Quality Control Scientist (Temporal)

Location: San Sebastián (Spain)
Contract: Temporary
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Work modality: On site

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.

Job description

Are you passionate about pharmaceutical quality control? Join our team as a QC Scientist 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 reliable analytical testing and related activities within the Quality Control area to guarantee the required quality standards in the manufactured products in our company.

Key Tasks:

Achieve the objectives set by the QC Responsible and by the Management in a timely manner.
Organize and supervise the activities carried out by the technician personnel of Quality Area on time and adequate manner.
Comply and follow with the procedures (SOPs) established for each analysis as well as the requirements and deadlines for their execution.
Collaborate in the maintenance of the company quality system.
Maintain a good working environment

Key Working Relationships:

Quality departments
Manufacturing departments
R&D departments

Requirements

Professional education in quality control and pharmaceutical products or University degree in Biochemistry, Molecular Biology, Biotechnology or another related field.
Master’s degree in Analytical areas and/or Quality Systems in the Pharmaceutical Industry or PhD in Biology, Biochemistry, Biotechnology or another related field will be positively assessed.
Previous work experience of at least 2 years is required in similar analytical positions.
Fluent Spanish and English, oral and written
Computer skills: advanced user level of the Office package. Knowledge with Bioinformatic analysis softwares will be positively assessed
GMP: Knowledge of GMP requirements or experience working in a highly regulated industry is desirable.
Organizational and planning skills: Ability to set goals and priorities when performing a task, defining the actions, deadlines, and resources required.

Continuous improvement mindset: Ability to promote a culture of innovation and learning by contributing ideas and continuous improvements.

Results orientation: Ability to direct all actions towards achieving the expected outcomes.
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.
Alignment with company values: Integrity, Innovation, Collaboration, and Accountability.

Location: San Sebastián (Spain)
Contract: Temporary
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Work modality: On site

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