Supply Chain Analyst
5 days ago
Ware
Start date: asap Contract duration: 12-month contract Location: Ware – 2 days per week on site PAYE rate: £157.67 per day Job Purpose: • 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 Key Responsibilities: • 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 Requirements: University degree or equivalent experience, plus demonstrated computer skills in Microsoft office suite of products. • 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.