GxP Lab IT Administrator - Onsite, Compliance & Support

Inherent Technologies, Inc.; Wilmington (OH); On-site; USD 65,000 - 90,000; Full time

Job summary

Inherent Technologies, Inc. in Wilmington, OH is seeking a Lab Support IT Administrator to manage Windows-based lab workstations and the supporting infrastructure onsite.

You will handle provisioning, imaging, deployments, upgrades, and validation support, while minimizing downtime and ensuring data integrity in a GMP/GxP setting. The role emphasizes CSV compliance, FDA 21 CFR Part 11 alignment, and collaboration with validation teams, vendors, and lab personnel to maintain validated, auditable

Qualifications

• Experience administering Windows-based laboratory IT environments.
• Familiarity with GMP/GLP/GxP regulatory requirements.
• Experience supporting validation activities and CSV methodologies.
• Ability to manage lifecycle activities (provisioning, imaging, deployment, upgrades).
• Knowledge of risk assessments and investigations (RCA, FMEA).
• Experience with Active Directory, GPOs, and access management.

Responsibilities

• Administer, support, maintain Windows lab workstations and related infrastructure.
• Install, configure, patch, and maintain operating systems and instrument software.
• Manage lifecycle activities: provisioning, imaging, deployment, upgrades, migrations, validation, decommissioning.
• Troubleshoot hardware/software to minimize downtime on lab instruments.
• Coordinate upgrades, software releases, and system enhancements with lab staff and vendors.
• Support data integrity, validation, and regulatory inspections.

Skills

Windows OS administration

Active Directory

GxP compliance

CSV/Validation

Risk assessment

Root cause analysis

IT infrastructure

Tools

AD tooling

Job description

Inherent Technologies, Inc. in Wilmington, OH is seeking a Lab Support IT Administrator to manage Windows-based lab workstations and the supporting infrastructure onsite.

You will handle provisioning, imaging, deployments, upgrades, and validation support, while minimizing downtime and ensuring data integrity in a GMP/GxP setting. The role emphasizes CSV compliance, FDA 21 CFR Part 11 alignment, and collaboration with validation teams, vendors, and lab personnel to maintain validated, auditable