Quality Control Scientist (Temporal)

Viralgen; Donostia/San Sebastián; Presencial; EUR 42.000 - 56.000; Jornada completa

Descripción de la vacante

Viralgen is seeking a QC Scientist to join its Quality Control team in Spain. You will ensure reliable analytical testing and support activities aligned with the quality standards across manufactured products, contributing to life-changing gene therapies.

The role emphasizes meeting SOP requirements, maintaining rigorous documentation, and collaborating with the QC team to uphold the company’s quality system and processes.

Formación

• Experience in pharmaceutical QC and analytical testing.
• Familiar with SOPs and quality systems.
• Ability to supervise technicians and ensure timely execution.

Responsabilidades

• Achieve objectives set by the QC Responsible and by Management in a timely manner.
• Organize and supervise the technician activities in the Quality Area, on time and to a high standard.
• Comply with SOPs and deadlines for each analysis and maintain documentation accordingly.
• Collaborate in the maintenance of the company quality system.

Conocimientos

Quality control

Analytical testing

SOP compliance

Team supervision

Descripción del empleo

Are you passionate about pharmaceutical quality control? Join our team as a QC Scientist and contribute to the development and manufacturing of life-changing gene therapies.

You’ll be part of an innovative environment where excellence, collaboration, and continuous learning are at the heart of everything we do.

In this role, your mission will be to ensure reliable analytical testing and related activities within the Quality Control area to guarantee the required quality standards in the manufactured products in our company.

Key Tasks:

• Achieve the objectives set by the QC Responsible and by the Management in a timely manner.
• Organize and supervise the activities carried out by the technician personnel of Quality Area on time and adequate manner.
• Comply and follow with the procedures (SOPs) established for each analysis as well as the requirements and deadlines for their execution.
• Collaborate in the maintenance of the company quality system.