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

Regulatory Affairs Specialist

Reference:KG-ARVS-733434 Location: Galway
Qualification:DegreeExperience:2-3 Years
Job Type:PermanentSalary: Not Disclosed

This job requires the person to work within the current regulatory environment and frameworks for all relevant markets. You will support marketing the products and ensure they are in conjunction with the commercial requirements.

• Define regulatory strategy for individual devices within the Product Development Process.
• As appropriate, manage Submissions and Significant Changes and Notified Body interactions.
• Assist with the preparation of egulatory filings and subsequent FDA correspondence on submissions.
• Manage Regulatory Assessment of any Device and Quality System changes, and any subsequent notifications that are required to be made to Regulatory Agencies.
• Work with the Commercial Team and Distributors, to ensure country specific registration activities are understood and appropriately addressed.
• Participate in Notified Body, and Regulatory Agency audit preparation.

• A minimum of a Degree (Hons) in Quality/Regulatory or related discipline
• At least 3 years practical and relevant experience in Regulatory Affairs, medical device preferable.
• Excellent verbal and written communication skills.
• Excellent attention to detail skills.
•Good understanding of ISO and FDA quality standards.

Environmental Conditions:
• Typical office environments, with work also performed in R&D and manufacturing labs, and customer/supplier locations.

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

Kevin Silke | Tel: +353 (0) 1 507 9255