The primary purpose of the Laboratory Analyst is to analyse raw material, in-process and finished product as well as stability samples according to the relevant specifications.
The QC Analyst shall carry out most of his/her duties in the QC Laboratory and the primary tasks and responsibilities of the position are as follows:
* Working as directed by the Area Supervisor, in accordance with Company safety policies, cGMP and cGLP.
* Receiving and logging samples into the Laboratory.
* Analysing raw material, in-process, finished product and stability samples associated with development products according to specifications.
* Performing analytical method validations and investigational testing as directed.
* Recording results in a timely and accurate fashion.
* Ensuring the Right First Time KPI with respect to Analyst's documentation are achieved.
* Reviewing co-workers/analyst documentation.
* Ensuring that all Quality Systems within the department are adhered to on a daily basis.
* Ensuring correct labelling of laboratory reagents and samples.
* Troubleshooting any erroneous analytical data obtained (Involvement in Lab Investigations Reports).
* Helping to ensure laboratory SOPs and specifications are kept up to date and in a state of compliance.
* Training other laboratory staff as requested and appropriate.
About you:
* Minimum of 2 years HPLC experience.
* Ability to troubleshoot, identify analytical issues and follow up with corrective actions.
* A minimum of a BSc in a science related discipline.
* Ability to critically review analytical data. Possessing excellent attention to detail is a must.
* The ability to work well with all key contacts both internal and external to the organisation.
* Experience working within a cGMP environment (HPRA and FDA approved) would be desirable.
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