CY Partners Scientific Recruitment - Supply Chain Analyst

Job Title:

Supply Chain Analyst

Category:

Technical roles

Closing Date:

22/09/2025

If you are interested in this position please email your CV to Jack.Ramshaw@CYPartners.co.uk

Supply Chain Analyst - Clinical Trials
Location: Ware
Contract Type: 12 Month Contract
Working Pattern: Hybrid - 2 days on site, 3 days WFH
Salary: Up to £21.05 p/h 

We’re seeking a detail-oriented and proactive Supply Chain Analyst to support key pre-production and temperature excursion management activities within Global Packaging Operations and Clinical Interface teams. This is an exciting opportunity to play a critical role in the timely delivery of clinical supplies to patients across the globe.

Key Responsibilities:

• Execute and manage pre-production tasks to enable on-time handover of packaging jobs.

• Approve GMP Manufacturing Requests (MRs) in local inventory systems for internal and external packaging activities.

• Accurately complete documentation with a focus on quality and right-first-time principles.

• Manage and document clinical site temperature excursions, in-transit excursions, and depot excursions to ensure uninterrupted clinical supply.

• Conduct Veeva system activities to support clinical study leads and maintain the integrity of clinical trial information.

• Participate in management monitoring activities, supporting audit readiness and quality compliance.

• Collaborate with aligned Supply Chain Planners and Study Leads to maintain demand plans in local MRP systems (e.g., Supply Management Tool).

• Manage inventory across the network to ensure correct stock placement and timely disposal of expired materials.

• Own the post-packaging assessment and release process for new countries joining clinical studies.

Qualifications & Experience:

• University degree or equivalent experience in a relevant discipline.

• Proficient in Microsoft Office applications, particularly Excel, Word, and Outlook.

• Solid understanding of GMPs and clinical packaging/manufacturing processes.

• Experience working with document/quality management systems is desirable.

• Ability to accurately review and approve documentation with strong attention to detail.

• Self-motivated and capable of independently managing workload and priorities.

If this role sounds interesting to you apply now with a copy of your CV!