quality control officer.

The main responsibilities as a Quality Control Officer will be the following:

• Overview the analyses results upon theri compliance to specification and enters the results to LIMS. 
• Participate in validation and transfer of analytical methods as well as in factory validation (cleaning validation,process validation), by evaluation  the upcoming results 
• Supervise and coordinate the chemical analyses required according to the stability program 
• Support the training of laboratory personnel 
• Report any problems that appear during the analysis (OOS) and contributes to their resolution 
• Overview the maintenance of standards, chromatography columns and liquid and solid reagents and solvents 
• Monitor the calibration and maintenance program of the equipment and informs respectively the QC Manager and the competent external partner 
• Check the operations;l status and reliability of laboratory equipment and repost any operations problem to the QC Manager 

• 4-5 years or previous relevant working experience within the pharmaceutical industry

• Bachelor or Master ‘s degree in Chemistry, Biology, Chemical Engineering or other related field
• ability to work with a high level of autonomy and handle complex/difficult situations