Quality Assurance Professional
A key role has arisen for a multinational medical device organization based in Galway. The position involves working within a high-performing complaint handling and medical device regulatory reporting department.
Key Responsibilities:
* Collaborate with cross-functional teams to build effective relationships with external suppliers and regulatory bodies.
* Oversee complaint handling analysis and investigation activities, ensuring prompt and efficient resolution.
* Perform laboratory tasks related to complaint analysis and investigation, utilizing expertise in relevant areas.
* Contribute to the development of test procedures and non-routine analyses, driving process improvement.
* Coordinate customer complaint investigations, maintaining open communication with stakeholders.
* Foster an awareness of the manufacturing process and final products, ensuring alignment with quality standards.
* Provide laboratory support functions, perform instrument maintenance, calibration, and alignment checks.