Job Overview:
This is an 18-month fixed term position in a hybrid environment. As Quality Engineer, you will work closely with the Senior Quality Engineer and be a key member of the Supplier Quality team.
* You will lead/participate in continuous improvement activities to enhance our quality management system.
* You will perform risk management tasks in a cross-functional setting to ensure compliance with regulatory requirements.
* You will be responsible for ensuring that all documentation and work practices adhere to ISO and regulatory standards.
* You will develop, maintain, and improve our quality management system to meet industry standards.
* You will assess the effectiveness of our quality management system through internal audits and performance reviews.
* You will possess excellent interpersonal skills and be able to work effectively in a team environment.
Requirements:
To be successful in this role, you will need a third-level technical/science qualification and at least two years of experience in the medical device or pharmaceutical industry, preferably within supplier management.
Desirable Qualifications:
A knowledge of quality management systems such as ISO 13485 and GMP would be highly beneficial.