Patrizia Muscas PhD Eli Lilly and Company

31 years of experience in Pharmaceutical and Biopharmaceutical field. Experience raised working with International Companies (GSK; Chiron Vaccine; Eli Lilly). During these years of experience, I had the responsibility of the management of Microbiological and Biological pharmaceutical control laboratories, and I have been involved, as project team member, in validation and improvement of production sites for Sterile liquids, Dry powders, Vaccines, and non-sterile products. For 9 years my primary role was dedicated to oversight of all sterility assurance aspect/topics with regards to the Eli Lilly Sesto production lines (Isolator and RABS technology). I was part of the teams involved in the new construction of these new lines departments with responsibility for all Sterility Assurance topics/strategies and on Isolator VPHP cycle and sterilization processes qualification/management. In the last years I covered the role of Leader of the team guarantying the oversight for all Sterility Assurance aspects of the Sesto Lilly parenteral site participating to all Global network activities on this topic. Since 2020 joined the Global TS-MS Sterility Assurance group with the role of Sr Lead Sterility Assurance supporting and interacting with the Global Network teams for all the aspects related to Sterility Assurance, Environmental Monitoring, VPHP decontamination process and Contamination Control strategies.