates with experience manufacturing pharmaceutical solutions, solvents, or similar products.\n\nPosition will support capital projects involving both manufacturing equipment (hardware) and control systems/software.\n\nResponsible for maintaining and improving production line performance, equipment uptime, and operational efficiency.\n\nWill partner closely with Safety and Quality teams to identify and resolve manufacturing, compliance, and process-related challenges.\n\nExpected to troubleshoot equipment downtime issues and drive continuous improvement initiatives to keep production running efficiently.\n\nBachelor's degree in Engineering is required.\n\nSeeking candidates with 5–8 years of Process Engineering experience, ideally gained entirely within cGMP-regulated manufacturing environments.\n\nStrong communication and presentation skills are essential, as this individual will develop business cases, interact with vendors, and communicate recommendations to cross‑functional stakeholders.\n\nLooking for a hands‑on engineer who can effectively support day‑to‑day manufacturing operations while also contributing to larger capital and process improvement projects.\n\nMinimum Requirements\nEducation\n\nBachelor's Degree in Chemical Engineering or a related field required.\n\nKnowledge of basic problem‑solving tools (DMAIC) and lean manufacturing concepts (Kanban, Kaizen, 5S) required.\n\nExperience\n\nMinimum of five (5) years of related experience required.\n\nMinimum of two (2) years of experience working in a chemical manufacturing environment required.\n\nPreferred Qualifications\n\nSix Sigma Black Belt certification preferred.\n\nLean certification preferred.\n\nKnowledge of OSHA, NFPA, HazWoper, and other governmental regulatory requirements (e.g., 21 CFR Part 820, cGMP, ISO, FDA, etc.).\n\nSkills/Competencies\n\nGeneral knowledge of chemistry and high‑purity chemical processing/engineering and microelectronic applications required.\n\nDemonstrated complex problem‑solving expertise and experience.\n\nDemonstrated application and implementation of SPC tools.\n\nWorking knowledge and experience in:\nDistillation and separation purification technologies\n\nChemical synthesis unit operations\n\nProcess control\n\nEnvironmental control systems\n\nClean manufacturing\n\nWorking knowledge of financial/cost systems and standard operating procedures.\n\nKnowledge of FDA, cGMP, ISO 9000, and applicable state and federal environmental regulations.\n\nDemonstrated organizational, technical leadership, presentation, and communication skills.\n\nAbility to understand analytical procedures, quantify analytical results, and make adjustments and corrections as needed.\n\nAbility to partner effectively with all functions and levels of the organization.\n\nDetail‑oriented with strong analytical and problem‑solving skills.\n\nStrong sense of urgency, initiative, and drive.\n\nStrong organization and prioritization skills.\n\nOther Skills\n\nStrong competency in Microsoft Office, specifically PowerPoint, Excel, and Word.\n\nWorking Conditions\nThe work environment is a manufacturing facility, and appropriate PPE will be required in designated areas.\n\n#J-18808-Ljbffr","datePosted":"2026-07-08T03:33:29.138Z","dateModified":"2026-07-08T03:33:29.138Z","hiringOrganization":{"@type":"Organization","name":"Pride Global","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Paris","addressRegion":"KY","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"2032fd844ddf952e8078002c"},"url":"https://jobsearcher.com/jobs/2032fd844ddf952e8078002c"}}