Manufacturing Quality Engineer

Description

Cure Talent are delighted to partner with a leading organisation in the medical device industry in their search for a Manufacturing Quality Engineer to join their expanding team.

As the new Manufacturing Quality Engineer, you will be responsible for maintaining validation, process control, and documentation in compliance with QMS requirements. The role will also involve overseeing documentation control, and writing full end to end documentation, including validation protocols, reports, and standard operating procedures.

Responsibilities

Lead and support equipment and process validation, including preparing protocols, conducting testing, and generating reports

Write, review, and approve full end–to–end documentation, including SOPs, work instructions, risk assessments, and validation reports.

Investigate and resolve manufacturing issues impacting product quality.

Identify and drive process improvements to enhance quality, efficiency, and compliance.

Monitor process capability and equipment performance through data analysis, identifying trends and opportunities for improvement.

Key Requirements

Proven experience in a Manufacturing, Process, Validation or Quality Engineering role within a regulated manufacturing environment.

Strong understanding of process and equipment validation, including documentation and reporting.

Demonstrable ability to create and maintain high–quality documentation with excellent attention to detail.

Strong communication skills with the ability to influence and collaborate across departments.

If you are a proactive Manufacturing Quality Engineer who thrives in a regulated environment, we would be delighted to hear from you.

Ad ID: 5417371028