- You will carry out the analysis of raw materials/ in process/ finished product samples in accordance with cGMP standards.
- You will preform analytical testing methods such as HPLC and Dissolution.
- As the QC Analyst you will also have to analyse stability, validation and investigational samples as directed.
- You will be ensuring the Right First Time KPI (with respect to your documentation) is achieved and will be responsible for reviewing other analysts documentation to ensure no errors are present.
What you will need;
As the QC analyst you will need a BSc. in science or a related discipline with 18 months experience in the pharmaceutical industry where you would carry out HPLC, GC and IC testing. In the case of inaccurate results you will need to be able to identify, troubleshoot and follow up accordingly.
For more information on this position feel free to reach out. (01)47 44 692 or email@example.com.
Following your application for this specific role, Sigmar may contact you regarding other positions that we feel you may be suitable for. If you do not wish to be contacted about other opportunities please let us know. For further information please refer to the Privacy Statement on our website.