{"schemaVersion":"jobsearcher.job.v1","id":"e7f83a85f67074e248386d6a","url":"https://jobsearcher.com/jobs/e7f83a85f67074e248386d6a","canonicalUrl":"https://jobsearcher.com/jobs/e7f83a85f67074e248386d6a","title":"Process Engineer - Pharma","description":"Job Title: Process Engineer – PharmaLocation: Cincinnati, OH (Onsite)Duration: 12 Months ContractPosition Summary:We are seeking an experienced Process Engineer – Solid Dosage to provide hands-on manufacturing support for commercial pharmaceutical production. This role will focus on shop floor support, process optimization, PPQ activities, and technology transfer to ensure successful product launches and reliable commercial manufacturing.Key Responsibilities:Provide day-to-day manufacturing support for commercial solid dosage production.Support PPQ (Process Performance Qualification) batches and validation activities.Serve as the primary shop floor technical resource during manufacturing operations.Support technology transfer activities from development to commercial manufacturing.Troubleshoot manufacturing and process issues to ensure successful batch execution.Collaborate with Manufacturing, Quality, Validation, and Engineering teams.Review manufacturing documentation, protocols, and batch records.Ensure compliance with cGMP and company quality standards.Required Qualifications:Bachelor's degree in Engineering, Pharmaceutical Sciences, or a related discipline.Experience supporting commercial pharmaceutical manufacturing.Hands-on experience with Solid Oral Dosage (OSD) manufacturing.Strong knowledge of cGMP regulations.Excellent troubleshooting and problem-solving skills.Strong communication and cross-functional collaboration skills.Required Process & Equipment Experience:Tablet CompressionTablet Film CoatingRoller CompactionGranulationCommercial Drug Product (DP) ManufacturingPPQ / Process ValidationTechnology Transfer","company":"Intellectt","rawCompany":"intellectt","city":"Oh","state":"EN","isRemote":false,"isActive":false,"createdAt":"2026-07-08T07:45:39.716Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325411","title":"Medicinal and Botanical Manufacturing","slug":"medicinal-and-botanical-manufacturing"},{"code":"424210","title":"Drugs and Druggists' Sundries Merchant Wholesalers","slug":"drugs-and-druggists-sundries-merchant-wholesalers"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer - Pharma","description":"Job Title: Process Engineer – PharmaLocation: Cincinnati, OH (Onsite)Duration: 12 Months ContractPosition Summary:We are seeking an experienced Process Engineer – Solid Dosage to provide hands-on manufacturing support for commercial pharmaceutical production. This role will focus on shop floor support, process optimization, PPQ activities, and technology transfer to ensure successful product launches and reliable commercial manufacturing.Key Responsibilities:Provide day-to-day manufacturing support for commercial solid dosage production.Support PPQ (Process Performance Qualification) batches and validation activities.Serve as the primary shop floor technical resource during manufacturing operations.Support technology transfer activities from development to commercial manufacturing.Troubleshoot manufacturing and process issues to ensure successful batch execution.Collaborate with Manufacturing, Quality, Validation, and Engineering teams.Review manufacturing documentation, protocols, and batch records.Ensure compliance with cGMP and company quality standards.Required Qualifications:Bachelor's degree in Engineering, Pharmaceutical Sciences, or a related discipline.Experience supporting commercial pharmaceutical manufacturing.Hands-on experience with Solid Oral Dosage (OSD) manufacturing.Strong knowledge of cGMP regulations.Excellent troubleshooting and problem-solving skills.Strong communication and cross-functional collaboration skills.Required Process & Equipment Experience:Tablet CompressionTablet Film CoatingRoller CompactionGranulationCommercial Drug Product (DP) ManufacturingPPQ / Process ValidationTechnology Transfer","datePosted":"2026-07-08T07:45:39.716Z","dateModified":"2026-07-08T07:45:39.716Z","hiringOrganization":{"@type":"Organization","name":"Intellectt","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Oh","addressRegion":"EN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"e7f83a85f67074e248386d6a"},"url":"https://jobsearcher.com/jobs/e7f83a85f67074e248386d6a"}}