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• Performing laboratory analysis based on documented analytical methods and procedures.
• Analysis to the appropriate test specification of raw materials, finished goods and any other routine and non-routine analysis as required.
• Participate in process validation work linked to routine manufacture of pharmaceuticals.
• Carry out routine internal calibration activities of laboratory equipment and ensure that all such equipment is maintained in good working order.
• Contribute to the writing of specifications, analytical methods and validation of methods.
• Contribute and participate in ongoing continuous improvement initiatives.
• Assist in meeting ongoing metric driven goals and KPIs.
• Maintain neat and accurate analysis records.
• Organising and prioritising own workloads to meet deadlines.
• Support H&S and COSSH tasks as and when required.
• Participating in periodic Reference Standard and chemical stock checks
• Undertake analytical training courses, where necessary, to develop key skills deemed critical to business needs.

• A degree in Chemistry, or a closely related subject, or suitable industry experience.
• Experience working in an analytical laboratory with a good knowledge of GLP.
• Able to work to strict deadlines.
• The ability to work under pressure and to deadlines – (this role will necessitate working additional hours and/or shifts as and when required).

• Knowledge of the pharmaceutical industry, analytical method development and validation and the calibration of equipment.
• Knowledge, use and maintenance of HPLC, AA, UV, FTIR, Potentiometric Titration and GC.
• Knowledge and experience working to ICH Quality guidelines for Validation.

Job Segment: Laboratory, Pharmaceutical, Chemical Research, Science, Engineering