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Fill & Finish Technician


  • Ubicación: San Sebastián (España)
  • Tipo de Contrato: Temporal
  • Sector: Farmacéutico y biotecnología
  • Vacantes: 1
  • Disciplina: Producción
  • 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

Abour the role
We are looking for a Fill & Finish Technician to join our Manufacturing team and support the production of gene therapy products. In this role, you will perform critical Fill & Finish operations, ensuring compliance with GMP standards, product quality, and production timelines. You will work in a collaborative environment, contributing directly to the delivery of innovative therapies to patients.
 
This is a temporary position.
 
Key tasks

  • Execute Fill & Finish manufacturing activities following GMP requirements and approved procedures.
  • Complete, review, and maintain production documentation accurately.
  • Perform environmental monitoring activities within the manufacturing area.
  • Manage material requirements to support production processes.
  • Identify potential risks affecting product quality, safety, or operations and contribute to solutions.
  • Support production objectives and continuous improvement initiatives.
  • Collaborate with cross-functional teams to ensure successful manufacturing operations.
  • Promote compliance with Health & Safety standards and company policies.

 

Requisitos

Required

  • Professional training in Laboratory Analysis, Quality Control, or a related field.
  • Minimum 3 years of experience in sterile filling operations within the pharmaceutical or biotechnology industry.
  • Experience working in a GMP-regulated manufacturing environment.
  • Strong organizational, planning, and problem-solving skills.
  • Ability to work effectively in a team-oriented environment.
  • Company values: Integrity, Innovation, Collaboration & Accountability.

Nice to have

  • Knowledge of GMP/NCF regulations.
  • Experience in aseptic manufacturing, biologics, or gene therapy production.
  • Continuous improvement mindset and willingness to contribute new ideas.

 

 


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