Analyst II, Quality Control, Chemistry

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.

Following the expansion of our US footprint with the acquisition of a new commercial-scale viral vector facility in Durham, North Carolina we have some new opportunities to join us.

We’re currently recruiting for a Quality Control Analyst II to join our Quality Control team. In this role, you will support routine QC Chemistry testing of GMP gene therapy and gene editing products for the GMP clinical manufacturing facility and for clients, playing a key part in advancing our mission and making a real difference.

Your responsibilities in this role would be:

• Perform routine QC testing including, but not limited to: HPLC, UPLC, LCMS, CE, and AUC
• Perform instrument setup, troubleshooting, and data analysis to ensure high-quality results.
• Support analytical method qualification, validation, and method transfer activities.
• Authors and Revises SOPs/Forms and other relevant controlled documentation
• Performs peer review of both internal and externally generated data
• Supports routine laboratory operations (equipment cleaning, laboratory cleaning, inventory control, logbook management)
• Ensures laboratory operational readiness and assists with troubleshooting/continuous improvement as needed
• Ensures all tasks are performed in a manner consistent with safety standards

We are Looking For:

• Bachelor’s or master’s degree in biology, Chemistry or equivalent
• Minimum 3 years of experience in the biotech industry
• Experience in HPLC, CE and Compendial analyses
• Hands on experience with LCMS testing a plus
• Experience with OOS, deviations, CAPAs, change controls and risk assessments
• Experience with data review and presenting results to functional management
• Hands on experience in cGMP environment

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.

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 25 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 programs 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?