A biotech company specializing in biologics development and manufacturing, focused on accelerating drug discovery. It offers integrated services from cell line development to GMP production.

Background required

- Background in Biomedical sciences / Pharma / Biotech.

- 0-1 year experience in biotechnology industry.

- Basic knowledge in downstream process techniques such as chromatography and filtration (tangential flow filtration, depth filtrations, etc.).

- Able to work in a cross-functional approach and work independently with minimal supervision.

- Team player in an evolving environment.

- Strong interpersonal and communications skills; written and oral.

- Proficient in English (written and oral).

- Based in Barcelona Area.

Tasks and 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.

Opportunities

- 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 CDMO located in Barcelona area, with multiple products/projects ongoing and perspective for market aproval of several products.

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