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.
#J-18808-Ljbffr