A medical device / life sciences organisation is seeking a Quality Systems Engineer to support and maintain key Quality Management System (QMS) processes within a regulated environment.

This role will take ownership of core quality processes including:

• Document Control
• Change Control
• Failure Investigations / Root Cause Analysis

The position works closely with cross-functional teams including Production, Engineering, Regulatory Affairs, R&D, and Supply Chain to ensure compliance with ISO 13485 and FDA quality standards. The successful individual will play a key role in maintaining accurate documentation, supporting audits, driving quality improvements, and ensuring robust investigation processes across manufacturing and operational activities.

Key Responsibilities

• Manage document control activities across the full document lifecycle
• Maintain and administer electronic document manage...