Stability Coordinator

Company: Intertek
Apply for the Stability Coordinator
Location: Cambridgeshire
Job Description:

Overview

In this role you coordinate pharmaceutical stability activities within a GMP laboratory setting, ensuring samples, records and equipment are managed accurately and compliantly. You will join the Stability Team in Melbourn and contribute to timely stability studies while receiving comprehensive training. This position offers an entry path into a regulated laboratory career with clear development opportunities. You help maintain quality, safety and regulatory alignment in a fast-paced environment, supporting cross-functional teams to meet daily timelines.

Pay / Benefits

  • competitive salary/benefits
  • development and career opportunities
  • inclusive workplace
  • Real Living Wage employer
  • global network of colleagues
  • dynamic working environment

Responsibilities

  • Coordinate day-to-day stability and sample management activities
  • Operate temperature- and humidity-controlled storage areas and equipment
  • Handle routine and ad-hoc sample storage, retrieval, preparation and disposal
  • Maintain accurate hard-copy and electronic stability records
  • Organise and dispatch samples to internal/external labs and clients
  • Support facility and equipment checks, including preventative maintenance
  • Plan workload to meet daily timelines and shipment deadlines
  • Communicate clearly within the stability team and wider lab groups
  • Work with Stability Team Leader to gain autonomy as experience develops

Key requirements

  • Highly organised with strong attention to detail
  • Ability to follow clear instructions and processes (training provided)
  • Methodical and reliable approach to routine, process-driven work
  • Comfortable with paperwork and record-keeping
  • Clear written and verbal communication skills
  • Ability to work independently and take responsibility for tasks
  • Role involves some manual handling and movement across two floors without a lift
  • Early morning availability to support stability pulls and 12:30pm shipment deadline
  • Experience in GMP, laboratory, logistics or regulated environment (desirable)
  • Transferable experience from administration, logistics, warehousing, retail operations
  • Scientific qualifications or laboratory experience (preferred)
  • Highly organized
  • Attention to detail
  • Strong written and verbal communication
  • GMP/regulatory environment familiarity
  • Stability storage operations (temperature/humidity control)
  • Documentation and record-keeping (electronic and hard-copy)

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Posted: November 1st, 2026