水平: Mid-Senior level

工作类型: Contract

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工作内容

Roles and Responsibilities

  • 4+ years’ Experience in Validating GxP applications.
  • Validation Capacity planning
  • Validation operational management
  • Team management
  • Knowledge management
  • Experience in Pharma R&D Clinical systems like CTMS, Lab, CDMS, EDC, Veeva Vault, QMS and Safety Systems
  • Experience in FDA and/or Global regulated environment with good understanding of GCP , GLP and Risk based validation strategy
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最后期限: 02-01-2026

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