Ubicación: San Sebastián (España)
Jornada laboral: Jornada completa
Sector: Farmacéutico y biotecnología
Vacantes: 1
Disciplina: I+D
Modalidad de trabajo: PresencialViralgen is a CDMO born as a joint venture between AskBio and Columbus Venture Partners created in response to the unmet need for manufacturing of gene therapies. Our goal is to help broaden the access to these life-saving therapeutics and contribute to the advancement of health and human welfare around the world. We want to make gene therapy accessible to all who live with a genetic disease.
We are seeking an experienced and hands-on candidate to join and strengthen our MSAT Drug Product team. In this position, the successful candidate will play a key role in supporting AAV Drug Product formulation and Good Manufacturing Practice (GMP) manufacturing activities.
The responsibilities of this role include working in close collaboration with teams from Research & Development (R&D), production, Quality Control (QC), and Quality Assurance (QA), as well as with external partners. The candidate will be expected to help define robust formulation and process strategies that ensure the quality and consistency of the drug product.
Additionally, the role involves providing support for process scale-up and process validation activities. This is critical for facilitating the transition of products to the late stages of the product life cycle. The candidate will also contribute scientific input on issues related to drug product manufacturability and stability, ensuring that processes remain efficient and compliant with regulatory standards.
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