
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 |
![]() Opera |
Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Dublin
Limerick
Galway
Dublin
Galway
Dublin
Cork
Limerick
Dublin
Dublin
Dublin
Westmeath
Westmeath
Dublin
Galway
Limerick
Galway
Dublin
Limerick
Dublin
Cork
Donegal
Galway
Limerick
Limerick
Galway
Dublin
Republic of Ireland
Galway City
Dublin
Cork
Limerick
Galway
Galway
Dublin
Dublin
Louth
Dublin
Carlow
Tipperary
Limerick
Republic of Ireland
Limerick
Carlow
Dublin
Galway
Tipperary
Carlow
Dublin
Tipperary
Limerick
Cork
Galway
Dublin
Limerick
Dublin
Galway
Dublin
Carlow
Dublin
Dublin
Galway
Galway
Galway
Cork
Dublin
Galway
Dublin
Dublin
Tipperary
Louth
Dublin
Westmeath
Cork
Galway
Galway
Dublin South
Galway
Galway
Dublin
Limerick
Galway
Waterford
Limerick
Galway
Galway
Galway
Galway
Republic of Ireland
Carlow
Republic of Ireland
Dublin
Galway
Galway
Cork
Carlow
Cork
Galway
Cork
Limerick
Galway
Tipperary
Dublin
Galway City
Dublin
Limerick
Galway
Wexford
Dublin City Centre
Midlands
Louth
Westmeath
Dublin
Republic of Ireland
Dublin
Tipperary
Limerick
Clare
Dublin
Wexford
Galway
Westmeath
Tipperary
Galway
Dublin
Cavan
Dublin
Dublin
Limerick
Galway
Cavan
Dublin
Tipperary
Senior Validation Engineer
Reference: | SMC38597 | Location: |
Limerick |
Qualification: | Degree | Experience: | See description |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
We’re currently recruiting for an exciting opportunity with a Medical Device organization based in Limerick. 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.
Duties
− Responsible for supporting the activities of Operations / Engineering / Information Management in building product Quality into our products and assuring compliance to the pertinent regulations while at the same time attaining operational effectiveness
− Work with the various departments/groups in development and execution of validation activities associated with new equipment/product or I.M. system upgrades
− Runs /Manages complaint investigation and resolution of same
− Designs and develops validation documentation to support business continuity, new process/product introductions and process improvement requirements
− Implementation and co-ordination of the change control process promotes timely approval of all supporting documentation
− All employees are responsible for minimising both the Environmental and Health & Safety effects of the work that they perform.
Education & Experience
− Be very familiar with the relevant regulatory standards (F.D.A. - Quality System regulations, ISO 13485) applicable to the manufacture of Class III medical devices to Global markets.
If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or [email protected] for further information.
Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
Valid XHTML - CSS






