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# Empower System Administrator

- **Company:** Insight Global
- **Location:** Cumnock, NC, United States
- **Contract:** Permanent contract
- **Skills:** Data Integrity, Data Systems, Document Management Systems, Connectivity Problems
- **Published:** October 9, 2026
- **Apply:** https://www.disabledperson.com/jobs/75951223-empower-system-administrator

## About the Role

This is an excellent opportunity for either an experienced Empower Administrator or a laboratory professional with strong Empower expertise looking to transition into a systems-focused role., * Experience working in a GMP-regulated pharmaceutical, biotechnology, or life sciences environment

 * Hands-on experience with Waters Empower CDS
 * Strong understanding of GMP documentation practices and controlled document management
 * Experience troubleshooting Empower systems and chromatography-related laboratory instrumentation
 * Knowledge of laboratory workflows and analytical testing environments
 * Background supporting HPLC and UPLC systems
 * Familiarity with chromatography laboratory operations
 * Knowledge of 21 CFR Part 11 requirements and electronic data compliance
 * Understanding of GMP data integrity principles

## Description

We are seeking an Empower Systems Administrator to support a growing GMP-regulated laboratory environment. This individual will serve as a key resource responsible for Empower administration, chromatography system support, GMP documentation management, troubleshooting laboratory systems, and ensuring compliance with regulatory and quality requirements., * Administer and support the Waters Empower Chromatography Data System (CDS) within a GMP-regulated environment

 * Troubleshoot Empower-related issues, instrument connectivity problems, and user support requests
 * Support chromatographic instrumentation including HPLC, UPLC, electrophoresis systems, and other Empower-connected laboratory equipment
 * Author, revise, and maintain GMP documentation, including SOPs, work instructions, job aids, and system administration procedures
 * Collaborate with laboratory, quality, and technical teams to ensure systems remain compliant and operational
 * Support instrument lifecycle management activities and release of systems into GMP environments
 * Assist with change control, data integrity, and compliance-related assessments
 * Investigate system issues and recommend corrective actions
 * Participate in daily operational meetings and support ongoing laboratory initiatives
 * Ensure documentation and practices align with current regulatory requirements and internal quality standards