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IT SysAdmin

Full-time

Insight Global

Bachelor's degree in Life Sciences, Chemistry, Biology, Engineering, Computer Science, or a related field

  • 3+ years of experience administering Waters Empower CDS
  • Experience supporting GMP-regulated pharmaceutical, biotechnology, or medical device laboratories
  • Understanding of chromatography systems including HPLC and UPLC platforms
  • Experience with computerized system validation and data integrity requirements
  • Experience with change controls, investigations, CAPAs, and quality systems documentation
  • Empower certification or advanced Empower administration training

Experience supporting multiple laboratory informatics platforms such as LIMS, ELN, or SDMS
Experience with Active Directory, user account management, and networked laboratory systems
Experience supporting commercial pharmaceutical manufacturing operations

We are seeking an experienced Empower System Administrator to support laboratory operations within a highly regulated pharmaceutical manufacturing environment. This individual will serve as the subject matter expert for the Waters Empower Chromatography Data System (CDS), partnering with Quality Control, Quality Assurance, Laboratory Operations, Validation, and IT teams to ensure system performance, compliance, and data integrity.
The ideal candidate brings a combination of Empower administration expertise, GMP laboratory experience, and a strong understanding of computerized systems used in pharmaceutical testing environments.
Serve as the primary administrator for the Waters Empower Chromatography Data System (CDS)
Manage user accounts, permissions, security settings, and system configuration within Empower
Support software upgrades, patches, system maintenance, and lifecycle management activities
Support computerized system validation activities, including qualification, testing, and documentation
Support data integrity initiatives and ensure compliance with GMP, FDA, and global regulatory requirements
Collaborate with IT, automation, validation, and laboratory teams during system implementations and enhancements
Generate reports, queries, and system metrics to support business and quality objectives
Participate in internal and regulatory inspections as the CDS subject matter expert

Vacancy posted 2 days ago
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