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

Validation Engineer

Reference:KGAIIC-750044 Location: Galway
Galway City
Qualification:DegreeExperience:2-3 Years
Job Type:PermanentSalary: Not Disclosed

This company provides access to high quality medicines for millions of people worldwide.

Make a Difference
Each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here's how this role will help:

• Responsible for writing, executing & reporting of all validation activities including but not limited to (VP/ DQ / FAT / IQ / OQ / PQ / PPQ / pFMEA).
• Validation/Qualification projects will be across a range of production areas which may include, Equipment Qualification (Lyophilisers, Autoclaves, Filling Lines etc), Product Processes, Cleaning, Computerised Systems, Utilities and associated Capital projects.
• Act as a subject matter expert in process validation which will be performed against Corporate SOP/HPRA /FDA/EMEA requirements.
• Generation, execution and close out of validation projects relating to existing products and new product introductions.
• Participates in project teams and assists in determining project schedules and the relevance of appropriate levels of validation.
• Statistical analysis of data to determine process capability.
• Execution and documenting of process risk assessment / failure mode and effects analysis.
• Track and resolve exceptions during qualification activities.
• Represent validation at internal and external audit.

Make Our Values Your Values
Our client hires only the best. People who thrive in a culture of innovation and empowerment. People who are active learners and have a positive attitude. People who are leaders and know that by working together we can run faster, reach higher and achieve more. By doing so, we will continue to set new standards in health care. Here are the minimum qualifications and essential functions for this position:

• Minimum of a Diploma in a Science/ Engineering or related discipline and 2-4 years’ experience in a Technical/QA/ Validation Role within the pharmaceutical industry or a similar operating environment with in-depth knowledge of validation processes.
• Experience in statistical analysis techniques and process validation will be considered a distinct advantage.
• Must process knowledge of Pharmaceutical Manufacturing Programs
• Must possess strong project management and organizational skills. Self-motivation and drive.
• Excellent interpersonal, communication (written & oral) & technical report writing skills.
• Must be flexible and able to manage multiple priorities simultaneously.
• Must be an active learner and have a positive leadership attitude.
• Proficiency in speaking, comprehending, reading and writing English is required.

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

Kevin Silke | Tel: +353 (0) 1 507 9255