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QC Technician (Analytical)
Job Type:
West Lothian
Exact Salary:
Date Posted:
16-May-2022 04:01 PM
Ref #:

Escape Recruitment are excited to be working a world-renowned scientific company to recruit a QC Technician (Analytical). Based in West Lothian, you will join an industry leading company who are committed to the development of vaccinations which focus on prevention of infectious diseases with significant unmet medical needs. With an emphasis on travel vaccines, my client aims to improve awareness, advice and access which will better protect travellers through working in partnership with healthcare providers. The QC Tech Analytical role will focus on Quality Control department tests for the release of raw materials, intermediate products and final products with best cGMP work practices, Quality Standards and metrics.


  • Execute analytical procedures, for testing of raw materials, intermediate products and final products, according to defined SOPs and protocols

  • Apply best cGMP work practices and techniques to test and release raw materials and product within specification

  • Ensure that all necessary training is complete in the procedures conducted, and operate in compliance with best cGMP working practices at all times and be accountable for the analytical laboratories being clean and tidy

  • Conduct all activities in the most careful and safe manner and in full compliance with HSE requirements

  • Support change controls, investigations and CAPA's in the post diligent manner

  • Assist in monitoring and maintaining calibration status of all equipment within the Quality Control department, including calibration of pipettes and informing relevant personnel in a timely manner of any failure of calibration

  • Arrange subcontract of QC testing and dispatch to approved suppliers and provide support to the Logistics department and preparation of SOPs

  • Perform filing duties and other QC administrative duties as required by the line manager or Head of QC


  • A minimum of 2 years' experience working within a QC laboratory working to GMP within a recognised quality system

  • Writing and working to SOP documentation

  • Analytical methods experience, in a production-focused environment, in assays (not limited to) Haemagglutination assays, micro-plate assays such as ELISA and dye binding colorimetric assays (Bradford Method, Coomassie Plus), Electrophoresis, TVC and UV Spectrophotometry

  • Assay development, validation and transfer experience desirable

  • Experience of working within Quality Management Systems which include deviations, change controls and CAPA's

  • Cell culture and Microbiological experience would be preferable

  • Plaque testing and ELISA experience highly desirable

  • Knowledge of GMP guidelines and regulatory bodies

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