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Clinical Supply Chain Associate Breda SIRE Life Sciences

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Gevraagd

  • 37 - 40 uur
  • Engels (taal)

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  • Vast contract
 

Vacature in het kort

Breda
Our client plays a vital role in the global supply chain by labeling, assembling, storing, and shipping medicines worldwide. You'll translate study requirements into global supply plans, manage logistical conflicts, and oversee labeling and shipment. Read on to discover why this challenge awaits you.
 

Over het bedrijf

SIRE Life Sciences
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The Company 
Our client plays a critical role in the global supply chain by labelling, assembling, storing, and shipping medicines to countries worldwide. With a diverse team of over 1,000 employees from 38 nationalities, they are dedicated to manufacturing, marketing, sales, and clinical research to advance innovative medicines for patients globally. 

Role Description 

As junior Global Supply Planner you work on ensuring supplies for clinical studies that run global and mostly under the supervision of an experienced planner. You will be working on the largest and fast lane trials. After training and proven experience, you will be working independently on less complex studies. The planning team works to reach a minimum of 99,99% for patient dosing with decision making on the right inventory levels at central warehouses and hospitals. During the entire length of the clinical trial, the study planner is responsible to update the demand for the global patient portfolio for the assigned studies and monitor supply at all locations to minimize product waste 

Responsibilities 
- Translate study team requirements into a clear global supply plan. 

-Support demand forecasting and planning meetings to ensure adequate supply strategies. 

-Act as a secondary liaison with study teams, Quality, and Regulatory Affairs to maintain forecasts and supply plans. 

-Resolve logistical conflicts to keep studies on track. 

-Oversee labeling, packaging, and shipment of supplies. 

-Identify and escalate supply chain risks to stakeholders and management. 

-Use systems to manage key product and project activities effectively. 

-Help stakeholders understand clinical supply chain processes and strategies. 

-Review, update, and develop procedures and SOPs as needed. 

Requirements: 

-Bachelor’s degree in Supply Chain, Business Administration, or related field. 

-At least 6 months of relevant experience in supply chain or clinical environments. 

-Fluency in English, both written and verbal (Dutch preferred). 

-Proficiency in MS Office; experience with ERP systems (preferably SAP) is a plus. 

-Ability to work in a fast-paced, regulated environment. 

-Strong analytical skills and the ability to communicate across teams. 

Other information: 

Interested? Please apply via the link or contact Sofia Alftan  

54596

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