•Generating, implementing and/or reviewing master and completed qualification protocols related to the cleaning validation of equipment and components involved in the manufacturing processes
•Analyzing the results of testing and deciding the acceptability of results against pre-determined criteria
•Assuring revision of protocols and procedures CV related for conformance to regulations, SOPs, specifications and other applicable acceptance criteria
•Investigating problems which occur and determining solutions or recommendations for changes and/or improvements
•Reviewing, editing and approving deviation investigations, corrective actions, change controls, SOPs, reports and other documentation
Titolo di studio:
Laurea Magistrale - Chimico / Biologico / Ambientale
Lingue conosciute:
Inglese: Comprensione Ottimo
Disponibilità oraria: Full Time
Patente: B
Osservazioni: Facilitare e verificare la corretta applicazione delle norme cGMP in tutte le attività di convalida equipment e sistemi, coinvolti nella produzione, controllo e cleaning dei farmaci in ottemperanza alle norme GMP