GxP Laboratory Systems Administrator

Role: GxP Laboratory Systems Administrator supporting laboratory systems across Manufacturing, CMC, QC, BioAnalytical, DMPK, Clinical Pharmacology, and BioMarkers. Responsibilities include system administration, configuration, validation, deployment, troubleshooting, and supporting GxP-compliant laboratory applications, with a focus on ensuring compliance and smooth operation. The role involves collaborating with business units, internal IS&I teams, and vendors, managing user access, and contributing to audit and validation documentation. Qualifications: Bachelor's in computer science, life sciences, or related; 4+ years experience with Laboratory Information Management Systems (LIMS), Chromatography Data Systems, and laboratory support systems in GxP environments; strong knowledge of computer programs like MS Office and data systems; ability to multitask under tight deadlines. Preferred: extensive validation experience with Agilent systems, familiarity with pharma/CRO regulations (GxP, 21 CFR Part 11, EU Annex 11), asset management, and project management certification. HighValue: GxP laboratory systems, validation, GxP compliance, regulated environment, pharma/CRO experience, validation documentation, cross-departmental collaboration. Location: Wisconsin; salary range $90,000-$115,000 USD.