{"schemaVersion":"jobsearcher.job.v1","id":"b8b58fb4c06e2a7db6e9d7a3","url":"https://jobsearcher.com/jobs/b8b58fb4c06e2a7db6e9d7a3","canonicalUrl":"https://jobsearcher.com/jobs/b8b58fb4c06e2a7db6e9d7a3","title":"Computer Systems Validation (CSV) IT Engineer (IT Support Specialist)","description":"Job Category: Information Technology\r\nWork Location: On-Site\r\nOffice Location: Tucker, GA, US\r\nJob Type: Full Time\r\nJob ID: 6111\r\nAt Corbion, we exist to champion preservation in all its forms, preserving food and food production, health, and our planet.\r\nThe CSV IT Engineer is responsible for ensuring that computerized systems used in Corbion-regulated environments comply with applicable Good Manufacturing Practice (GMP) regulations, data integrity standards, and validation requirements. In this role, you will support the validation lifecycle of GxP systems, including infrastructure, applications, cloud environments, manufacturing systems, laboratory systems, and quality systems.\r\nYou will be a part of the global Corbion IT organization as a full-time onsite position, based in Tucker, Georgia. Works closely with Regional & Global IT, Quality Assurance (QA), Manufacturing, Engineering, Automation, and business stakeholders to ensure systems are implemented, maintained, and operated in compliance with FDA and other Corbion regulatory expectations.\r\nThis position is critical in maintaining validated states for computerized systems and ensuring compliance with regulations of: 21 CFR Part 11, GAMP 5, ALCOA+ Data Integrity principles, FDA GMP requirements, Corbion Service Management SLA and quality standards.\r\nKey Responsibilities\r\nProvide daily IT operations support, including end-user support, desktop deployments, service management activities, and general IT support across Company locations.\r\nLead and execute the full Computer System Validation (CSV) lifecycle for GxP-regulated computerized systems, ensuring systems remain in a validated state through implementation, operation, maintenance, periodic review, and retirement.\r\nDevelop, execute, and maintain validation documentation, including validation plans, risk assessments, traceability matrices, test protocols/scripts, validation summary reports, and validation records.\r\nValidate and support regulated systems, including SCADA/HMI systems, historian platforms, laboratory systems (LIMS), cloud-based GxP applications, and related infrastructure.\r\nEnsure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles, GMP requirements, and Company quality standards.\r\nPerform risk assessments using GAMP 5 methodologies and evaluate system security, audit trails, electronic signatures, user access controls, and data integrity controls.\r\nManage validation impacts associated with system changes, including change controls, regression testing, requalification activities, deviations, CAPAs, and remediation efforts.\r\nCoordinate validation activities and deliverables with vendors, third-party integrators, and internal stakeholders.\r\nSupport regulatory inspections, customer audits, and internal compliance reviews, including addressing audit findings and implementing corrective actions.\r\nSupport disaster recovery, backup validation, and business continuity testing to ensure compliance and operational readiness.\r\nPartner with Quality Assurance, Manufacturing, Engineering, Automation, Infrastructure, Cybersecurity, and business teams to ensure compliant system implementation and operation.\r\nProvide compliance and validation guidance during system implementations, upgrades, and enhancements.\r\nTrain end users on validated procedures, compliance requirements, and data integrity expectations.\r\nMonitor GMP systems, backups, and data integrity controls while supporting ongoing system maintenance, upgrades, and continuous improvement initiatives.\r\nRequired Qualifications\r\nAssociate's degree in Computer Science, Engineering, Biotechnology, Pharmaceutical Sciences, Automation Engineering, or related discipline.\r\n5+ years in IT Infrastructure and pharmaceutical, biotechnology, medical device, or regulated healthcare environments.\r\nExtensive experience and proven track record of CSV lifecycle management, GMP environments, and regulatory audits.\r\nTechnical Skills Validation & Compliance: GAMP 5, FDA 21 CFR Part 11, Annex 11, and Data Integrity principles.\r\nIT & Infrastructure experience: VMware, Veeam Backups and Replication, Microsoft End User Computing, Windows Server, Active Directory, SQL/Postgres databases, Cloud technologies, and Cisco LAN and Wireless proven skills.\r\nPreferred Certifications: VMware VCP-DCV + VCP-VCF, Veeam Certified Engineer VMCE, Microsoft MCP, ITIL, Cisco LAN and WLAN technologies, and ISPE GAMP Certification.\r\nExcellent technical writing and detail-oriented mindset.\r\nAnalytical problem-solving.\r\nExceptional communication skills.\r\nExcellent time management and prioritization.\r\nOur Offer\r\nThe anticipated compensation range for this position is $96,000 to $115,000. The final pay offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and years of experience within the job, the type, years of and experience within the industry, education, etc. Please note, Corbion is a multi-state employer and this pay scale may not reflect positions that work in other states or locations.\r\nPaid time off, including company holidays\r\n401K with company match\r\nMedical, dental, vision and basic life insurance coverage are offered to employees and eligible dependents (provided they meet eligibility requirements)\r\nFlexible spending accounts\r\nEducation assistance\r\nShort- and long-term disability\r\nEmployee Assistance Program (EAP)\r\nLifestyle and wellness benefits\r\n*Please note, this is intended to provide a general description of benefits and other compensation and is not a substitute for applicable plan documents or company policies. Eligibility requirements for these benefits will be controlled by applicable plan documents.\r\nCorbion is an equal opportunity employer and committed to a diverse workplace. All applicants will be considered equally without regard to race, color, ethnicity, veteran status, religion, national origin, marital status, political affiliation, age, sex, sexual orientation, handicapping condition, membership in an organization or any other non-merit factors.\r\nCorbion provides reasonable accommodation to applicants.\r\nEOE/M/F/Vet/Disabled\r\nJ-18808-Ljbffr","company":"Corbion","rawCompany":"corbion","city":"Tucker","state":"GA","isRemote":false,"isActive":false,"createdAt":"2026-07-16T01:42:04.559Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"15-1299.08","title":"Computer Systems Engineers/Architects","slug":"computer-systems-engineers-architects"},{"code":"15-1211.00","title":"Computer Systems Analysts","slug":"computer-systems-analysts"}],"industries":[{"code":"541512","title":"Computer Systems Design Services","slug":"computer-systems-design-services"},{"code":"541519","title":"Other Computer Related Services","slug":"other-computer-related-services"},{"code":"541513","title":"Computer Facilities Management Services","slug":"computer-facilities-management-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Computer Systems Validation (CSV) IT Engineer (IT Support Specialist)","description":"Job Category: Information Technology\r\nWork Location: On-Site\r\nOffice Location: Tucker, GA, US\r\nJob Type: Full Time\r\nJob ID: 6111\r\nAt Corbion, we exist to champion preservation in all its forms, preserving food and food production, health, and our planet.\r\nThe CSV IT Engineer is responsible for ensuring that computerized systems used in Corbion-regulated environments comply with applicable Good Manufacturing Practice (GMP) regulations, data integrity standards, and validation requirements. In this role, you will support the validation lifecycle of GxP systems, including infrastructure, applications, cloud environments, manufacturing systems, laboratory systems, and quality systems.\r\nYou will be a part of the global Corbion IT organization as a full-time onsite position, based in Tucker, Georgia. Works closely with Regional & Global IT, Quality Assurance (QA), Manufacturing, Engineering, Automation, and business stakeholders to ensure systems are implemented, maintained, and operated in compliance with FDA and other Corbion regulatory expectations.\r\nThis position is critical in maintaining validated states for computerized systems and ensuring compliance with regulations of: 21 CFR Part 11, GAMP 5, ALCOA+ Data Integrity principles, FDA GMP requirements, Corbion Service Management SLA and quality standards.\r\nKey Responsibilities\r\nProvide daily IT operations support, including end-user support, desktop deployments, service management activities, and general IT support across Company locations.\r\nLead and execute the full Computer System Validation (CSV) lifecycle for GxP-regulated computerized systems, ensuring systems remain in a validated state through implementation, operation, maintenance, periodic review, and retirement.\r\nDevelop, execute, and maintain validation documentation, including validation plans, risk assessments, traceability matrices, test protocols/scripts, validation summary reports, and validation records.\r\nValidate and support regulated systems, including SCADA/HMI systems, historian platforms, laboratory systems (LIMS), cloud-based GxP applications, and related infrastructure.\r\nEnsure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles, GMP requirements, and Company quality standards.\r\nPerform risk assessments using GAMP 5 methodologies and evaluate system security, audit trails, electronic signatures, user access controls, and data integrity controls.\r\nManage validation impacts associated with system changes, including change controls, regression testing, requalification activities, deviations, CAPAs, and remediation efforts.\r\nCoordinate validation activities and deliverables with vendors, third-party integrators, and internal stakeholders.\r\nSupport regulatory inspections, customer audits, and internal compliance reviews, including addressing audit findings and implementing corrective actions.\r\nSupport disaster recovery, backup validation, and business continuity testing to ensure compliance and operational readiness.\r\nPartner with Quality Assurance, Manufacturing, Engineering, Automation, Infrastructure, Cybersecurity, and business teams to ensure compliant system implementation and operation.\r\nProvide compliance and validation guidance during system implementations, upgrades, and enhancements.\r\nTrain end users on validated procedures, compliance requirements, and data integrity expectations.\r\nMonitor GMP systems, backups, and data integrity controls while supporting ongoing system maintenance, upgrades, and continuous improvement initiatives.\r\nRequired Qualifications\r\nAssociate's degree in Computer Science, Engineering, Biotechnology, Pharmaceutical Sciences, Automation Engineering, or related discipline.\r\n5+ years in IT Infrastructure and pharmaceutical, biotechnology, medical device, or regulated healthcare environments.\r\nExtensive experience and proven track record of CSV lifecycle management, GMP environments, and regulatory audits.\r\nTechnical Skills Validation & Compliance: GAMP 5, FDA 21 CFR Part 11, Annex 11, and Data Integrity principles.\r\nIT & Infrastructure experience: VMware, Veeam Backups and Replication, Microsoft End User Computing, Windows Server, Active Directory, SQL/Postgres databases, Cloud technologies, and Cisco LAN and Wireless proven skills.\r\nPreferred Certifications: VMware VCP-DCV + VCP-VCF, Veeam Certified Engineer VMCE, Microsoft MCP, ITIL, Cisco LAN and WLAN technologies, and ISPE GAMP Certification.\r\nExcellent technical writing and detail-oriented mindset.\r\nAnalytical problem-solving.\r\nExceptional communication skills.\r\nExcellent time management and prioritization.\r\nOur Offer\r\nThe anticipated compensation range for this position is $96,000 to $115,000. The final pay offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and years of experience within the job, the type, years of and experience within the industry, education, etc. Please note, Corbion is a multi-state employer and this pay scale may not reflect positions that work in other states or locations.\r\nPaid time off, including company holidays\r\n401K with company match\r\nMedical, dental, vision and basic life insurance coverage are offered to employees and eligible dependents (provided they meet eligibility requirements)\r\nFlexible spending accounts\r\nEducation assistance\r\nShort- and long-term disability\r\nEmployee Assistance Program (EAP)\r\nLifestyle and wellness benefits\r\n*Please note, this is intended to provide a general description of benefits and other compensation and is not a substitute for applicable plan documents or company policies. Eligibility requirements for these benefits will be controlled by applicable plan documents.\r\nCorbion is an equal opportunity employer and committed to a diverse workplace. All applicants will be considered equally without regard to race, color, ethnicity, veteran status, religion, national origin, marital status, political affiliation, age, sex, sexual orientation, handicapping condition, membership in an organization or any other non-merit factors.\r\nCorbion provides reasonable accommodation to applicants.\r\nEOE/M/F/Vet/Disabled\r\nJ-18808-Ljbffr","datePosted":"2026-07-16T01:42:04.559Z","dateModified":"2026-07-16T01:42:04.559Z","hiringOrganization":{"@type":"Organization","name":"Corbion","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Tucker","addressRegion":"GA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"b8b58fb4c06e2a7db6e9d7a3"},"url":"https://jobsearcher.com/jobs/b8b58fb4c06e2a7db6e9d7a3"}}