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Cure Talent are delighted to be partnered with a medical device manufacturer as they look to strengthen their Quality function. We have an exciting opportunity for a Quality System Engineer to join the team and take ownership of day-to-day quality processes within an established Quality Management System.

As the new Quality System Engineer, you will be responsible for managing and maintaining core quality processes, supporting compliance with ISO 13485 and MDR requirements, and driving continuous improvement across the business. Reporting into the Quality Director, this is a hands-on role with broad exposure across audits, complaints, non-conformances, and GMP activities.

Key Responsibilities

* Manage and maintain the Quality Management System, ensuring ongoing compliance with applicable standards.

* Oversee document control, including release, archiving, and maintenance of controlled documentation.

* Manage non-conformances, supplier corrective actions, and root cause investigations.

* Coordinate customer complaint investigations and generate technical reports as required.

* Oversee internal, external, and supplier audits, ensuring actions are assigned and completed effectively.

* Support deviation management and GMP review of manufacturing and quality records.

* Provide training and quality induction to ensure company-wide understanding of quality procedures.

* Support Management Review and Quality Improvement Review activities with data analysis and reporting.

* Act as deputy for PRRC responsibilities in the absence of the Quality Director.

Experience and Skills Required

* Experience working within a Quality function in the medical device industry.

* Practical experience and training in ISO 13485.

* Degree-qualified in a relevant discipline.

* Knowledge of MDR 2017/745 and FDA 21 CFR Part 820 is advantageous.

* Strong organisational skills, attention to detail, and ability to work cross-functionally.

If you’re a Quality professional looking for a hands-on role focused on QMS ownership, compliance, and continuous improvement within a medical device environment, we’d love to hear from you