I am a biologist by training with more than 10 years of experience in cellular biology (cell culture and signal transduction), bioassay and biochemistry. I am the author of 5 papers published on peer-reviewed international journals.After my PhD in neurosciences, I worked in a biotech company for 7 years, applying cGMP requirements to the upstream phase to produce recombinant products (mainly monoclonal antibodies) and I participated in the upstream process development and validation.I have hands-on experience in drafting and revising GMP documentation relating to upstream manufacturing activities (SOPs, MBR, Action Plans and Protocols).I am a precise, detail-oriented, pragmatic, and well-organized person. My analytical mindset has always aided me to tackle challenges in the scientific field and to look for solutions to unpredictable difficulties. I have good communication and interpersonal skills. I work well in multidisciplinary teams, aware that each different background and competency is crucial to achieving the final goal.At LS Academy I will reinvent my scientific background and experiences, aiming to provide the best services to meet clients’ demands.For our training activities, I look for the most relevant and discussed topics in life sciences, from GMP compliance to medical device regulation passing through medical writing.Once identified, our mission is to provide not only the most detailed and up-to-date information (which our expert teachers do assure) but also to effectively convey those concepts through a two-way contextualizing approach, which favours a direct and effective discussion of case studies and real-life examples.For our medical writing services, I work as the connection point between the client and the team of expert Medical Writers we collaborate with. Our shared task is to assure that the required medical writing support will be provided, fully meeting the client’s demands.