15 ott - Siena
Altro
A leading biotech company in Italy is seeking a highly motivated Process & Computer System Validation Specialist (GCP) to join their QA department. 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. This is a full-time position offering a dynamic work environment focused on quality and innovation.
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