System Administrator and Validation Lead (GxP systems)

Foster City, CA, US • Posted 2 hours ago • Updated 2 hours ago
Contract Independent
Contract Corp To Corp
Contract W2
No Travel Required
On-site
Depends on Experience
Fitment

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Job Details

Skills

  • Auditing
  • Change Control
  • Collaboration
  • Communication
  • Computerized System Validation
  • Corrective And Preventive Action
  • Data Integrity
  • Data Link Layer
  • GxP
  • Life Sciences
  • Management
  • Physical Layer
  • QMS
  • Quality Control
  • Regulatory Compliance
  • Reliability Engineering
  • Status Reports
  • System Administration
  • Tableau
  • Testing
  • Training
  • Veeva

Summary

Role: System Administrator and Validation Lead (GxP systems)

Location: Foster City, CA

Job Summary

We are seeking a highly skilled and experienced System Administrator and Validation Lead to support GxP systems within a life sciences environment. This role combines system administration, validation engineering, and operational support responsibilities to ensure system reliability, compliance, and performance.

The ideal candidate will have strong expertise in GxP systems, validation processes, and infrastructure management, and will collaborate across teams to ensure smooth operations, deliver training, and drive continuous improvements.

Key Responsibilities

System Administration & Operational Support
• Provide L1 and L2 support for GxP applications, ensuring timely resolution of incidents and requests
• Execute and monitor scheduled jobs to maintain uninterrupted system operations
• Manage user access and license administration (e.g., Tableau, application access)
• Generate and maintain system performance and status reports
• Coordinate priorities across the Global Quality Control organization
• Maintain continuous communication with system managers, stakeholders, and technical teams

Validation & Compliance
• Author, review, and execute validation protocols (CSV lifecycle) in both paper-based and ValGenesis systems
• Perform and support validation testing activities to ensure audit readiness
• Create and manage quality event records (Change Control, Deviations, CAPA) in Veeva QMS
• Ensure adherence to GxP, regulatory, and data integrity requirements

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91081606
  • Position Id: 8968367
  • Posted 2 hours ago
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