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

Quality Engineer

Reference:JSC00040702 Location: Galway
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Quality Engineer

We’re currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Galway. 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.


As part of a cross-functional team, provide Quality Engineering input to the product development process and the execution of technology transfer plans.
• Provide on line support during design and/or validation builds with emphasis on production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.
• Provide QE support to qualification and validation activities in conjunction with Engineering and extended QA teams to ensure quality standards are in place.
• Author and support qualification/validation protocols and reports.
• Complete test method validation for methods and procedures used for inspecting, testing and evaluating the precision and accuracy of products, test and production equipment
• Support the introduction/implementation of process/materials/supplier changes to the manufacturing operation. You will assess the impact on process validation for these changes.
• Function effectively as part of cross functional teams; develop strong partnering relationships within these groups and provide constructive feedback and quality leadership.
• Understand product construction, features and uses at a highly competent level to contribute to decision making process on product acceptance standards within their scope of responsibility.
• Support root cause investigations; drive problem solving efforts for quality issues. Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements
• Provide on-going communication, information transfer and record keeping in support of business and core-team objectives and metrics.


• We are looking for a person qualified to Minimum of a Bachelor’s degree (Level 8 NFQ) in a relevant technical discipline (e.g. Engineering, Science) and desirably with a minimum of 2 years relevant experience.
• You are a dynamic team player, can work effectively and proactively on cross-functional teams.
• Initiates and Leads Change, Collaborates and Creates Alignment, Drives Accountability and Thinks Critically and Makes Sound Decisions.
• Knowledge of regulatory requirements and guidelines including 21 CFR parts 210, 211, 21 CFR part 820, ICH requirements and ISO 13485 requirements is an advantage.
• Knowledge of combination products, statistical requirements or software validation requirements is an advantage.
• You are a good communicator and fluent in English, both in writing and speaking.