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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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