
Empower System Administrator
Sanford, NCJobSeen 4 days agoSeen in employer's feed 4 days ago
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Job overview
The Empower Systems Administrator will support a growing GMP-regulated laboratory environment, administering Waters Empower CDS and supporting chromatography systems. The role is suited to an experienced Empower administrator or a laboratory professional with strong Empower expertise seeking a systems-focused position. It includes troubleshooting, documentation management, instrument lifecycle support, and work with laboratory, quality, and technical teams to maintain regulatory and quality compliance.
Skills & qualifications
Skills
Qualifications
Full job description
Job 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. 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. Responsibilities 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
Skills and Requirements
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
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [email protected].
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