Quality Systems Specialist - GMP, Audits & CSV

OXB; Oxford; On-site; GBP 35,000 - 45,000; Full time

Job summary

A leading viral vector CDMO in Oxford is seeking a Quality Systems Officer responsible for maintaining Quality Management Systems and promoting continuous improvements. Ideal candidates should have A-Level education (preferably in science), experience in a GMP environment, and knowledge of pharmaceutical regulations. The role involves supporting quality systems, conducting audits, and delivering training. Competitive compensation and supportive culture are offered.

Benefits

Competitive total reward packages

Wellbeing programmes

Career development opportunities

Supportive and inclusive culture

Qualifications

• A-Level education in science preferred or equivalent experience.
• Experience working within a GMP-regulated environment is required.
• Knowledge of pharmaceutical regulations and compliance is essential.

Responsibilities

• Provide primary Quality Systems support for suppliers and services.
• Maintain internal audit schedules and contribute to Quality Reports.
• Deliver training on Quality Management Systems.

Skills

Experience working within a GMP-regulated environment

Knowledge of pharmaceutical regulations and compliance requirements

Proficient in Microsoft Office (Word, Excel, Outlook, PowerPoint)

Education

A-Level education in science or equivalent experience

Tools

Electronic Quality Management Systems (eQMS)

Job description

A leading viral vector CDMO in Oxford is seeking a Quality Systems Officer responsible for maintaining Quality Management Systems and promoting continuous improvements. Ideal candidates should have A-Level education (preferably in science), experience in a GMP environment, and knowledge of pharmaceutical regulations. The role involves supporting quality systems, conducting audits, and delivering training. Competitive compensation and supportive culture are offered.