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.
AsthenewManufacturingQualityEngineer,youwill 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
1. Proven experience in a Manufactur...