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Valeria Pisani has worked in various roles in the medical device and research industries since 2009. In 2009, they completed an internship in quality control laboratory at Enologica Vason. In 2014, Valeria was a Visiting Researcher at Cardiff University, where they conducted mechanical and biochemical analyses of biopsied and cultured cartilage. From 2016 to 2021, they held various roles including Product Specialist & Key Account Specialist at MYSPINE Healthcare, Organizational Secretariat at Sonopain, and Medical Devices Compliance Consultant at PQE Group. Most recently, they have been Quality Assurance Manager at KLISBio, where they have been responsible for improving and adapting the Quality System to be ISO 13485 + 21 CFR 820 compliant.

Valeria Pisani has a diverse educational background. Valeria obtained a Bachelor of Engineering (BEng) in Biomedical Engineering from Politecnico di Milano in 2013. Valeria then completed a Master of Engineering (MEng) in Clinical Engineering from the same institution. In 2014-2015, they also completed a Master of Science (MSc) in Erasmus placement from Cardiff University / Prifysgol Caerdydd. Valeria has also obtained various certifications, including a Six Sigma Black Belt (CSSBB) from CHIARINI & ASSOCIATI - CHIARINI & ASSOCIATES in 2022, an Auditor/Lead Auditor of Quality Management Systems - ISO 9001:2015 and EN ISO 13485:2016 from TÃœV SÃœD in 2021, Statistical Quality Analysis (SQA & ASQA) from Minitab Italy in 2021, Training on clean room, EtO sterilization and microbiological test from Silk Biomaterials in 2021, Lean Six Sigma Green Belt (ICGB) from 6SIGMAstudy - The global certification body for six sigma certifications in 2020, and a TOEIC: Test of English for International Communications from Eas Milan in 2013.