To prepare reagents, solutions and working standards, foreseeing the need of purchases of inputs and reagents to support the necessary stock that allows to carry out tasks they are assigned him.
To carry out in time and fulfillment with methods and standard operative procedures, the analytical tasks of control physico-chemical who are assigned to him to check the level of fulfillment of the materials and products tested with regard to the current specifications
To collaborate with the execution of the activities proposed by other sectors of the company (transfers, validations, investigations, etc.)
To document adequately the activities that it realizes to assure the fulfillment with the procedure cGMP, the good practices of documentation and the current standard operative procedures.
To report results out of specification or abnormal situations that could impact on the quality of the production, offering necessary information in ideal time and facilitating the capture of corrective or preventive actions as corresponds.
To write and to collaborate in the redaction of operative procedures and analytical technologies linked with the tasks of the sector, taking part in the process of constant improvement.
The Candidate :
High school, chemical specialist, University student or graduates on Pharmacy or similar career
Minimum 3 years in laboratories of Quality control.
Knowledge of technical English to understand specific documents or Pharmacopeias.
Knowledge of using analytical techniques and laboratory equipment
Knowledge of using PC and Microsoft application
Very good documentation skills.
Potential for career
Defined career path and annual performance review & feedback process