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 requiredKey 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 studiesRequirements:



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