Elena Di Matteo
About
Elena Di Matteo is from Rome, Latium, Italy. Elena works in the following industries: "Pharmaceutical Manufacturing". Elena is currently Scientist in the R&D Department at Nouscom AG, located in Roma, Lazio, Italia. In Elena's previous role as a Junior Scientist at Nouscom AG, Elena worked in Roma, Italia until Dec 2019. Prior to joining Nouscom AG, Elena was a GMP Staff Scientist at IRBM and held the position of GMP Staff Scientist at Pomezia (RM), Italia. Prior to that, Elena was a Internship, Research Group Prof. Isabella Saggio at Department of Biology and Biotechnology "Charles Darwin", University "Sapienza" of Rome, based in Rome, Italy from Feb 2012 to Jul 2014.
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Elena Di Matteo's current jobs
• PEV UNIT Scientist (NOUS-PEV Clinical Trial Phase 1B), responsible of the generation of personalized immunotherapy in a pre-clinical setting; • Elaboration and optimization of internal procedures for the bioburden risk reduction and for the patient specific raw materials tracking; • Organization and planning of laboratories activities, spaces and material/reagents storage points; • Recording and reviewing of data and documents specific for each PEV drug product produced • Activity of optimization of viral vectors production to apply in the company's future pipeline products; • Develop new strategies and drug products reliable in the immunotherapy field looking at the unmet patient needs; • Presentations of scientific works to internal and external meetings.
Elena Di Matteo's past jobs
• Organizational and self-management of the experimental work • Set-up and strategy optimization of vaccines production for immunotherapy: cloning strategies, viral vectors production, flow cytometry, cell cultures , DNA and RNA analysis, protein expression assays. • Review and proof-reading of protocols and internal SOPs; • Clinical lots production • Presentations of scientific works to internal and external meetings.
• Manufacturing of viral based vaccines for phase I and II clinical trials • Clinical and tox lots production • Sterile filling of a clinical lots for phase I and II • Validation and maintenance of the GMP facility • Reviewing of Batch Manufacturing Records • Responsible of purchasing and managing of raw materials
• Planning and direct realization of in vivo and in vitro experiments • Collection, formalization and critical analysis of data. • Drafting and exhibition of scientific presentations.