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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
What skills do you bring on the table?
· Bachelor/master’s degree, preferably in health care or supply chain/logistics field or equivalent work experience.
· Fluent in French and English
· Demonstrated knowledge of cGMPs and experience in a highly regulated environment Customer and process focused
· Understands global shipping requirements, including country-specific requirements
· Demonstrated exemplary teamwork/interpersonal skills
· Strong organization and self-management skills
· Ability to use and apply multiple computer applications
· Ability to manage multiple tasks and respond to change
· High initiative, flexible and positive attitude
· High degree of accuracy with work and attentive to details
· Ability to proactively identify problems and work toward a solution
What’s the offer you can’t refuse?
As an AKKODIS Team member, you will be:
· Onboarded in your position via a buddy process
· Supported in your c areer by your Business Manager
· Actor of your training plan and your personal and professional development
· Benefiting from a permanent contract
· Benefiting from a competitive salary package including several extra-legal benefits
Do you any questions? You can contact me at marie.defruit@akkodis.com
Europe, Belgium, Wallonia, Walloon Brabant
1-2 days per week
5. Bachelor Degree
3 to 5 years