QC System Administration Scientist

Ubicación: San Sebastián (España)
Sector: Farmacéutico y biotecnología
Vacantes: 1
Disciplina: Calidad
Modalidad de trabajo: Híbrida

Viralgen Vector Core, S.L.U.

Viralgen 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.

Descripción de la oferta

About the role

We are looking for a QC System Administration Scientist to join our Quality Control team and help ensure the effective management of QC systems, documentation, and laboratory processes within a GMP environment.
This role offers the opportunity to work at the intersection of quality, science, and digitalization, supporting key activities such as batch release, stability studies, LIMS management, and continuous improvement initiatives that contribute to the delivery of advanced gene therapies.

Key Tasks

Manage QC documentation and system-related activities supporting GMP operations.
Coordinate stability studies, specifications, and sampling plans.
Support batch release activities through the review of QC data and documentation.
Generate and review quality records, reports, and certificates.
Contribute to the administration and continuous improvement of LIMS and other digital quality tools.
Collaborate with QC laboratories and cross-functional teams to ensure efficient execution of projects and studies.
Support quality system activities, including non-conformities, change controls, and CAPAs.
Drive process improvements to enhance compliance, efficiency, and data integrity.

Requisitos

Required

Degree in Biotechnology, Molecular Biology, Biochemistry, or a related scientific field.
Experience in Quality Control, Quality Systems, or GMP-regulated environments.
English level B2/C1.
Strong organizational skills and attention to detail.
Ability to manage multiple priorities and collaborate with different stakeholders.
Excellent problem-solving and analytical thinking skills.

Nice to have

Experience within the biotechnology, pharmaceutical, or advanced therapies industry.
Knowledge of GMP requirements and laboratory quality systems.
Experience with LIMS or laboratory digitalization projects.

Ubicación: San Sebastián (España)
Sector: Farmacéutico y biotecnología
Vacantes: 1
Disciplina: Calidad
Modalidad de trabajo: Híbrida

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