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An established industry player is seeking a Procurement Coordinator to join their dynamic team in Bristol. This role is pivotal in ensuring the timely and cost-effective procurement of essential materials for the development of advanced therapies. You will engage with a globally recognized team, enhancing your skills in procurement and supplier management while adhering to strict regulatory standards. This exciting opportunity offers the chance to contribute to groundbreaking projects in the biotechnology sector, making a real impact in a rapidly growing market.
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bristol, United Kingdom
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05.05.2025
19.06.2025
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Job title: Procurement Coordinator 2 (12-month Fixed Term Appointment)
Reporting to: Procurement and Warehouse Manager
Department: GMP Operations
No of Direct reports: 0
Location: Bristol
Summary:
eXmoor helps clients with their manufacturing of cell and gene therapies (CGT) and biopharmaceuticals. We provide; (1) translation consultancy to close the gap between R&D and clinical manufacture, (2) process development services from our wet labs in Bristol (3) capital project design through to licensing and (4) GMP manufacturing for early phase clinical trials.
We are looking for a Procurement Coordinator to support sourcing, supplier management and procurement operations at the Cell & Gene Therapy Centre, Bristol. This role is crucial in ensuring the timely and cost-effective procurement of critical materials, consumables and services for process development and clinical manufacturing of ATMPs (Advanced Therapies Medicinal Products).
This is an exciting opportunity to work with eXmoor’s globally recognised team of scientists, consultants, and engineers, on a wide range of Client projects in a rapidly growing market.
Job Description:
Job Purpose:
The Procurement Coordinator will support the Procurement and Warehouse team with purchasing and inventory management activities on behalf of the Process Development (PD) and GMP Operations teams at eXmoor. The Coordinator is responsible for the sourcing of materials and services in a cost-effective manner, in compliance with Good Manufacturing Practice (GMP) and other regulatory guidelines as required.
Main areas of responsibility/key duties:
Personal Specification
Essential Qualifications & Experience:
Desirable Qualifications & Experience:
Competences Required: