QC Lab Management 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 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.

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.
Support material receipt, storage, tracking, and disposal according to protocols.
Collaborate with the Engineering team to ensure equipment qualification, calibration, and maintenance.
Assist in preparing, reviewing, and maintaining FMRGs related to lab operations.
Work closely with QC analysts, scientists, and cross-functional teams to ensure smooth operations.
Ensure compliance with regulatory guidelines and company quality standards.
Participate in internal and external audits.
Contribute to continuous improvement initiatives and team meetings.

Key Working Relation:

Quality departments

Requisitos

Skills & Qualifications:

Education: Higher Degree in Qualiy Control, Laboratory or similar.
Previous experience of 1 year in lab management within the biopharmaceutical 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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