GMP QA Training & Documentation Lead

04 set - Parma
Biopharma Careers

pChiesi is seeking a Training Documentation Specialist for Global TechOps Supply in Parma. You will oversee training and documentation systems, implement a new document management project, and coordinate governance for training software while ensuring regulatory compliance and audit readiness. /ppYou will liaise with cross-functional teams, manage access controls, and support regulatory audits, contributing to a robust quality framework and continuous improvement efforts. /p #J-18808-Ljbffr

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