QA Technician
Listed on 2026-08-03
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Quality Assurance - QA/QC
Data Analyst, Regulatory Compliance Specialist
Viralgen is a CDMO born as a joint venture between Ask Bio 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 wanttomake genetherapyaccessible to allwho live with agenetic disease.
Aboutthe role
We are looking for a Quality Assurance Technician to join our QA Operations team and help ensure that our quality systems and manufacturing activities meet the highest GMP standards.
This role is ideal for someone who enjoys working in a highly regulated environment, collaborating across teams, and contributing to the delivery of innovative gene therapies through strong quality oversight and continuous improvement.
This is a temporary position.
Key tasks- Support the maintenance and continuous improvement of the Quality Management System.
- Review quality documentation and GMP batch records to ensure compliance and data integrity.
- Manage quality events, deviations, complaints, change controls, and CAPAs.
- Collaborate with Manufacturing, QC, and other departments to resolve quality-related issues.
- Support GMP training initiatives and promote quality best practices across the organization.
- Participate in audits, inspections, and ongoing quality improvement projects.
- Degree in Pharmacy, Biotechnology, Biology, Chemistry, Biochemistry, Engineering, or a related scientific discipline.
- Experience in Quality Assurance, Quality Systems, or GMP-regulated environments.
- Strong organizational skills and attention to detail.
- Excellent communication and problem-solving abilities.
- Ability to work effectively with cross-functional teams.
- Copmany values:
Integrity, Innovation, Collaboration & Accountability.
- Experience with in the biotechnology, pharmaceutical, or advanced therapies industry.
- Knowledge of GMP requirements and quality management systems.
- Exposure to audits, CAPAs, deviations, and change control processes.
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