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A pharmaceutical company in Madrid is seeking an experienced QC Supervisor to manage daily laboratory operations. Responsibilities include supervising lab activities, releasing raw materials, and issuing analysis certificates. The ideal candidate holds a degree in Analytical Chemistry, has experience in GMP environments, and demonstrates strong planning and communication skills. Fluency in English and Spanish is required. The position offers an indefinite-term contract with a salary plus bonus and a detailed training plan, operating under a shift schedule.
As Qc Supervisor under supervision of the QC Laboratory Analysis Manager , will be responsible for the daily management of the QC Laboratory performing the following functions :
Coordination and supervision of the activities carried out in the QC Laboratory.
Release and / or rejection of raw materials and intermediates in the system.
Management, issuance and signature of certificates of analysis sent to customers.
Technical support to the analysts during the analysis and in all the activities related to the laboratory, as well as their continuous training.
Editing of the weekly and daily planning and distribution of tasks of the analysts to achieve the fulfillment of the planning.
Investigation of unexpected results (out of specification and / or out of trend) obtained in the laboratory.
Issuance of investigation reports of unexpected results for CMO products.
Notification and investigation of deviations generated.
Collaboration in the elaboration and / or control of the KPI's of the department.