R&D Quality Systems Administrator – On-site

CooperVision; Southampton; On-site; GBP 32,000 - 46,000; Full time

Benefits offered by this job

Holiday

Pension scheme

Healthcare cover

Life assurance

Wellness platform

Discounted contact lenses

Job summary

CooperVision, a leading global contact lens manufacturer, seeks a Quality Systems Administrator in the UK R&D QA team. Based at The Vision Centre, Southampton, you will support the UK QMS and global initiatives, ensuring quality and regulatory compliance.

You will monitor processes, coordinate change control, and assist with audits and CAPA activities, contributing to continuous improvement within a fast-paced med‑device environment. On-site role with strong development opportunities.

Qualifications

• Knowledge of quality systems in medical device manufacturing.
• Excellent written and verbal communication.
• Strong organisational skills and attention to detail.
• Experience with QA processes and audits is desirable.
• Ability to read and understand technical material.
• Experience with documentation and change control.

Responsibilities

• Monitor and improve areas of the Quality System and promote QA compliance.
• Oversee Document Change Control and approvals; assign document numbers.
• Review and approve Batch Records for GMP/GDP compliance.
• Support CAPA and NCR investigations and closure.
• Assist with CAPA investigations, implementation and effectiveness reviews.
• Support audits (internal, supplier and regulatory) and associated corrective actions.

Skills

Quality systems

Communication

Organisational skills

Technical reading

Teamwork

Prioritisation

Attention to detail

Fast-paced work

Education

Bachelor's degree

Tools

Word

Excel

Outlook

Relational databases

Job description

CooperVision, a leading global contact lens manufacturer, seeks a Quality Systems Administrator in the UK R&D QA team. Based at The Vision Centre, Southampton, you will support the UK QMS and global initiatives, ensuring quality and regulatory compliance.

You will monitor processes, coordinate change control, and assist with audits and CAPA activities, contributing to continuous improvement within a fast-paced med‑device environment. On-site role with strong development opportunities.