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

Quality, Compliance and Regulatory Affairs Coordinator

Reference:AWPX-834277 Location: Dublin
Qualification:DegreeExperience:2-3 Years
Job Type:PermanentSalary: Not Disclosed

Quality, Compliance and Regulatory Affairs Coordinator

Our client, one of the leading medical device distributors across Ireland and U.K are recruiting for QCRA Coordinator who will reporting to the QCRA Manager will the Quality, Compliance and Regulatory Affairs requirements. The successful candidate will manage the ongoing maintenance of our compliance requirements ensuring we meet and exceed our contractual and regulatory obligations, providing best practice in QMS.

The Position

·Support the Quality Manager in relation to the maintenance of our ISO Quality Management System
·Assist in carrying out of Internal Audits to ISO 9001:2015 standard
·Issue and Track non-conformances and CAPAs
·Document Control – version control for SOPs, index register, go live and communication
·Monthly checks for quarantine, calibration and temperature monitoring
·Recording and monitoring of classification of products and identification of any registration or licensing requirements through our Vendor Approval Process
·Management of Quality page and updates to all employees
·Administration of training completion in conjunction with Human Resources
·Processing of requests for Educational Support
·Manage requests for JCI information from customers and liaise with relevant internal departments
·Follow the product complaint reporting process from reporting to close out, liaising with the product manufacturer and internal stakeholders
·Preparation of Monthly reporting of open complaints to QCRA Senior Management, driving complaints to closure with responsible parties
·Follow Field Action process from receipt of Field Action from the manufacturer through to close out with patient safety as our number one priority.
·Responsible for the introduction of new /amended SOPs into QMS working closely with the Projects Department

The Person

·Third level qualification required in Quality, Science, or Business
·2-3 years Administrative experience essential
·Strong communication, interpersonal and prioritising skills
·Good time management
·Keen attention to detail
·Good planning & organizing skills
·A good work ethic with a positive, can do attitude and approach to work
·Ability to work on their own initiative and equally as part of a team
·Full Clean Driving License required
·Strives for Continuous Improvement

If you would like further Information you can contact the recruiter directly:

Jannet Diana | Tel: +353 (0) 1 507 9255


Under the Data Protection Acts 1988 and 2003, your details will be kept confidential and will not be passed to a third party without your express prior consent.

Twitter | Linkedin

Science Recruitment | Engineering Jobs | Scientific Jobs

Pharmaceutical Jobs | Medical Device Jobs | Clinical Research Jobs | Biotechnology Jobs