Description
A leading pharmaceutical manufacturing company in Tipperary are hiring a QC analyst to join their QC laboratory. This is an exciting opportunity to join a growing, fast paced lab environment.As the QC analyst you will be responsible for:
*Sampling and analysis of blend samples, intermediates, in-process samples, raw materials, swabs, packaging components and finished product
*Raw material, in-process and finished product, stability and validation analysis using wet chemistry and other techniques such as HPLC, GC, Dissolution, KFT, FTIR, NIR, autotitrator.
*Instrument calibration
*Reagent and volumetric solution preparation
*Real time report writing and accurate documentation and record maintenance
*Filing of QC paperwork
*Waste Disposal
*Assisting in the ordering of laboratory chemicals and standards
*Assisting the analytical facilitator in LFI and ATD investigations and report writing
*Assisting in the updating of specifications, methods and procedures
*Assisting in Health and Safety issues
*Ensuring the laboratory area is clean, tidy and is inspection ready
*Procurement of samples, chemicals, reagents etc
*Involvement in stability testing
Requirements:
*Hold a relevant 3rd level science qualification
*Have a minimum of 2 years experience working in a pharmaceutical laboratory environment
*Experience in Chromatographic techniques particularly HPLC is essential
*Excellent knowledge of GLP
*Working knowledge of cGMP.
Salary 35K
If you are interested in this role and have the relevant experience contact Meadhbh Langton on or apply with your CV.
To find out more about Real please visit www.realstaffing.com