I'm looking for...
close

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.

crome
Google Chrome
IE
Internet Explorer
firefox
Mozilla Firefox
opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Contact Info
Jack Caffrey
Life Science

01 507 9279
[email protected]
Connect with me on
Production Team Lead
Dublin South
R&D Engineer
Limerick City
GCP Inspector
Dublin
Controls Engineer
Dublin South
EH&S Specialist
Longford
Process Lead
Donegal
C&Q Engineer
Dublin
Engineering Technician
Dublin South
Clinical Evaluator
Republic of Ireland
NPD Manager
Galway
Engineering Technician
Dublin South
Senior R&D Engineer
Limerick City
R&D Manager
Galway
Global Head of R&D
Republic of Ireland
Process Engineer
Limerick
Project Manager
Kildare
Senior R&D Clinical Engineer
Republic of Ireland
Quality Specialist
Tipperary
R&D Engineer
Dublin
QA Contractor
Dublin City Centre
Project Engineer
Limerick
Controls Engineer
Dublin South
Controls Engineer
Dublin South
Project Engineer
Limerick
Senior CSV Specialist- Hybrid
Republic of Ireland
QC Leader
Cork
Project Engineer
Limerick
Regulatory Affairs Specialist
Republic of Ireland
R&D Manager
Galway
NPD Manager
Galway
R&D Engineer
Galway
NPD Manager
Galway
Design Assurance Engineer
Republic of Ireland
Project Engineer
Limerick
R&D Engineer
Galway
Quality Engineer
Limerick
Engineering Technician
Dublin South
Project Manager
Limerick
R&D Manager
Galway
Head of R&D
Galway
CSV Engineer
Limerick
R&D Manager
Galway
Quality Engineer
Limerick
Apply for this job

Name:

Surname:

Email:

Phone:

Cv:

Salary Expectations:

Education:

Experience:

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]
Details

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.

Responsibilities

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.