Job Description

Job ref: QCVA Job type: Permanent Location: Newry Closing date: Monday 16 Feb :00 Job Overview Based within the QC Validation Department, the successful candidate will be involved in carrying out chemical analysis of in-process / finished product samples, collection and analysis of cleaning validation sampling, analytical method validation and completion of all associated documentation in accordance with the relevant validation protocols, and standard operating procedures (SOPs). Main Activities/Tasks The role will involve use of the following standard techniques: Wet chemistry UV/Vis Spectrometry Potentiometric analysis Karl Fischer moisture determinations High Performance Liquid Chromatography / Ultra Performance Liquid Chromatography (HPLC & UPLC) Dissolution Gas Chromatography (GC) Atomic absorption spectrometry (AAS) Other duties will include preparation of QC Validation Protocols, QC Validation Reports, Validation Master Plan and SOPs to support the cleaning validation program....

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