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
Senior Chemist
Dublin North
R&D Engineer
Program Manager
QA Manager
Snr QA Specialist
Dublin South
QA Manager Biologics
Dublin West
Market Access Manager
Dublin City Centre
CEO Medical Device Start Up
Republic of Ireland
Qualified Person
Dublin West
Principal Scientist
Dublin South
QA Manager
Dublin West
Head of Quality
Dublin West
Snr Process Engineer
Dublin North
QA Specialist
Dublin West
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 applications@lifescience.ie

Quality Engineer

Reference:CC/HQ00001860 Location: Dublin
Qualification:DegreeExperience:4-5 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: EHS Engineer, Quality Engineer


Our multinational client in South Dublin requires a Quality Engineer. Reporting to the Senior Quality Engineer duties will include management and execution of process validation studies, active participation in non-conformance investigation, process improvement projects, project management, application of SPC to current production processes and liaison with key customers.

• Be a key driver of cGMP practices within Operations and Quality divisions
• Provide support for the ISO9001/2000 and ISO13485 and 21CFR Part 820 Quality Systems
• Become an active member of the site internal audit team, liaising with Regulatory auditors
• Prepare and maintain documentation in compliance with the appropriate regulatory requirements
• Support production personnel in relevant continuous improvement activities (Six Sigma etc.)
• Act as customer liaison contact for given key customers as appropriate.
• Review, analyse and report on relevant customer complaints.

• A primary degree in a Science/Engineering discipline (Preferably Polymer Science/Engineering or Mechanical Engineering)
• A minimum of 5 years work experience in an ISO 9001/2000 or ISO 13485 environment, coupled with a background in Medical Devices/Pharmaceutical Industry.
• Experience in the preparation of Technical Documentation.
• Knowledge of Statistical Process Control and Six Sigma methodologies (Greenbelt Certification would be advantageous).
• Experience in CAPA system management
• A working knowledge of FDA requirements and managing FDA audits.
• Experience in process validation and working in a clean room environment.
• Proven ability of working in a cross-functional team environment.
• Excellent interpersonal and communication skills and high level of computer literacy.

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

Conor Cronin | Tel: +353 (0) 1 5079258