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
Jack Caffrey
Life Science

01 507 9279
[email protected]
Connect with me on
Quality Engineer
Limerick
Process Engineer
Limerick
QC Scientist
Limerick
Process Engineer
Dublin North
Validation Lead
Limerick
R&D Manager
Galway
Head of R&D
Galway
Project Engineer
Limerick
Technical Writer
Limerick
Senior R&D Engineer
Limerick City
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

Associate Quality Engineer


Reference:JSC00034146 Location: Galway City
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: QE Manufacturing Engineer

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

Duties

At our Sterilization Validation Services Department, we focus on product quality excellence and providing exemplary service to the business units we support. Our Quality Engineers are directly involved in building the organization in support of Sterility Assurance for New Product Development and Site Transfers.

• Support sterility assurance activities for new products and change control, developing strong partnering relationships with these groups, at both manufacturing and design sites
• Participate in root cause investigations and continuous improvement in day-to-day activity, initiating appropriate corrective actions and following through to implementation
• Support EuMDR project work for Sterilisation Validation team
• Support cross functional teams in design protocols to ensure that new products/ product changes are adequately evaluated/tested to guarantee compliance to all regulatory standards.
• Deliver on projects assigned and works with other stakeholders to achieve desired results within defined timeframes
• Support your projects in internal and external audits and in submission preparation, addressing any questions regarding these submissions
• Performs calculations, technical and record keeping duties in conformance with company and regulatory policies and standards to meet quality and accuracy requirements.
• Adheres to all relevant site wide procedures and practices for Safety & GMP


Education & Experience


• Degree (Level 8) qualification in relevant technical discipline e.g Science or Engineering
• 2 years’ experience with Sterilisation Validation or Biocompatibility is desirable
• Excellent understanding of GMP and documentation required
• Dynamic team player with good communication skills
• Can work effectively and proactively as an individual or on cross functional team.