Quality Control Technical Specialist

Quality Control Technical Specialist - OXB

Location:

Oxford, GB

Company: oxfordbiom

We’re on a mission to enable life‑changing therapies to reach patients around the world. We’re looking for passionate individuals who embody our core values every day:
Responsible, Responsive, Resilient, and Respectful
.

In this role, you will be a technical Subject Matter Expert for the ADQC Team, leading activities to ensure quality standards are met and ensuring delivery to meet manufacturing needs and wider business requirements. This is an onsite opportunity.

• Represent the company in communications with external testing laboratories and suppliers ensuring test results and quality information is provided.
• Create and review all types of quality records in OXB's QMS system.
• Highlight any non‑conformances and recurring issues.
• Assist in the compilation of trend data, setting limits and reporting from batch testing.
• Write technical protocols and reports, analyze data and draw conclusions.
• Review, suggest and implement appropriate updates to SOPs and policies.
• Perform investigations, utilising RCA tools and suggesting suitable CAPA.
• Input into the organisation and planning of the workload to generate a daily/weekly schedule of work.

• Life Science graduate with experience working within a pharmaceutical regulated environment.
• Strong knowledge of GMP regulations.
• Knowledge of Quality Management Systems.
• Highly skilled in the use of MS Office (Excel, Word, PowerPoint, Outlook).
• Proven skills in critical thinking and troubleshooting.

OXB is a quality and innovation‑led viral vector CDMO with more than 30 years of experience. We collaborate with innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno‑associated virus (AAV) and adenoviral vectors. Our world‑class capabilities span early‑stage development to commercialisation and are supported by robust quality‑assurance systems, analytical methods, and deep regulatory expertise.

• Competitive total reward packages.
• Wellbeing programmes that support your mental and physical health.
• Career development opportunities.
• 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.

Entry level

Full‑time

Quality Assurance

Pharmaceutical Manufacturing