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
James Cassidy
Life Science

+353 1 5079250
james.cassidy@lifescience.ie
Connect with me on
QC Manager
Dublin
National Sales Representative
Republic of Ireland
R&D Engineer
Dublin
QA Manager
Dublin West
R&D Engineer
Galway
Risk Manager
Dublin
Supply Chain Analyst
Dublin North
API Purchaser
Dublin
Biostatistician
Dublin City Centre
Program Manager
Westmeath
Quality Engineer
Dublin South
QA Manager Biologics
Dublin West
QA Manager
Dublin North
Consultant
Cork
Planner
Dublin
Project Engineer
Dublin North
QA Manager
Dublin
Administration Support
Dublin North
Snr QA Specialist
Dublin South
CTO
Galway
QA Manager
Meath
SAP Planner
Galway
Buyer
Dublin
Quality Assurance Manager
Republic of Ireland
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 applications@lifescience.ie
Details

Regulatory Affairs Graduate


Reference:AFSQ-170870 Location: Westmeath
Qualification:DegreeExperience:Graduate
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Graduate

Regulatory Affairs Graduate
Position will report the Regulatory Affairs Manager. This is a 1 year contract role. Position supports and regulates activities which lead to and maintain compliance.

Responsible

• Assigning and logging of Registration requests for EMEA region
• Preparation of information to support Product Tender Applications and queries in the international markets
• Maintenance of product registration database
• Reconciliation of files and maintenance of files
• Support other activities as required
• Ensure all operations are fully compliant with license details and updated in accordance with relevant guidelines and directives
• Support Regulatory inspections at the site as directed
• Liaise with other departments to ensure correct supporting data generated and provided in a timely manner
• Ensure all operations are fully compliant with license details and updated in accordance with relevant guidelines and directives

Requirements

• Excellent analytical ability
• Excellent technical writing experience within a medical device environment
• The ability to prioritize tasks and be able to manage several projects and tasks simultaneously
• Ability to interface with all levels of management
• Travel up to 30%
• Engineering/Science Degree
• Fluent English, both written and oral
• Problem solving skills for developing creative solutions and meeting objectives are required
• Attention to detail and accuracy
• Skills that enable coordination of data, including MS-Office (primarily PowerPoint, Word, MD Project, Outlook and Excel)


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

James Cassidy | Tel: +353 (0) 1 5079250