Technologist / Documentation Coordinator
Location: Slough
Contract: 6 months
Start: ASAP
Pay Rate: £14 per hour
Overview
A hybrid role combining lab-based support and documentation coordination within a GMP-regulated pharmaceutical environment. You will support the Raw Materials team to ensure testing, scheduling, and documentation processes run smoothly and efficiently.
Key Responsibilities
- - Support testing of raw material samples and report results following GMP procedures.
- - Assist with entering results generated by other team members.
- - Follow all safety processes and GMP guidelines.
- - Manage archiving of assay forms and Raw Material Specifications (RMS).
- - Prepare RMS release packs for internal and external audits.
- - Provide vendor certifications when required.
- - Process RMS for release — ensuring accuracy, quality, and compliance.
- - Support monthly retain audit activities.
- - Coordinate day-to-day activities within the Raw Materials team, ensuring scheduling stays on track.
Skills & Competencies
- - Strong attention to detail and ability to maintain high-quality standards.
- - Ability to adapt to change, work proactively, and show initiative.
- - Understanding of chemical/biochemical testing techniques.
- - Confidence reviewing data and supporting junior team members.
- - Excellent organisational skills and ability to manage workload effectively.
Requirements
- - Experience in a GMP lab environment (pharma preferred).
- - BSc in Chemistry or Pharmaceutical Sciences preferred.
- - English — Business fluent.