Supply Chain Analyst - GSK0JP00106870
- Ware, Hertfordshire
- Temporary
- Full-time
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- Effectively execute pre-production activities to enable on-time job handover within Global Packaging Operations.
- Timely progression and approval of clinical site temperature excursions to ensure continuity of clinical supplies.
- Providing support to the Global Packaging Operations and Clinical Interface teams within the Clinical Supply Chain function
- Seek and support process improvement opportunities.
- Veeva activities to supported study leads/studies
- Participate in management monitoring activities for Pre-Production Management
- Support aligned Supply Chain Planners & Study Chain Study Leads as required
- On-time execution of pre-production tasks (such as PMD Manufacturing Request (MRs) approval) in order to maintain the supply of clinical trial material
- Right first-time documentation completion
- Management of temperature excursions for local depots, in-transit excursions from local depots, and clinical site excursions
- Veeva activities to support study leads/studies for maintaining integrity of clinical trial information.
- Quality - Management monitoring audits
- Approval of GMP MRs in local inventory management system (PMD) for both internal and external packaging activities.
- Management of inventory: movement of stock around the network as required ensuring the right stock is in the right place at the right time, timely destruction of expired materials
- Maintenance of demand plans within local MRP system (Supply Management Tool) in conjunction with the Supply Chain Study Lead / Planner within Clinical Interface
- Management of temperature excursions at clinical sites, ensuring all relevant documentation is retained in the appropriate archiving / trial master file system.
- Understand processes across the supply chain in order to ensure timely and accurate delivery of both information and documentation to the next node in the supply chain
- Ownership of the post-packaging assessment and release for new and additional countries participating in clinical studies
- Capable of accurately reviewing, editing and approving documentation for completeness, with attention to detail.
- Demonstrates an understanding of clinical packaging and manufacturing terminology.
- Possesses working knowledge of Good Manufacturing Practices (GMPs).
- Able to manage own time and workload priorities, self-motivated.