QA Technician

Ubicación: San Sebastián (España)
Tipo de Contrato: Temporal
Sector: Farmacéutico y biotecnología
Vacantes: 1
Disciplina: Calidad
Modalidad de trabajo: Presencial

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 Quality Assurance Technician to join our QA Operations team and help ensure that our quality systems and manufacturing activities meet the highest GMP standards.

This role is ideal for someone who enjoys working in a highly regulated environment, collaborating across teams, and contributing to the delivery of innovative gene therapies through strong quality oversight and continuous improvement.

This is a temporary position.

Key tasks

Support the maintenance and continuous improvement of the Quality Management System.
Review quality documentation and GMP batch records to ensure compliance and data integrity.
Manage quality events, deviations, complaints, change controls, and CAPAs.
Collaborate with Manufacturing, QC, and other departments to resolve quality-related issues.
Support GMP training initiatives and promote quality best practices across the organization.
Participate in audits, inspections, and ongoing quality improvement projects.

Requisitos

Required

Degree in Pharmacy, Biotechnology, Biology, Chemistry, Biochemistry, Engineering, or a related scientific discipline.
Experience in Quality Assurance, Quality Systems, or GMP-regulated environments.
Strong organizational skills and attention to detail.
Excellent communication and problem-solving abilities.
Ability to work effectively with cross-functional teams.
Copmany values: Integrity, Innovation, Collaboration & Accountability.

Nice to have

Experience within the biotechnology, pharmaceutical, or advanced therapies industry.
Knowledge of GMP requirements and quality management systems.
Exposure to audits, CAPAs, deviations, and change control processes.

Ubicación: San Sebastián (España)
Tipo de Contrato: Temporal
Sector: Farmacéutico y biotecnología
Vacantes: 1
Disciplina: Calidad
Modalidad de trabajo: Presencial

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