QC Molecular Biology Scientist (Temporal)

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 molecular biology and quality control in the pharmaceutical industry? Join us as a QC Molecular Biology Scientist and contribute to the development and manufacturing of innovative gene therapy products that transform lives.

In this role, you will ensure the accurate execution of molecular biology assays, maintain compliance with Good Manufacturing Practices (GMP), and help deliver high-quality products to patients worldwide.

This is a temporal contract role.

Key Tasks:

Execute and/or review the Molecular Biology assays corresponding to GMP and Toxo batch characterization, raw material testing as well as comparability studies and others.
Participate in the development, qualification and validation of molecular biology methods.
Draft protocols, reports, SOPs, and related documentation for QC activities.
Ensure accurate execution of testing procedures and maintain data integrity.
Report to the QC Molecular Biology Lead any deviation or OOS/OOE/OOT detected.
Manage quality events including root cause investigations.
Analyze, interpret, and evaluate experimental data to ensure method compliance with guidelines, and present results to management or clients.
Collaborate with cross-functional teams to resolve issues and improve QC processes.
Ensure compliance with GMP and regulatory standards.
Identify opportunities for improvement in analytical methodology and laboratory documentation, proposing updates to enhance consistency and regulatory compliance.
Actively contribute to the implementation of digitalization tools and automation systems to drive improvements across the department.

Key Working Relation:

Quality departments
Project management department
Manufacturing department

Requisitos

Skills & Qualifications:

University degree in Biochemistry, Molecular Biology, Biotechnology.
Master or PhD in Biotechnology or related is preferred.
Minimum of 3 years in molecular biology-focused QC roles within pharmaceutical or biotech industries or in a research laboratory environment, developing and executing analytical assays, as well as writing laboratory documentation or scientific papers.
Deep knowledge of molecular biology analytical methods (qPCR, dPCR, sequencing, gel electrophoresis), data analysis and GMP.
Exceptional attention to detail, reliability, and the ability to work in a highly regulated environment.
Excellent problem-solving and analytical skills, with a data-driven approach to decision-making.
Strong communication and interpersonal skills, with the ability to collaborate effectively across functions and teams.
Competent in both written and spoken English.
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.
Achievement of results: direct all actions towards the expected goal.
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, flexibility, etc.

If you’re looking for a role where your work truly matters and you want to grow in a dynamic, forward-thinking company, apply today and help us shape the future of gene therapy!

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

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