{"schemaVersion":"jobsearcher.job.v1","id":"0543375fd3213aa1c5d80e27","url":"https://jobsearcher.com/jobs/0543375fd3213aa1c5d80e27","canonicalUrl":"https://jobsearcher.com/jobs/0543375fd3213aa1c5d80e27","title":"Process Engineer","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\n\nWe are seeking an experienced Process Engineer to provide technical engineering support within a regulated pharmaceutical/biotechnology manufacturing environment. The Process Engineer will work closely with Engineering, Manufacturing, Quality, Validation, Maintenance, and other cross-functional teams to support process performance, equipment and system improvements, troubleshooting, capital projects, and continuous improvement initiatives. The ideal candidate is a hands-on engineer with strong technical problem-solving skills, experience working in GMP-regulated manufacturing environments, and the ability to independently manage engineering activities from problem identification through implementation and closure.\n\nDescription:\n\nProvide day-to-day process engineering support to manufacturing and engineering operations.\nEvaluate process performance and identify opportunities to improve reliability, efficiency, capacity, quality, and operational performance.\nLead or support troubleshooting and root-cause investigations related to manufacturing processes, equipment, and systems.\nDevelop and implement engineering solutions to address process and equipment issues.\nSupport capital projects, equipment upgrades, system modifications, and process improvement initiatives.\nDevelop and review technical documentation including engineering assessments, specifications, protocols, reports, procedures, and change-control documentation.\nSupport equipment and process design reviews, technical evaluations, and implementation activities.\nCoordinate engineering activities with Manufacturing, Quality, Validation, Automation, Maintenance, and other technical groups.\nSupport commissioning, qualification, validation, startup, and turnover activities as required.\nParticipate in change controls, deviations, investigations, CAPAs, and risk assessments from an engineering perspective.\nAnalyze process and equipment data to identify trends, recurring issues, and improvement opportunities.\nProvide technical recommendations and support the development of corrective and preventive solutions.\nCoordinate activities with vendors, contractors, and equipment suppliers when required.\nEnsure engineering activities are performed in accordance with applicable GMP requirements, engineering standards, procedures, and safety expectations.\nMaintain clear documentation and communicate project status, technical issues, risks, and recommendations to stakeholders.\nSupport continuous improvement and standardization initiatives within the Engineering organization.\n\nQualifications:\n\nBachelor’s degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, Bioengineering, or a related engineering discipline.\nRelevant process engineering experience within the pharmaceutical, biotechnology, medical device, or regulated manufacturing industry.\nStrong understanding of manufacturing processes, equipment, utilities, and engineering principles.\nExperience troubleshooting process and equipment-related issues in a manufacturing environment.\nKnowledge of GMP requirements, change control, deviations, CAPA, and engineering documentation practices.\nExperience supporting equipment modifications, process improvements, or capital projects.\nAbility to analyze technical data and translate findings into practical engineering solutions.\nStrong technical writing, documentation, and communication skills.\nDemonstrated ability to work independently while collaborating effectively with multidisciplinary teams.\nStrong organizational skills with the ability to manage multiple activities and priorities.\n5+ years of relevant process or manufacturing engineering experience within the pharmaceutical or biotechnology industry.\nExperience supporting biopharmaceutical manufacturing processes and equipment.\nExperience with commissioning, qualification, validation, and equipment startup.\nFamiliarity with process optimization, process characterization, troubleshooting methodologies, and root-cause analysis.\nExperience supporting capital projects and equipment/system lifecycle activities.\nWorking knowledge of automation and process control systems.\nExperience working in a highly regulated GMP manufacturing environment.\n\nKey Competencies: Process Engineering | Manufacturing Support | Troubleshooting | Root Cause Analysis | Process Optimization | Equipment & Systems | Technical Documentation | Change Control | CAPA | GMP Compliance | Capital Projects | CQV Support | Cross-Functional Collaboration | Continuous Improvement\n\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\n\nExcited to build something meaningful together? We look forward to hearing from you.\n\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","company":"Validation","rawCompany":"validation","city":"Durham","state":"NC","isRemote":false,"isActive":false,"createdAt":"2026-10-16T09:52:43.615Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\n\nWe are seeking an experienced Process Engineer to provide technical engineering support within a regulated pharmaceutical/biotechnology manufacturing environment. The Process Engineer will work closely with Engineering, Manufacturing, Quality, Validation, Maintenance, and other cross-functional teams to support process performance, equipment and system improvements, troubleshooting, capital projects, and continuous improvement initiatives. The ideal candidate is a hands-on engineer with strong technical problem-solving skills, experience working in GMP-regulated manufacturing environments, and the ability to independently manage engineering activities from problem identification through implementation and closure.\n\nDescription:\n\nProvide day-to-day process engineering support to manufacturing and engineering operations.\nEvaluate process performance and identify opportunities to improve reliability, efficiency, capacity, quality, and operational performance.\nLead or support troubleshooting and root-cause investigations related to manufacturing processes, equipment, and systems.\nDevelop and implement engineering solutions to address process and equipment issues.\nSupport capital projects, equipment upgrades, system modifications, and process improvement initiatives.\nDevelop and review technical documentation including engineering assessments, specifications, protocols, reports, procedures, and change-control documentation.\nSupport equipment and process design reviews, technical evaluations, and implementation activities.\nCoordinate engineering activities with Manufacturing, Quality, Validation, Automation, Maintenance, and other technical groups.\nSupport commissioning, qualification, validation, startup, and turnover activities as required.\nParticipate in change controls, deviations, investigations, CAPAs, and risk assessments from an engineering perspective.\nAnalyze process and equipment data to identify trends, recurring issues, and improvement opportunities.\nProvide technical recommendations and support the development of corrective and preventive solutions.\nCoordinate activities with vendors, contractors, and equipment suppliers when required.\nEnsure engineering activities are performed in accordance with applicable GMP requirements, engineering standards, procedures, and safety expectations.\nMaintain clear documentation and communicate project status, technical issues, risks, and recommendations to stakeholders.\nSupport continuous improvement and standardization initiatives within the Engineering organization.\n\nQualifications:\n\nBachelor’s degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, Bioengineering, or a related engineering discipline.\nRelevant process engineering experience within the pharmaceutical, biotechnology, medical device, or regulated manufacturing industry.\nStrong understanding of manufacturing processes, equipment, utilities, and engineering principles.\nExperience troubleshooting process and equipment-related issues in a manufacturing environment.\nKnowledge of GMP requirements, change control, deviations, CAPA, and engineering documentation practices.\nExperience supporting equipment modifications, process improvements, or capital projects.\nAbility to analyze technical data and translate findings into practical engineering solutions.\nStrong technical writing, documentation, and communication skills.\nDemonstrated ability to work independently while collaborating effectively with multidisciplinary teams.\nStrong organizational skills with the ability to manage multiple activities and priorities.\n5+ years of relevant process or manufacturing engineering experience within the pharmaceutical or biotechnology industry.\nExperience supporting biopharmaceutical manufacturing processes and equipment.\nExperience with commissioning, qualification, validation, and equipment startup.\nFamiliarity with process optimization, process characterization, troubleshooting methodologies, and root-cause analysis.\nExperience supporting capital projects and equipment/system lifecycle activities.\nWorking knowledge of automation and process control systems.\nExperience working in a highly regulated GMP manufacturing environment.\n\nKey Competencies: Process Engineering | Manufacturing Support | Troubleshooting | Root Cause Analysis | Process Optimization | Equipment & Systems | Technical Documentation | Change Control | CAPA | GMP Compliance | Capital Projects | CQV Support | Cross-Functional Collaboration | Continuous Improvement\n\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\n\nExcited to build something meaningful together? We look forward to hearing from you.\n\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","datePosted":"2026-10-16T09:52:43.615Z","dateModified":"2026-10-16T09:52:43.615Z","hiringOrganization":{"@type":"Organization","name":"Validation","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Durham","addressRegion":"NC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"0543375fd3213aa1c5d80e27"},"url":"https://jobsearcher.com/jobs/0543375fd3213aa1c5d80e27"}}