Associate Supply Chain (GMP)

Associate Supply Chain (GMP) bij toonaangevend biotechbedrijf in Breda, verantwoordelijk voor klinische distributie en temperatuurbeheer.

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Schijnopdrachtsignaal. Opvallend plaatsingspatroon; geen bewijs dat de opdracht niet bestaat.

SIRE Life Sciences B.V. plaatste deze aanvraag in 3 weken 2 keer opnieuw, gemiddeld om de 10 dagen.

Deze markering komt uit herhaalde plaatsingen of dezelfde rol op meerdere locaties tegelijk. Zo herkennen we plaatsingspatronen.

Bekijk bij SIRE Life Sciences B.V. (opent in een nieuw tabblad)

Eisen

  • Minimum 2 years of prior experience in supply chain management, preferably within a regulated environment
  • Bachelor's degree in Supply Chain Management or a related field
  • Strong understanding of regulatory guidelines affecting clinical supplies
  • Proficiency in English, both spoken and written
  • Experience working with automated business systems, such as MS Office suite
  • Familiarity with ERP systems
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Volledige omschrijving

A leading biotechnology company dedicated to serving patients worldwide. The organization operates a global supply chain network, manufacturing and distributing medicines and clinical research products. With a diverse team of professionals from multiple countries, it focuses on innovative healthcare solutions and improving patient outcomes. We are seeking a detail-oriented and experienced Clinical Supply Chain Associate to join the team. In this role, you will oversee the efficient and compliant distribution of investigational products to clinical sites around the world, ensuring timely delivery and adherence to regulatory standards.

Responsibilities: manage the sales order and stock transfer order processes efficiently; review temperature data and manage temperature excursions, ensuring compliance with regulatory standards; control and monitor the site and transit temperature excursions, as well as handle returns and reconciliations; support expiry relabeling campaigns and manage import licenses; process and handle distribution complaints promptly; ensure timely and compliant shipping of investigational products to clinical sites and logistics service providers; collaborate closely with Clinical Customer Service, Development Supply Chain stakeholders, QA, warehouse teams, clinical site monitors, and couriers to resolve issues swiftly; review and manage temperature data reviews and excursions, maintaining accurate documentation and KPIs.

Requirements: Bachelor's degree in Supply Chain Management or a related field; minimum 2 years of prior experience in supply chain management, preferably within a regulated environment; proficiency in English, both spoken and written; strong understanding of regulatory guidelines affecting clinical supplies; familiarity with ERP systems; experience working with automated business systems, such as MS Office suite. If you are interested and want to apply, please submit your application via the apply button.

Bekijk bij SIRE Life Sciences B.V. (opent in een nieuw tabblad)

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Associate Supply Chain (GMP)

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