Usp/dsp Technician
hace 3 días
Leanbio is a fast-growing Contract Development and Manufacturing Organization (CDMO) specialized in the production of recombinant proteins and mRNA. We are dedicated to helping our clients bridge the gap between science and manufacturing, acting as catalysts for their research and innovation. Our tailored solutions empower breakthroughs in biotechnology.
Located in Barcelona (St Quirze del Vallès), a prominent biotechnology hub, we pride ourselves on delivering exceptional client-focused services while fostering a dynamic and innovative workplace environment.
We are looking for a QA specialist to join our team in our new facilities in Sant Quirze del Vallès that needs:
- Background in Biomedical sciences / Pharma / Biotech.
- 0-1 year experience in biotechnology industry.
- Technical knowledge in upstream process with expression platforms as bacterial, yeast or cell culture.
- Able to work in a cross-functional approach and work independently with mínimal supervision.
- Team player in an evolving environment.
- Strong interpersonal and communications skills; written and oral.
- Proficient in English (written and oral)
**Key responsabilities**:
- To execute process development programs at lab scale and pilot scale
manufacturing lots.
- To work under SOP procedures at expected quality standards.
- To participate in lab management tasks.
- Responsible for the performance of the operational activities to the required quality
and on time according to project timelines and (Senior) Scientist indications.
- Responsible for reporting the results according to company documentation
standards.
- Flexible Schedule, depending on process activities.
**We offer**:
- Opportunity for a powerful professional development and growth.
- Participate in the process department growth expected in the near future.
- Opportunity to work in a dynamic and challenging environment.
- Opportunity to work in a biopharma GMP located in Barcelona area (St Quirze), with multiple products/projects ongoing and perspective for market aproval of several products.
Tipo de puesto: Jornada completa
Sueldo: Hasta 40.000,00€ al año
Horario:
- De lunes a viernes
Idioma:
- inglés (Obligatorio)
Ubicación del trabajo: Empleo presencial
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