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
Sean McCarthy
Life Science

+3530212339371
[email protected]
Connect with me on
R&D Engineer
Galway
Chemical Engineer
Tipperary
Responsible Person (RP)
Republic of Ireland
Project Engineer
Limerick
Project Manager
Limerick
QA Engineer
Leitrim
Project Enginer
Dublin South
Process Engineer
Limerick
R&D Engineer
Galway
Senior Quality Engineer-Remote
Republic of Ireland
Project Engineer
Republic of Ireland
R&D Engineer
Clare
R&D Manager
Galway
Account Manager UK and Ireland
Republic of Ireland
R&D Manager
Connaught
R&D Engineer
Galway
R&D Engineer
Galway
Product Lead
Dublin
R&D Engineer
Dublin
R&D Manager
Galway
QA Manager
Canada
R&D Engineer
Dublin
R&D Engineer
Clare
Project Engineer
Tipperary
Recruitment Consultant
Republic of Ireland
CQV Lead
Tipperary
Medical Device Director
Republic of Ireland
R&D Director
Galway
Manager R&D
Connaught
QA Manager
Canada
R&D Engineer
Galway
R&D Director
Galway
R&D Manager
Galway
Senior Manufacting Engineer
Republic of Ireland
Head of R&D
Galway
R&D Manager
Connaught
Biostatistician
Dublin City Centre
R&D Manager
Connaught
Senior Recruitment Consultant
Republic of Ireland
Senior Recruitment Consultant
Republic of Ireland
R&D Director
Galway
R&D Manager
Connaught
C&Q Lead
Tipperary
Quality Specialist
Tipperary
R&D Manager
Galway
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

Senior Validation Engineer


Reference:SMC4566 Location: Limerick
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Validation Engineer

We’re currently recruiting for an exciting opportunity with an award-winning 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

  • Managing Complexity/Technical Accountability Serves as technical expert for the Validation process and responsibilities to ensure compliance
  • Continuous Learning/Managing Risk Resolves & manages technical operational problems in area of expertise
  • Suggest and sometimes may implement innovation and continuous improvement within the
  • Validation process Implements initiatives in the Validation Process that will deliver customer value at lowest cost.
  • Facilitates successful team behaviour within Quality Systems and across functional areas Manages relationships externally and internally.
  • Builds cross functional and cross-departmental support, fostering overall effectiveness
  • Fosters harmony within Quality Systems.
  • Ensure accuracy and maintenance of the Validation Master List.
  • Review and approve Validation Master Plans, Protocols, Summary
  • Reports and other documentation associated with validations, as appropriate for each validation exercise.
  • Ensure all validation activities and documents are authorised and appropriate compliance approval is gained.
  • Ensure that all validation activities are carried out and reported in a timely manner.
  • Ensure compliance through assisting in audits.

Experience & Education

-A degree level or similar qualification in mechanical or industrial engineering.
-Minimum 2 years experience in a quality role within a regulated industry.
-Proven knowledge and ability regarding product verification and process validations.
-Proven knowledge of FDA and MDD GMP requirements regarding medical devices.