3PBIOVIAN
Pablo Gogorcena Burguete serves as the QA Audits and Compliance Head at 3PBIOVIAN since January 2024, overseeing internal audits and ensuring compliance with quality standards and regulations, as well as managing external audits. Previously, Pablo held the position of QA Audits and Supply Chain Head at 3P Biopharmaceuticals since May 2019, where responsibilities included internal and supplier audits as well as indicators management. Earlier experience includes roles in the quality department at Laboratorios Cinfa, focusing on compliance with FDA regulations. Pablo holds a degree in Chemistry with a diploma in Medical Chemistry from the University of Navarra and has completed master's degrees in Quality Management and SAP Software.
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3PBIOVIAN
3PBIOVIAN service offering includes microbial and mammalian protein expression platforms, viral vector production for adenoviruses and adeno-associated viruses, cell therapy, and plasmid DNA production, with the provision for fill and finish services for recombinant proteins and viral vectors. Leveraging a combined track record of 40 years in process development and analytical methods development, complemented by the experience in process scale-up, GMP manufacturing, and commercial supply, 3PBIOVIAN is equipped to offer comprehensive manufacturing services at all stages, encompassing Drug Substance and Drug Product. Manufacturing sites in Pamplona-Noáin, Spain, and Turku, Finland seamlessly support the diverse needs of clients, covering pre-clinical and clinical supply to full-scale commercial manufacturing.