SPECS

60 Spec System Administrator Jobs Hiring Near You

Create and maintain technical documentation, including design specs and test plans Requirements ... ServiceNow Certified System Administrator (CSA) or Certified Application Developer (CAD) preferred

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Develop, maintain, and administer piping catalogs and specifications within the project's 3D design ... or equivalent 3D design systems. * Develop and implement best practices for catalog and ...

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Develop, maintain, and administer piping catalogs and specifications within the project's 3D design ... or equivalent 3D design systems. * Develop and implement best practices for catalog and ...

... functional specs. * Configuration Design - Design HRSD applications (Configurable Workspace ... ServiceNow Certified System Administrator (CSA) or Certified Implementation Specialist (CIS) - HRSD ...

The Job entails Product Information System Salsify (PIM) implementation * Normalize and validate ... Conduct regular content audits to ensure content is correct and adheres to specs and policies ...

$77K - $94K/yr

Act as the primary system administrator for Oracle ERP Cloud/NetSuite: user provisioning, role and ... leaders and writing functional specs for technical teams * Excellent written and verbal ...

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Develop, maintain, and administer piping catalogs and specifications within the project's 3D design ... or equivalent 3D design systems. * Develop and implement best practices for catalog and ...

Be Seen First

Develop, maintain, and administer piping catalogs and specifications within the project's 3D design ... or equivalent 3D design systems. * Develop and implement best practices for catalog and ...

Showing results 21-40

GxP Laboratory Systems Administrator

Madison, WI โ€ข On-site

Scorpion Therapeutics
51 - 200 employees

Other

Posted 11 days ago


Job description

Responsibilities
Business:

  • Support and system administration for identified applications

  • Investigate and resolve technical and business process issues

  • Communicate issues/resolutions with users and department managers

  • Escalate issues to application vendors as necessary

  • Troubleshoot and collaborate with end users and departmental managers

  • Maintain functional subject matter knowledge for assigned applications

  • Perform other duties as assigned


Regulatory:

  • Perform periodic application review and manage user access

  • Represent application documentation in client and regulatory audits

  • Contribute to audit finding responses

  • Contribute to CSV/CSA/computer system validation and software assurance projects, including application change control as required by GxP, policies, and SDLC

  • Draft CSV/CSA documentation (validation plans, design specs, traceability matrices, user requirements, test scripts, deviations, summary reports)


Information Systems/Informatics:

  • Coordinate communication between business and IS/Informatics

  • Triage escalation of technical issues

  • Update global systems inventory for applications

  • Coordinate releases into Development, Testing, and Production environments

  • Develop business scenarios to test applications

  • Verify installation and operation

  • Document analysis/testing for infrastructure changes (e.g., OS patches, major network changes)


Requirements

  • Bachelorโ€™s in CS or life sciences (or related field) or equivalent experience

  • 4+ years administering/operating/maintaining LIMS, chromatography data systems, spectrophotometry systems, and related lab systems in a GxP environment

  • Advanced knowledge of computer programs (e.g., MS Word/Excel, data acquisition systems)

  • Ability to multi-task across projects and initiatives

  • Ability to deliver high-quality results under strict deadlines

  • Ability to work independently and with others


Preferred

  • Experience validating/supporting Agilent systems (Openlab, Chemstation, Cary UV)

  • Knowledge of GxP/CSV-CSA/21 CFR Part 11/EU Annex 11/SDLC

  • Experience with regulated asset management and environment monitor applications

  • Computer System Validation and GxP (21 CFR Part 11, Annex 11)

  • Pharmaceutical or CRO experience

  • Project Management certification


Benefits (if part of description)

  • Competitive salaries and an excellent benefit package

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