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.
Responsibilities
- Ensure that the different operational activities are performed in a timely manner and in accordance with Good Manufacturing Practices and Applicable Guidelines.
- Support process optimizations implemented in the facilities, services and equipment according to the data and recommendations of the scientific/production team.
- Collaborate in the achievement of production objectives set by the company in a timely manner.
- Manage cleaning materials and activities.
- Manage the necessary wardrobe according to the needs of the company.
- Ensure that the different production areas have the necessary raw materials to carry out production.
- Manage a support team for the different production rooms, preparing and sterilizing material.
- Supervise the performance of filter tests.
- Supervise the fractioning required for the different productions.
- Execute the planning stages as part of the production process.
- Assess, communicate and mitigate key manufacturing risks and/or operational obstacles.
About you
- Advanced training in Quality Control, Laboratory, Anatomic Pathology, or similar.
- Knowledge in GMP.
- Intermediate/advanced level of English.
- Ability to work in a team.
- Teamwork skills.
- Commitment and confidentiality.