Description
QC Method Validation Analyst
Permanent
Lancashire - commutable from Preston, Bolton and Wigan
£22,000 - £25,000 per annum
My client, a pharmaceutical company based in Lancashire, is looking to recruit a QC Method Validation Analyst to join their QC department. The QC Method Validation Analyst will be responsible for Analytical Method Validation of existing test methods to ICH guidelines.
KEY DUTIES AND RESPONSIBILITIES:
As the QC Method Validation Analyst you will be required to perform a broad range of responsibilities, including but not limited to:
* Writing of protocols for analytical method validations as per ICH guidelines, validation report writing and investigation of non-conformance (OOS) and deviations.
* Execution of analytical work followed by reporting and recording of the results.
* Some method development will be required following the method validation
The successful candidate will:
* be degree qualified with at least a BSc in a chemistry-based discipline. In addition you will have previous experience validating methods to ICH guidelines.
* have pharmaceutical industry experience using instrumentation including HPLC, GC, UV, IR and KF. In addition you will need to have hands on experience of using Chromatography Data Systems.
* have extensive experience with analytical method validation ICH guidelines as well as method development and troubleshooting.
* must have previous experience in method validation and be knowledgeable on which column to use, retention times, changing the pH, linearity etc.
If this sounds like you and you want to join a growing pharmaceutical company then please apply now!
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