VIVEbiotech is a GMP Contract Development and Manufacturing Organization (CDMO) specialized in Lentiviral vectors.

Biotechnology

Manufacturing

VIVEbiotech

VIVEbiotech's headquarters in San Sebastian, Spain

Lopez De Maturana

Cristina Valderrey Labiano

Maria Soledad Fernandes Oñederra

The Quality Assurance and Control team at VIVEbiotech ensures that all processes and products meet stringent regulatory standards and internal quality specifications. They are responsible for monitoring and validating manufacturing practices, conducting quality audits, and performing analytical testing on Lentiviral vectors to guarantee product safety and efficacy. Through their systematic oversight, they help maintain the integrity and reliability of the biotechnological processes essential to the company's operations.

Quality Assurance and Control

The Manufacturing and Production Specialists team at VIVEbiotech oversees the entire production process of Lentiviral vectors, ensuring compliance with GMP standards. This team collaborates on both upstream and downstream manufacturing operations, focusing on optimizing production efficiency, maintaining quality control, and implementing innovative techniques to support the development of advanced therapeutic solutions. Their expertise ensures the timely and reliable delivery of high-quality biopharmaceutical products.

Manufacturing and Production Specialists

The Research and Development team at VIVEbiotech focuses on advancing the design and production of Lentiviral vectors. This multidisciplinary team collaborates on upstream and downstream processes, analytical methods, and innovative approaches to enhance vector efficiency and safety. Their expertise drives the development of robust manufacturing protocols, ensuring high-quality gene therapy products for clients in the biotechnology sector.

Research and Development

The Technical Support and Operations team at VIVEbiotech plays a critical role in ensuring seamless manufacturing and quality assurance processes for Lentiviral vector production. This team is responsible for coordinating logistics, managing and supporting technical operations, and addressing customer inquiries, while maintaining compliance with GMP standards. Their collaborative efforts align various functions, from upstream and downstream manufacturing to quality control, to deliver high-quality biopharmaceuticals efficiently.

Technical Support and Operations

The Project Management and Coordination team at VIVEbiotech is responsible for overseeing and coordinating the development and manufacturing processes of Lentiviral vector projects. They ensure alignment between various stakeholders, manage timelines and resources, and facilitate communication to drive projects to successful completion. By leveraging market research and technical expertise, the team aims to optimize project outcomes and support business growth.

Project Management and Coordination

The Technology and Innovation team at VIVEbiotech is responsible for driving advancements in the development and manufacturing of Lentiviral vectors. This team leverages cutting-edge research and technology to optimize processes, enhance product quality, and ensure compliance with GMP standards, while also fostering collaboration between PhD students and experienced professionals to pioneer innovative solutions in biopharmaceutical manufacturing.

VIVEbiotech

Org chart

Teams

Quality Assurance and Control

Manufacturing and Production Specialists

Research and Development

Technical Support and Operations

Project Management and Coordination

Technology and Innovation

Offices

VIVEbiotech

Org chart

Teams

Quality Assurance and Control

Manufacturing and Production Specialists

Research and Development

Technical Support and Operations

Project Management and Coordination

Technology and Innovation

Offices

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