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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