QC Analyst

An opportunity has arisen for an Analyst to join our existing QC team within the Pharmaceutical Development and Support (PDS) department. Key Responsibilities: Carry out the Quality Control of raw materials, bulk, and finished products in accordance with relevant authorised documentation using HPLC, GC, and wet chemical techniques. Perform swabbing and analysis of samples for cleaning verification of the pilot production facility. Take equal part in the overall running of the laboratory, including equipment maintenance, calibration of apparatus, and other general duties such as solvent disposal. Perform manual and automated tests and assays in accordance with GMP to a high level of accuracy and precision and operate associated analytical equipment. You should ideally have the following attributes: A minimum of a year’s relevant experience in an analytical testing role, preferably in a GMP environment. Some experience in the techniques of HPLC and GC analysis. Excellent attention to detail and organisational skills, and the ability to self-motivate under your own initiative. Collaborative skills to work closely with colleagues and managers. Use of software packages, such as Chromatography Data Handling, LIMS, and Excel, for the collection, processing, and reporting of data. Apply

If you are interested, to find out more or apply, please contact us on 01462 458866 or email your CV with a covering letter to:

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