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Interim Supply Chain Administrator £207pd

Interim Supply Chain Administrator £207pd

  • Location

    Hertfordshire

  • Sector:

    Supply Chain

  • Job type:

    Contract

  • Salary:

    £150 - £207 per day

  • Contact:

    Claire Shipman

  • Contact email:

    claire.shipman@1st-executive.com

  • Job ref:

    CS870_1755688005

  • Published:

    1 day ago

  • Duration:

    12 months

  • Expiry date:

    2025-09-19

  • Startdate:

    ASAP

Supply Chain Administrator - £207 per day

Role: Interim Supply Chain Administrator (Global Packaging Operations)

Rate: £207 per day (Umbrella, Inside IR35)

Client: Leading Pharmaceuticals organisation

Location: Hybrid working from home and 2 days per week in Hertfordshire

Duration: 12 months

Are you detail-oriented, highly organised, and motivated by supporting life-changing clinical trials?

A FTSE 100 Pharmaceuticals organisation is looking for a Supply Chain Administrator to join their Global Packaging Operations team and play a key role in ensuring the smooth delivery of clinical supplies worldwide.


What you'll do:

In this role, you'll be at the heart of this organisation's Clinical Supply Chain function, supporting both the Global Packaging Operations and Clinical Interface teams.

Responsibilities will include:

  • Carry out inbox monitoring for any quality issues identified with clinical supplies, on clinical trial sites.

  • Work closely with Quality Teams to support the decision on viability of clinical supplies.
  • Manage and approve temperature excursions at clinical sites and depots to ensure continuity of supply.

  • Support Study Leads with documentation and ensure information remains accurate.

  • Monitor inventory, coordinate stock movement, and ensure timely destruction of expired materials.

  • Support process improvement initiatives and participate in quality monitoring audits.


What we're looking for:

  • Strong organisational skills, with the ability to manage your own time and workload effectively.
  • Strong IT skills, particularly with the Microsoft Office Suite.

  • Ideally, any experience with GMP (Good Manufacturing Practice) within Quality.
  • Proven ability to review, edit, and approve documentation with accuracy.

  • Advantageous would be any experience in Clinical Trials.

This is an urgent requirement - if interested, please apply asap and any questions, email claire.shipman@1st-executive.com