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Logistics & Supply Chain Coordinator 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
Join a global leader in biotechnology, dedicated to turning scientific discoveries into therapies for serious illnesses. The company operates a major logistics hub in Europe, ensuring high-quality and compliant services. The CW Associate Supply Chain role focuses on reverse logistics and operations support across the EMEA region. Key tasks include managing returns, handling distribution complaints, and ensuring compliance with regulations. Collaboration and continuous improvement are central to the role. Continue reading to see why we could be your next step.
 

Over het bedrijf

SIRE Life Sciences
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About the company:
Join a global leader in biotechnology with a strong European presence, committed to transforming scientific discoveries into therapies for patients with serious illnesses. The organization operates one of the largest logistics and packaging hubs in Europe, strategically positioned to serve global markets with high standards in quality and compliance. Their site in the south of the Netherlands functions as a pivotal point in the commercial supply chain, playing a crucial role in late-stage product development and lifecycle management for both commercial and clinical products 
 

About the Role 

The CW Associate Supply Chain – Reverse Logistics and Operations Support will play a vital role in supporting daily operations related to reverse logistics, distribution complaints, serialization, and tracking activities across the EMEA region. The role ensures compliance with regulatory requirements (GDP, SOX, GMP) and supports key supply chain processes in collaboration with various internal and external stakeholders.

Responsibilities
  • Coordinate FDP returns, CMOs, warehouses, or LSPs, including recalls.

  • Manage low-risk distribution complaints and ensure regulatory-compliant documentation.

  • Support serialization tracking and tracing under the Global Distribution Hub.

  • Analyze NMVO alerts and manage EU FMD trend reporting.

  • Ensure returns and complaints meet KPIs and compliance standards.

  • Maintain compliance with GDP, SOX, and GMP regulations.

  • Support audits and represent the team in stakeholder meetings.

  • Drive continuous improvement initiatives.

    Requirements: 

  • Critical thinking and analytical problem-solving.

  • High attention to detail with a quality-first mindset.

  • Ability to thrive in a fast-paced, regulated environment.

  • Skilled in reporting and technical writing.

  • Culturally adaptable and collaborative.

  • Proactive, self-motivated, and capable of working independently.

    Other information:
    Interested? please apply via the link below!

55364

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