Technologist / Documentation CoordinatorLocation: SloughContract: 6 monthsStart: ASAPPay Rate: 14 per hourOverviewA 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 and 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 ..... full job details .....