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 [email protected]

Senior Validation Engineer

Reference:SMC2749 Location: Dublin
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 a Pharmaceutical organization based in Dublin. 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.


o Provide expert technical validation support to meet site objectives, comprising of the full validation lifecycles process across a varied equipment portfolio.

o Liaise with engineering, commissioning and qualification personnel, and external vendors regarding equipment qualification and cycle development best practices ensuring quality by design principles are being followed.

o Manage and execute the equipment validation cycle development, performance qualifications and requalification program in line with projects and site validation masterplans.

o Collate and report on relevant validation data and metrics.

o Assist in the development and improvements of the equipment validation and sterilisation lifecycle process while ensuring continued compliance to all applicable regulations. In addition, provide input and guidance into multisite and local procedural requirements.

o Coordinate projects and prioritize workload in line with site priorities.

o Participate, when required, as a member of multidisciplinary site and multisite teams, e.g. cross functional investigation teams, Validation and C&Q network and ISPE network discussions to influence industry best practices.

o Update and maintain validation Standard Operating Procedures (SOPs) in accordance with site and corporate requirements.

o Participate in regulatory inspections, regulatory filings and RTQs

o Attend and contribute to staff meetings and attend appropriate training sessions, as required.

o Comply with the responsibilities as outlined in the Site Safety Statement and champion safe working practices and initiatives within their functional area.

o Perform validation activities using a paperless validation system and identifying opportunities for improvement

Education & Experience

o Bachelor of Science/Engineering degree or equivalent.

o Knowledge of cGMPs and other worldwide regulatory requirements.

o Experience in a similar role

If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or [email protected] for further information.