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OPERATIONS - CONSULTING
Clinical Trial Distribution Material Coordinator
Permanent contract
· Partners with supply planning to understand delivery schedule and priorities; partners with quality, Clinical and hub/depot for delivery execution activities
· Monitors deliveries due list for all shipments
· Resolves issues with hub/depot and manages deviation investigations related to all shipments as needed
· Accountable for shipping documentation availability with hub/depot; Ensure completion of any pre-shipment paperwork and ensures necessary import approvals are in place prior to shipment execution
· Ensures execution of the delivery in-time to meet the demands at the receiving plants
· FFU determinations in case of temperature excursion
· Identify related errors within IT systems,
· GMP Compliance
Ø Must be knowledgeable on how to apply GMPs in a clinical trial environment and review and follow procedures applicable to the CT business. In addition, individual training plans must be kept up to date.
· Ensure compliance with GDP/GMP of activities performed on behalf of our client knowledgeable on how to apply GMPs and GDPs in a clinical trial environment and follow procedures applicable to the CT business
· Ensure all internal and external regulatory requirements are met for Importation, warehousing, labelling and distribution activities for all type of products
· Participate or co-lead cross zone communication meetings
· Participate in the Metrics review meetings with the zone and distribution leadership
· Participate in the Metrics review meetings with couriers
· Participate in the creation and update of the C.T. Distribution processes, and the training to our clients
· Proactively identifies ways to improve day-to-day activities and practices. Support efforts to improve productivity, efficiency, product quality and reduction of risk through the use of the Six Sigma methodology
· Review and approve invoices received from distribution vendors
· Participate to visits to Hubs/Depots and Affiliates
· Support conference calls/meetings with Hubs/Depots/Affiliates and generate minutes
· Participate in projects linked to distribution process changes, including participate in the associated change control
· Confidentiality: Ensure confidentiality of information
Life sciences
2F044EE46F794190B704F6A8675FF5B1@ts.com
Europe, Belgium, Wallonia, Walloon Brabant
1-2 days per week
5. Bachelor Degree
3 to 5 years