Supply Chain Analyst

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.

Location: Ware, UK, GB

Posted Date: 9/9/2025