QC Lab Management Analyst

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

Are you passionate about ensuring smooth laboratory operations in a cutting-edge biopharmaceutical environment? Join us as a QC Lab Management Analyst and play a key role in supporting the development and commercial manufacturing of life-changing gene therapy products.

In this position, you will help maintain compliance with Good Manufacturing Practices (GMP), optimize lab resources, and contribute to delivering high-quality products that make a real difference.

This is a temporary role to cover a maternity leave.

Key Tasks:

Oversee and coordinate the availability of laboratory resources, including equipment, reagents, and consumables.
Maintain accurate inventory records and ensure timely procurement of supplies.
Collaborate with the QC team to ensure equipment qualification, calibration, and maintenance.
Coordinate with vendors for equipment servicing and repairs.
Ensure compliance with regulatory guidelines and company quality standards.
Support sample receipt, storage, tracking, and disposal according to protocols.
Participate in internal and external audits.
Work closely with QC analysts, scientists, and cross-functional teams to ensure smooth operations.
Contribute to continuous improvement initiatives and team meetings.

Requisitos

Required

Higher Degree in Quality Control, Laboratory Science, Biotechnology, or a related field.
Strong organizational and planning skills, with the ability to effectively manage priorities and deadlines.
Excellent communication and interpersonal skills, with the ability to collaborate across different teams.
Ability to work in a fast-paced environment and manage multiple activities simultaneously.
Results-oriented mindset with a proactive approach to problem-solving and continuous improvement.
Commitment to Viralgen's values: Integrity, Innovation, Collaboration, and Accountability.

Nice to have

Experience within the biotechnology, biopharmaceutical, pharmaceutical, or advanced therapies industry.
Familiarity with bioanalytical methods and laboratory testing techniques.
Knowledge of GMP regulations and quality standards (GMP)
Exposure to quality systems, regulated laboratory environments, or compliance-driven 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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