I'm looking for...

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
Contact Info
Sean McCarthy
Life Science

[email protected]
Connect with me on
Quality Engineer
Risk Manager
GMP Inspector
R&D Manager
VP of R&D
Principal R&D Engineer
Dublin Greater
Process Engineer
Clinical Project Manager
Republic of Ireland
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 [email protected]

Process Validation Engineer

Reference:SMC3795 Location: Cork
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 Cork. 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.


1. Ensure validation activities completed comply with US and EU relations, GBSC procedures and EHS requirements.
2. Review and approve documents prepared by project teams, other departments and contractor organizations (e.g. protocols, reports, change controls)
3. Assist in development of validation strategy and validation plan for equipment and process validations.
4. Assist in the development of sampling plans, test plans and data analysis related to process validation.
5. Assist in resolution of deviations/ exceptions during qualification activities
6. Assist with change control activities in accordance with site procedures.
7. Prepare periodic validation review documentation for approval by the business units.
8. Maintain site validation registry.
9. Attend identified training, required to fulfil the role
10. Support the QA Validation team leader in driving improvements within the Validation and Change Control processes to streamline the validation activities associated with Process Changes, Product Transfers and/or New Product Introductions.
11. Participate in cross-functional teams as required.

Education & Experience

• In depth knowledge of 21 CFR 820, 21 CFR 11, ISO 13485 and European regulations associated with the medical device industry