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Scientist II QC

Oxford Biomedica

Oxford Biomedica

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 Scientist II - QC to join our Quality Control team. In this role, you will perform and report laboratory-based experiments, in accordance with scientific or regulatory requirements , playing a key part in advancing our mission and making a real difference.

Your responsibilities in this role would be:

  • Perform analytical testing as part of QC release and stability.
  • Timely and accurate completion of GxP paperwork.
  • Accountable for own performance in alignment with group objectives and deadlines
  • Flagging process improvement to management
  • Identifying non-conformances (OOS, OOE, CC) and completion under supervision.
  • Will report to the Group Leader or his/her delegated Grade 5 to 6 Scientist.
  • Personally responsible for the completion of tasks in relation to their criticality.
  • Joint responsibility for maintenance and compliance of a GxP laboratory area and GxP “housekeeping” procedures.
  • Work will be conducted in accordance with the OXB Quality Management system.

We are looking for:

  • BSc or equivalent in a relevant Bioscience or basic experience working in a related environment
  • Laboratory technical experience with desirable experience in cell culture, qPCR & molecular biology either within the workplace or study environment.
  • Demonstrate competency in performing laboratory tasks and general experimental procedures.
  • Understanding of laboratory health and safety requirements.
  • Computer Literacy with MS Word, Excel & Outlook & Teams.
  • Some appreciation of Laboratory Information Management Systems (LIMS)
  • Understanding of regulatory requirements e.g. GMP, GLP, GCP and/or Validation and Quality Management systems.
  • Some familiarity with the regulatory requirements for analytical work (e.g. product specifications, stability testing guidelines etc).

About Us:

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

We want you to feel inspired every day. At OXB, we’re future-focused and growing fast. We succeed together—through passion, commitment, and teamwork.

Ready to Make a Difference?

Collaborate. Contribute. Change lives.