Empower System Administrator

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

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