- Expiry Date: 30 July 2021
Assists in the development, validation and implementation of LC-MS/MS assays for analysis of clinical and non-clinical pharmacokinetic or toxicokinetic samples in a GLP-like or GLP environment. Assists in the preparation of validation and other analytical reports. Perform bioanalytical testing of study samples using validated methods. Contributes to reporting study sample results to clients following the departmental policies and procedures. Assists in troubleshooting assays when problems arise.
Ensures compliance with and maintains required training in client and departmental GLP, SOP, safety and other departmental guidelines. Ensures that notebooks and other documentations are up-to-date as per departmental guidelines. Works relatively independently to meet short term goals and objectives. Operate and maintain LC-MS equipment.
BS or MS degree in chemistry, biochemistry or related scientific discipline with 1-3 years of experience, preferably in a bioanalytical laboratory.
Prior experience running HPLC or LC-MS instrumentation.
Watson LIMS experience is a plus.
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