{"schemaVersion":"jobsearcher.job.v1","id":"ebddb61035a69952596db44c","url":"https://jobsearcher.com/jobs/ebddb61035a69952596db44c","canonicalUrl":"https://jobsearcher.com/jobs/ebddb61035a69952596db44c","title":"Process Engineer (Largo, FL)","description":"Primary Purpose\nProvide engineering services for full product life cycle including process robustness review, process optimization initiatives, product equipment transfers, process validations, cleaning validations, material changes, and commercial product manufacturing technical support.\n\nMajor Duties and Responsibilities\n\nIndependent management of product transfers, performing equipment fit and gap analyses, and authoring critical documentation such as Risk Assessment, OOS Investigation, Process Validation protocols, Cleaning Validation protocols, etc.\n\nFocused on process optimization in all phases of manufacturing process (blending, filling, packaging, etc) using lean or six sigma tools for optimal impact.\n\nLead and/or support cleaning validation and process validation efforts and projects, as needed to support commercial operations.\n\nIdentify and lead continuous improvement engineering projects to enhance process robustness, manufacturing efficiency, and deviation reduction through engineering controls.\n\nGenerate technical reports, specifications, and other supporting documentation as needed.\n\nCoordinate with outside vendors, contract labs, and equipment manufacturers as needed to support project or related work deliverables.\n\nProvide day-to-day technical support for commercial manufacturing. Conduct technical investigations, write reports, and aid in the close-out of deviations.\n\nSupport business with strategic analysis and proactive concept development for manufacturing process optimization projects.\n\nCollaborates across various departments like Manufacturing, Quality, R&D teams, Engineering, and Project Management to ensure project success.\n\nGenerate/maintain documents and provide related technical support related to GMP Manufacturing executions, product impact assessments and periodic reviews.\n\nParticipate in the project team meetings, decisions, and creation of milestones representing process engineering.\n\nProcess training, as needed, in adherence to company policies and quality requirements.\n\nEvaluate, define, and provide user requirements for process equipment associated with drug product manufacturing.\n\nPrepare and present data associated with manufacturing processes to internal and external teams as required.\n\nKeep current on regulatory and quality requirements for manufacturing, including FDA-regulated products and cGMP compliance.\n\nInteracts regularly with senior technical peers and colleagues.\n\nOther functions as required to support existing operations and client-driven projects.\n\nManufacturing, Science and Technology\n\nQualifications\n\nBachelor’s degree in chemical engineering or relevant experience (MS Preferred)\n\nAt least 5-10 years of process engineering/technical services/MS&T experience in the pharmaceutical/chemical manufacturing industry, preferably with cGMP manufacturing of FDA-regulated drug products.\n\nCritical Skills and Abilities\n\nDemonstrated ability for independent work, thought, and analysis.\n\nAbility to coordinate with internal groups as needed to achieve desired goals and deliverables (Manufacturing, Engineering, Supply chain, QA, QC, R&D, Project Management, etc.).\n\nExceptional time management and multi-tasking skills.\n\nExcellent written and verbal communication skills with expertise in good documentation practices.\n\nAbility to perform statistical analysis of data and interpretation of data.\n\nMust be able to work extended hours on evening and weekends as required.\n\nMust be capable of detailed recordkeeping and communicating results to others.\n\nExperience with pharmaceutical and consumer products related to creams, lotions, liquids, aerosols, nasal sprays, and/or gels is a plus.\n\nCleaning validation experience is strongly preferred.\n\nProcess validation experience is strongly preferred.\n\nComputer Skills\n\nProficient with Microsoft Office 365, including Teams, Word, Excel, and PowerPoint.\n\nMinitab experience is preferred but not required.\n\nPhysical Demands\n\nMust be able to lift and maneuver forty pounds.\n\nMust be capable of standing for extended periods of time.\n\nMust be able to wear personal protection equipment which includes gloves and respirator when required.\n\nAbility to perform work in a manufacturing environment where there is exposure to occupational hazards.\n\nMust be able to work extended hours on evenings and weekends as required.\n\nPersonal Information\n\nFirst name\n\nLast name\n\nEmail\n\nAddress\n\nCity\n\nState\n\nZip code\n\nPhone number\n\nAttachments\n\nAttach your Resume\n\nAttach Dropbox\n\nPaste Attach a Cover letter\n\nAttach Dropbox\n\nOther Information\n\nHow did you hear about this position?\n\nYour Legal Work Authorization in the US?\n\nAre you currently employed?\n\nWill you be able to join us on our W-2?\n\nWhat is your desired salary / hourly rate?\n\nIf on a Visa, will you be able to transfer your Work Visa to us?\n\nWhat is your motivation for Change/New Job Opportunity?\n\nIf Currently working, what is your Notice period?\n\nWhat is your current location?\n\nAre you ready to relocate?\n\nCan you provide proof of legal right to work in the United States?\n\nif Hired when will you be able to start?\n\n#J-18808-Ljbffr","company":"Cedent","rawCompany":"cedent","city":"Largo","state":"FL","isRemote":false,"isActive":false,"createdAt":"2026-09-02T04:01:02.024Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2041.00","title":"Chemical Engineers","slug":"chemical-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"},{"code":"325611","title":"Soap and Other Detergent Manufacturing","slug":"soap-and-other-detergent-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer (Largo, FL)","description":"Primary Purpose\nProvide engineering services for full product life cycle including process robustness review, process optimization initiatives, product equipment transfers, process validations, cleaning validations, material changes, and commercial product manufacturing technical support.\n\nMajor Duties and Responsibilities\n\nIndependent management of product transfers, performing equipment fit and gap analyses, and authoring critical documentation such as Risk Assessment, OOS Investigation, Process Validation protocols, Cleaning Validation protocols, etc.\n\nFocused on process optimization in all phases of manufacturing process (blending, filling, packaging, etc) using lean or six sigma tools for optimal impact.\n\nLead and/or support cleaning validation and process validation efforts and projects, as needed to support commercial operations.\n\nIdentify and lead continuous improvement engineering projects to enhance process robustness, manufacturing efficiency, and deviation reduction through engineering controls.\n\nGenerate technical reports, specifications, and other supporting documentation as needed.\n\nCoordinate with outside vendors, contract labs, and equipment manufacturers as needed to support project or related work deliverables.\n\nProvide day-to-day technical support for commercial manufacturing. Conduct technical investigations, write reports, and aid in the close-out of deviations.\n\nSupport business with strategic analysis and proactive concept development for manufacturing process optimization projects.\n\nCollaborates across various departments like Manufacturing, Quality, R&D teams, Engineering, and Project Management to ensure project success.\n\nGenerate/maintain documents and provide related technical support related to GMP Manufacturing executions, product impact assessments and periodic reviews.\n\nParticipate in the project team meetings, decisions, and creation of milestones representing process engineering.\n\nProcess training, as needed, in adherence to company policies and quality requirements.\n\nEvaluate, define, and provide user requirements for process equipment associated with drug product manufacturing.\n\nPrepare and present data associated with manufacturing processes to internal and external teams as required.\n\nKeep current on regulatory and quality requirements for manufacturing, including FDA-regulated products and cGMP compliance.\n\nInteracts regularly with senior technical peers and colleagues.\n\nOther functions as required to support existing operations and client-driven projects.\n\nManufacturing, Science and Technology\n\nQualifications\n\nBachelor’s degree in chemical engineering or relevant experience (MS Preferred)\n\nAt least 5-10 years of process engineering/technical services/MS&T experience in the pharmaceutical/chemical manufacturing industry, preferably with cGMP manufacturing of FDA-regulated drug products.\n\nCritical Skills and Abilities\n\nDemonstrated ability for independent work, thought, and analysis.\n\nAbility to coordinate with internal groups as needed to achieve desired goals and deliverables (Manufacturing, Engineering, Supply chain, QA, QC, R&D, Project Management, etc.).\n\nExceptional time management and multi-tasking skills.\n\nExcellent written and verbal communication skills with expertise in good documentation practices.\n\nAbility to perform statistical analysis of data and interpretation of data.\n\nMust be able to work extended hours on evening and weekends as required.\n\nMust be capable of detailed recordkeeping and communicating results to others.\n\nExperience with pharmaceutical and consumer products related to creams, lotions, liquids, aerosols, nasal sprays, and/or gels is a plus.\n\nCleaning validation experience is strongly preferred.\n\nProcess validation experience is strongly preferred.\n\nComputer Skills\n\nProficient with Microsoft Office 365, including Teams, Word, Excel, and PowerPoint.\n\nMinitab experience is preferred but not required.\n\nPhysical Demands\n\nMust be able to lift and maneuver forty pounds.\n\nMust be capable of standing for extended periods of time.\n\nMust be able to wear personal protection equipment which includes gloves and respirator when required.\n\nAbility to perform work in a manufacturing environment where there is exposure to occupational hazards.\n\nMust be able to work extended hours on evenings and weekends as required.\n\nPersonal Information\n\nFirst name\n\nLast name\n\nEmail\n\nAddress\n\nCity\n\nState\n\nZip code\n\nPhone number\n\nAttachments\n\nAttach your Resume\n\nAttach Dropbox\n\nPaste Attach a Cover letter\n\nAttach Dropbox\n\nOther Information\n\nHow did you hear about this position?\n\nYour Legal Work Authorization in the US?\n\nAre you currently employed?\n\nWill you be able to join us on our W-2?\n\nWhat is your desired salary / hourly rate?\n\nIf on a Visa, will you be able to transfer your Work Visa to us?\n\nWhat is your motivation for Change/New Job Opportunity?\n\nIf Currently working, what is your Notice period?\n\nWhat is your current location?\n\nAre you ready to relocate?\n\nCan you provide proof of legal right to work in the United States?\n\nif Hired when will you be able to start?\n\n#J-18808-Ljbffr","datePosted":"2026-09-02T04:01:02.024Z","dateModified":"2026-09-02T04:01:02.024Z","hiringOrganization":{"@type":"Organization","name":"Cedent","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Largo","addressRegion":"FL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"ebddb61035a69952596db44c"},"url":"https://jobsearcher.com/jobs/ebddb61035a69952596db44c"}}