09 ago - Siena
Philogen
A leading biotech company in Italy is seeking a highly motivated Process & Computer System Validation Specialist (GCP) to join their QA department.
Per il seguente ruolo potrebbero essere richieste diverse soft skill ed esperienze.
La preghiamo di consultare attentamente la panoramica riportata di seguito.
The role involves validating computerized systems to ensure compliance with GMP/GCP regulations, contributing to data integrity in clinical environments.
Candidates should have a relevant degree, at least 2 years of experience in the pharmaceutical sector, and a good command of English.
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This is a full-time position offering a dynamic work environment focused on quality and innovation.
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