Job Role Overview
A quality laboratory professional is sought by our client to join their Medical Device Regulatory Reporting department. This onsite position offers an initial 12-month contract in Galway.
The successful candidate will be part of a high-performing team responsible for complaint handling and medical device regulatory reporting. They will contribute to the product life cycle through effective within Medical Device Reporting and Vigilance compliance.
Key Responsibilities
* Collaborate with cross-functional teams to build strong relationships and drive business outcomes.
* Coordinate complaint analysis and investigation activities, including receipt and documentation of incoming complaint devices.
* Perform laboratory duties related to complaint analysis and investigation, such as sample preparation and testing.
* Develop and maintain test procedures and non-routine analyses related to root cause investigations.
* Conduct thorough investigations of customer complaints and determine root causes.
* Stay informed about manufacturing processes and final products.
* Maintain laboratory equipment, perform calibration and alignment checks, and ensure instrument maintenance.
Requirements
* Bachelor's Degree in Engineering, Science, or a related field.
* Experience in a medical device or related industry.
* Proven track record in a lab environment.
* Excellent interpersonal, communication, and organizational skills.
* Practical knowledge of statistical data analysis, problem-solving, and quality improvement tools.