{"schemaVersion":"jobsearcher.job.v1","id":"8a0fcd332ce5846f3209f0a4","url":"https://jobsearcher.com/jobs/8a0fcd332ce5846f3209f0a4","canonicalUrl":"https://jobsearcher.com/jobs/8a0fcd332ce5846f3209f0a4","title":"Primary Loop Process Engineer","description":"Process Engineer (Day Shift) This role focuses on providing technical and on‑floor support for process and equipment, ensuring compliance with cGMP standards, and driving process optimization.\nResponsibilities Provide technical and on‑floor support for process and equipment by troubleshooting issues, assisting manufacturing teams, documenting problems in the quality management system, performing root cause analysis, and implementing corrective and preventive actions.\nEnsure equipment qualification and compliance with cGMP standards, company policies, and regulatory requirements; oversee interventions, maintenance, and changes with documentation through formal change control.\nDrive performance and process optimization through data analysis to monitor equipment/process performance, assess capacity, and identify continuous improvement opportunities.\nLead and support the full lifecycle of capital projects (design, development, execution, commissioning, qualification, validation), including scope, design alternatives, equipment selection, user requirements, construction oversight, and process validation support.\nDevelop and manage technical documentation and risk mitigation (user requirements, P&IDs, safety/environmental assessments, qualification protocols) and collaborate cross‑functionally to identify risks and support value engineering.\nMinimum qualifications Bachelor’s degree in Chemical, Biological, or related engineering discipline.\nExperience in pharmaceutical, biotechnology, or a related/relevant industry.\nKnowledge of cGMP and/or experience in a regulated environment; success working in cross‑functional teams.\nPreferred qualifications 2+ years of relevant industry experience.\nExperience with capital project design/development/execution.\nUnderstanding of monoclonal antibody/recombinant protein manufacturing processes.\nExperience with SAP EAM, ERP, AutoCAD, Veeva Vault, AVEVA PI, Seeq, Meridian.\nUnderstanding and application of RCI, FMEA, and QRM tools.\nWorking knowledge of USDA and/or EU GMP regulations for veterinary biologics.\nBenefits Relocation packages; two‑week shutdowns (mid‑summer and year‑end) in addition to PTO; 8‑week parental leave; 9 Employee Resource Groups; annual bonus; up to 6% 401K matching.\nAdditional information Location: Elwood, KS.\nSalaried day shift; weekend work required on rotation for process support.\n\n#J-18808-Ljbffr","company":"Scorpion Therapeutics","rawCompany":"scorpion therapeutics","city":"Wathena","state":"KS","isRemote":false,"isActive":false,"createdAt":"2026-06-17T03:44:20.112Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"},{"code":"17-2041.00","title":"Chemical Engineers","slug":"chemical-engineers"}],"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":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Primary Loop Process Engineer","description":"Process Engineer (Day Shift) This role focuses on providing technical and on‑floor support for process and equipment, ensuring compliance with cGMP standards, and driving process optimization.\nResponsibilities Provide technical and on‑floor support for process and equipment by troubleshooting issues, assisting manufacturing teams, documenting problems in the quality management system, performing root cause analysis, and implementing corrective and preventive actions.\nEnsure equipment qualification and compliance with cGMP standards, company policies, and regulatory requirements; oversee interventions, maintenance, and changes with documentation through formal change control.\nDrive performance and process optimization through data analysis to monitor equipment/process performance, assess capacity, and identify continuous improvement opportunities.\nLead and support the full lifecycle of capital projects (design, development, execution, commissioning, qualification, validation), including scope, design alternatives, equipment selection, user requirements, construction oversight, and process validation support.\nDevelop and manage technical documentation and risk mitigation (user requirements, P&IDs, safety/environmental assessments, qualification protocols) and collaborate cross‑functionally to identify risks and support value engineering.\nMinimum qualifications Bachelor’s degree in Chemical, Biological, or related engineering discipline.\nExperience in pharmaceutical, biotechnology, or a related/relevant industry.\nKnowledge of cGMP and/or experience in a regulated environment; success working in cross‑functional teams.\nPreferred qualifications 2+ years of relevant industry experience.\nExperience with capital project design/development/execution.\nUnderstanding of monoclonal antibody/recombinant protein manufacturing processes.\nExperience with SAP EAM, ERP, AutoCAD, Veeva Vault, AVEVA PI, Seeq, Meridian.\nUnderstanding and application of RCI, FMEA, and QRM tools.\nWorking knowledge of USDA and/or EU GMP regulations for veterinary biologics.\nBenefits Relocation packages; two‑week shutdowns (mid‑summer and year‑end) in addition to PTO; 8‑week parental leave; 9 Employee Resource Groups; annual bonus; up to 6% 401K matching.\nAdditional information Location: Elwood, KS.\nSalaried day shift; weekend work required on rotation for process support.\n\n#J-18808-Ljbffr","datePosted":"2026-06-17T03:44:20.112Z","dateModified":"2026-06-17T03:44:20.112Z","hiringOrganization":{"@type":"Organization","name":"Scorpion Therapeutics","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Wathena","addressRegion":"KS","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"8a0fcd332ce5846f3209f0a4"},"url":"https://jobsearcher.com/jobs/8a0fcd332ce5846f3209f0a4"}}