QC Biochemistry Analyst

Ubicación: San Sebastián (España)
Tipo de Contrato: Indefinido
Jornada laboral: Jornada completa
Sector: Farmacéutico y biotecnología
Vacantes: 1
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

Are you passionate about biochemistry and quality in the pharmaceutical industry? Join our team as a QC Biochemistry Analyst 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 accurate execution of biochemical analyses and bioanalytical methods, maintaining compliance with Good Manufacturing Practices (GMP) and helping deliver the highest quality products to patients.

Key Tasks:

Perform biochemical testing following established protocols.
Execute tests for product release and stability studies within defined timelines.
Operate and maintain bioanalytical instruments, ensuring proper calibration and performance.
Analyze data, interpret results, and prepare comprehensive reports.
Collaborate with cross-functional teams to troubleshoot and optimize processes.
Ensure compliance with GMP and regulatory standards.
Contribute to internal and external audits.
Maintain accurate and detailed records of all testing activities.

Key Working Relation:

Quality departments
Manufacturing departments
R&D Departments

Requisitos

Skills & Qualifications:

Education: Bachelor’s degree in Biochemistry, Molecular Biology, Biotechnology, or related field, or Higher Degree in Qualiy Control, Laboratory or similar.
Previous experience of 1-2 years in biochemistry-focused quality control role within the pharmaceutical or biotech industry.

Familiarity with bioanalytical methods for gene therapy products.

Level of English to be able to perform the activities of the department (B2-C1).
GMP: knowledge of NCF/GMP or experience of working on a high regulated industry (recommended)
Organizational and planning skills: set goals and priorities when performing a task, agreeing on the action, deadlines, and resources to be used.
Strategic and improvement vision: encourage a culture of innovation and learning by contributing ideas and continuous improvements
Achivement of results: direct all actions towards the expected goal.
Excellent communication and interpersonal skills, with the ability to work collaboratively across teams.
Ability to work in a fast-paced environment and manage multiple tasks effectively.
Company values: Humility, Empathy, Responsibility, Commitment, Teamwork, and Effort.

We Offer:

A dynamic and collaborative work environment.
Opportunities for professional development and continuous training.
Direct impact on the development of therapies that improve people's lives.
Additional benefits; health insurance, vacation, flexibility, etc.

Ubicación: San Sebastián (España)
Tipo de Contrato: Indefinido
Jornada laboral: Jornada completa
Sector: Farmacéutico y biotecnología
Vacantes: 1
Modalidad de trabajo: Presencial

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