Job Overview
This position is responsible for ensuring the quality of medical devices. Key responsibilities include assessing devices, reviewing documentation, and conducting audits to guarantee compliance with regulatory guidelines.
* Audit Procedures: Conduct operational audits and reviews to ensure compliance with applicable procedures and documentation standards.
Qualifications
* Minimum 2 years of related experience in GMP and GDP environments.
* Leaving Certificate or equivalent required.
* Effective communication skills and proficiency in basic computer software.
In this role, you will be working closely with a team to ensure the highest standards are met.