Kedrion Biopharma
Mariangela Penta is a Computer System Validation Senior Associate at Kedrion Biopharma since May 2019, specializing in documentation processes for computerized systems to ensure compliance with current regulations. Prior experience includes a role in IT Compliance at CTP SYSTEM, where consulting on IT and QA compliance, managing the lifecycle of computerized systems, and conducting compliance assessments were key responsibilities. Mariangela also worked as an R&D engineer at MMI Srl, focusing on designing a sensorized tool for robotic micro-surgery, and as a project engineer at CNR-IFC, involved in the development of automated systems for producing gel-like microspheres. Educational qualifications include a Bachelor's and a Master's degree in Biomedical Engineering from the Università di Pisa.
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Kedrion Biopharma
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Kedrion Biopharma is a biopharmaceutical company that collects and fractionates blood plasma to produce and distribute worldwide plasma-derived therapies for use in treating and preventing rare and serious diseases and conditions. In 2022, Kedrion joined forces with BPL (Bio Products Laboratory). Based in the United Kingdom, BPL has over 60 years of experience in the supply of high-quality plasma-derived medicines to treat rare diseases. Kedrion distributes its products in over 100 countries around the world. We have plants in Italy, Hungary, UK and North America, and plasma collection centers in the US and in the Czech Republic. With these figures we are the world’s 5th top player in the field of plasma-derived products. Our goal is to build a diverse and professional workforce, providing job opportunities for talented external candidates as well as internal employees who aim to grow with us. Because our work includes so many interests and skills – from Research to Sales; Plasma Collection to Production – there are abundant possibilities for learning and growth. Kedrion builds bridges: from donors to patients, from plasma to therapies, from challenge to hope.