Senior QA Officer
Oxford Biomedica
Quality Assurance
England, UK
Posted on Mar 25, 2026
Location:
Oxford, GB
Company: oxfordbiom
Join us in changing lives.
At OXB, our people are at the heart of everything we do. We’re on a mission to enable life-changing therapies to reach patients around the world—and we’re looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful
We’re currently recruiting for a Senior Quality Assurance Officer to join our Quality Assurance team. In this role, you will provide expert QA support for OXB Manufacturing Operations, playing a key part in advancing our mission and making a real difference.
Your responsibilities in this role would be:
OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies.
OXB collaborates with some of the world’s most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXB’s world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.
Why Join Us?
Ready to Make a Difference?
Collaborate. Contribute. Change lives.
Oxford, GB
Company: oxfordbiom
Join us in changing lives.
At OXB, our people are at the heart of everything we do. We’re on a mission to enable life-changing therapies to reach patients around the world—and we’re looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful
We’re currently recruiting for a Senior Quality Assurance Officer to join our Quality Assurance team. In this role, you will provide expert QA support for OXB Manufacturing Operations, playing a key part in advancing our mission and making a real difference.
Your responsibilities in this role would be:
- Reviewing and approving deviations, CAPAs and change controls within defined timelines.
- Supporting manufacturing teams as a QA partner to ensure GMP compliance during production activities.
- Reviewing batch documentation and support preparation for Qualified Person batch disposition.
- Participating in investigations, root cause analysis and risk assessments for quality events.
- Reviewing and approving SOPs, protocols, reports and other GMP documentation.
- Supporting implementation of new manufacturing processes for incoming client programs.
- Contributing to continuous improvement initiatives to strengthen quality systems and operational processes.
- Experience in a GMP-regulated pharmaceutical, biotechnology or similar manufacturing environment.
- Significant experience managing quality events such as deviations, CAPAs and change controls.
- Strong understanding of GMP regulations and regulatory expectations (FDA / EMA).
- Ability to work independently, make sound quality decisions and manage multiple priorities.
- Strong communication skills and the ability to collaborate closely with manufacturing and technical teams.
OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies.
OXB collaborates with some of the world’s most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXB’s world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.
Why Join Us?
- 💸 Competitive total reward packages
- 🧘 Wellbeing programmes that support your mental and physical health
- 🚀 Career development opportunities to help you grow and thrive
- 🤝 Supportive, inclusive, and collaborative culture
- 🧪 State-of-the-art labs and manufacturing facilities
- 🌍 A company that lives its values: Responsible, Responsive, Resilient, Respect
Ready to Make a Difference?
Collaborate. Contribute. Change lives.
