{"schemaVersion":"jobsearcher.job.v1","id":"4fca8908df15a4871247733d","url":"https://jobsearcher.com/jobs/4fca8908df15a4871247733d","canonicalUrl":"https://jobsearcher.com/jobs/4fca8908df15a4871247733d","title":"Process Engineer – Equipment Validation & Packaging Systems","description":"Job Title: Process Engineer – Equipment Validation & Packaging SystemsLocation: Columbus, OH (Onsite – Overnight Shift)Employment: ContractJob DescriptionWe are seeking an experienced Process Engineer with 4-7 years of pharmaceutical or biopharmaceutical manufacturing experience to support equipment validation, qualification, and process engineering activities for commercial packaging operations. The ideal candidate will have strong hands-on experience with IQ/OQ/PQ, equipment characterization, requalification, automated packaging equipment, and GMP-regulated manufacturing environments.Required Skills & Experience4-7 years of experience in pharmaceutical/biopharmaceutical manufacturing.Hands-on experience with Equipment Validation & Qualification (IQ/OQ/PQ).Experience performing equipment characterization studies and equipment requalification.Strong knowledge of validation protocol development and execution.Experience supporting pharmaceutical packaging lines and automated packaging equipment.Hands-on troubleshooting and optimization of packaging equipment in GMP/cGMP environments.Experience with serialization systems, labeling systems, conveyors, palletizers, case packers, Cognex vision systems, or similar automated packaging equipment.Knowledge of CAPA, Root Cause Analysis, Change Control, and Continuous Improvement.Ability to collaborate with Manufacturing, Quality, Validation, and Maintenance teams.Bachelor's degree in Mechanical Engineering preferred (or Chemical, Industrial, Manufacturing Engineering, or related discipline).","company":"Shoolin","rawCompany":"shoolin","city":"Oh","state":"EN","isRemote":false,"isActive":false,"createdAt":"2026-08-05T09:44:53.764Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"51-9111.00","title":"Packaging and Filling Machine Operators and Tenders","slug":"packaging-and-filling-machine-operators-and-tenders"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"561910","title":"Packaging and Labeling Services","slug":"packaging-and-labeling-services"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer – Equipment Validation & Packaging Systems","description":"Job Title: Process Engineer – Equipment Validation & Packaging SystemsLocation: Columbus, OH (Onsite – Overnight Shift)Employment: ContractJob DescriptionWe are seeking an experienced Process Engineer with 4-7 years of pharmaceutical or biopharmaceutical manufacturing experience to support equipment validation, qualification, and process engineering activities for commercial packaging operations. The ideal candidate will have strong hands-on experience with IQ/OQ/PQ, equipment characterization, requalification, automated packaging equipment, and GMP-regulated manufacturing environments.Required Skills & Experience4-7 years of experience in pharmaceutical/biopharmaceutical manufacturing.Hands-on experience with Equipment Validation & Qualification (IQ/OQ/PQ).Experience performing equipment characterization studies and equipment requalification.Strong knowledge of validation protocol development and execution.Experience supporting pharmaceutical packaging lines and automated packaging equipment.Hands-on troubleshooting and optimization of packaging equipment in GMP/cGMP environments.Experience with serialization systems, labeling systems, conveyors, palletizers, case packers, Cognex vision systems, or similar automated packaging equipment.Knowledge of CAPA, Root Cause Analysis, Change Control, and Continuous Improvement.Ability to collaborate with Manufacturing, Quality, Validation, and Maintenance teams.Bachelor's degree in Mechanical Engineering preferred (or Chemical, Industrial, Manufacturing Engineering, or related discipline).","datePosted":"2026-08-05T09:44:53.764Z","dateModified":"2026-08-05T09:44:53.764Z","hiringOrganization":{"@type":"Organization","name":"Shoolin","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Oh","addressRegion":"EN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"4fca8908df15a4871247733d"},"url":"https://jobsearcher.com/jobs/4fca8908df15a4871247733d"}}