Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

Google Chrome
Internet Explorer
Mozilla Firefox

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job






Salary Expectations:



Current Location:

Notice Period:

Write here your cover note:

If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to [email protected]

Assoc MDR/Vigilance Specialist

Reference:JSC0007388 Location: Galway
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Sales And Marketing Manager

We’re currently recruiting for an exciting opportunity with an award-winning medical device organization based in Galway. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

You will be part of a high performing Complaint Handling and Medical Device Regulatory reporting department, which provides value throughout the Product Life cycle through world class execution in Medical Device Reporting and Vigilance compliance.


Responsible for the co-ordination of complaint handling activities for a wide range of products.

Responsible for the receipt and documenting of incoming complaint events. Responsible for co-ordination of cross functional activities in the investigation of customer complaints and determination of root cause.

Ensures complete and accurate maintenance and reporting of Medical Device Reports (MDRs) as required by regulatory agencies.

Support the response to any queries received from regulatory agencies in relation to complaint events or post market regulatory reports.

Support risk management, risk analysis and health hazard analysis associated with complaint/ post market information.

Contribute to continuous improvement activities to support the role out of cell operating systems and pronciples within the CQXM department.

Key skills and experience:

Qualified person to bachelor's degree (Level 8 NFQ) in Engineering/ Science or related discipline.

Candidates with a legal or clinical qualification (e.g. registered nurse or experience in physiological or clinical measurement science) will also be considered. 1-2 years relevant experience in a medical devices or related environment.

Dynamic team player who can work effectively and proactively on cross functional teams. Ability to think critically and make sound decisions.

Must be focused on patient safety and customer service, set high standards, instils operational excellence, drive accountability and model ethical behaviour.

Good communicator and fluent in English, both in writing and speaking.