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VIVEbiotech is a Contract Development and Manufacturing Organization (CDMO) headquartered in San Sebastian, Spain, specializing exclusively in the development and manufacture of…
- Locations
- San Sebastián only
- Work style
- All on-site
- Level
- Mid-Level for 5 of 7
- Locations
- San Sebastián only
- Work style
- All on-site
- Level
- Mid-Level for 5 of 7
Senior Project Manager
QA Technician
Engineering Projects Head
IT Systems and Projects Technician
Maintenance Technician
QC Laboratory Technician
About the company
VIVEbiotech is a Contract Development and Manufacturing Organization (CDMO) headquartered in San Sebastian, Spain, specializing exclusively in the development and manufacture of GMP-grade lentiviral vectors for gene and cell therapy applications. With over 10 years of experience, the company serves more than 50 biotech and pharmaceutical clients across the US, Europe, Asia, and Australia, offering comprehensive services from process development to clinical-grade manufacturing. VIVEbiotech operates 7 dedicated cleanrooms and has manufactured over 200 batches, positioning itself as a leader in the lentiviral vector field.
For International Professionals
- Headquartered in San Sebastian (Donostia), Spain, in the Miramon technology park, a hub for biotech innovation in the Basque Country.
- The company is 100% Guipuzcoan (Basque) in origin and has spearheaded the creation of a regional ecosystem specialized in health-related biotechnology.
- VIVEbiotech operates under both EMA and FDA regulations, offering international professionals experience in globally recognized quality standards.
- The team combines young talent with professionals having more than 30 years of experience in virology and production.
- The company has clients across the US, Europe, Asia, and Australia, indicating a highly international work environment.
Offices in Spain
Company History
VIVEbiotech was created in 2015 in San Sebastian, Spain, building on a legacy that began in 2004 with the establishment of an Advanced Therapies Unit. The company has since become a Contract Development and Manufacturing Organization (CDMO) specialized exclusively in the development and manufacture of GMP lentiviral vectors, serving over 50 biotech and pharmaceutical clients worldwide under EMA and FDA standards.