Supply Chain Analyst - GSK0JP00106870

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.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.