Quality Assurance Specialist
Job Summary
This role offers the opportunity to play a key part in maintaining and enhancing quality systems within a regulated environment. The ideal candidate will be at the forefront of ensuring compliance, driving continuous improvement, and supporting product development in a dynamic and collaborative setting.
Key Responsibilities
* Maintain and improve quality systems aligned with ISO 13485, ISO 9001, and applicable medical device regulations.
* Develop and revise standard operating procedures (SOPs) and quality documentation.
* Conduct internal audits to ISO 13485 standards.
* Actively participate in customer and regulatory audits.
The successful candidate will work closely with the Quality Team to share knowledge and uphold standards. This is a full-time, permanent, on-site role, Monday to Friday on Days.