Quality Assurance & Document Controller

Industry: Life Sciences / Medical Devices
Location: Surrey

Join a leading organisation in the life sciences sector as a Quality Assurance & Document Controller, supporting and enhancing a multi‑site Quality Management System. This role is ideal for someone who enjoys variety, autonomy, and working within a regulated, high‑impact environment.

Key Responsibilities

• Conduct internal audits across multiple manufacturing sites.
• Host customer audits and support external certification audits (ISO 9001 & ISO 13485).
• Manage document control, change control, and contribute to product/batch release processes.
• Monitor quality metrics and report findings to leadership.
• Collaborate with engineering, manufacturing, and global quality teams to drive continuous improvement.

What You'll Bring

• 2+ years' experience in Quality Assurance within life sciences, medical devices, or a regulated environment.
• Strong knowledge of QMS principles and audit processes.
• Experience with document control and compliance standards (e.g., ISO 14971, ISO 62304, GMP/GxP).
• Excellent communication, organisation, and problem‑solving skills.
• Degree in Life Sciences, Engineering, Chemistry, Business, or related field (Lead Auditor certification desirable).

Why Apply?

• Opportunity to shape and elevate quality processes across multiple sites.
• Exposure to global teams and industry‑leading standards.
• A role with autonomy, impact, and clear development potential.