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
James Cassidy
Life Science

+353 1 5079250
Connect with me on
Automation Technician
Dublin South
API Purchaser
Supply Chain Analyst
Dublin North
R&D Engineer
Administration Support
Dublin North
Dublin City Centre
Program Manager
QC Manager
Senior Buyer
R&D Engineer
QA Manager Biologics
Dublin West
QA Manager
Dublin West
QA Manager
Snr QA Specialist
Dublin South
QA Manager
Dublin North
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

Manufacturing Engineer

Reference:JC/HQ00001643 Location: Galway
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed

Manufacturing Engineer

Our client a start-up medical device company based in Galway is currently seeking a Manufacturing Engineer to join their team. Reporting to Operations Engineer the manufacturing engineer will be responsible for the identification and implementation of manufacturing process improvements and to complete assigned work in a manner which complies with the company’s Quality Management System. Client ismoving into operation stage with product require someone to work on scale up of product and act as point of contact with venbdors and third partner manufacturers. Can look at Senior and/or Engineer level


Identification and implementation of manufacturing process improvements.
Completion of all assigned work activities in adherence to the company’s Quality Management System which has been developed in compliance to ISO 13485:2003 and FDA Quality System Regulations CFR 21 Part 820.
Design, development, verification and implementation of process improvements and process aids/fixturing.
Equipment specification & procurement and coordination of installation, commissioning and validation.
Creation and update of manufacturing/inspection procedures compliant with GMP.
Root cause analysis and implementation of corrective actions as part of CAPA process.
Development of product packaging and packaging processes in conjunction with R&D.
Monitoring of process yield.
Providing ongoing input to PFMEA.
Processing of change notifications and completion of technology transfer activities in conjunction with manufacturing sub-contractor.
Participation at operations, manufacturing sub-contractor and vendor meetings.


B.Eng in Engineering/Biomedical/Manufacturing Technology (Hons degree an advantage).
Minimum 4 years relevant work experience in a Medical Device environment.
Strong understanding of medical device quality & regulatory systems.
Strong communication & organizational skills.
Ability to work in a team.
Strong analytical and problem solving skills.
Experience of fixture/process aid development.
Experience of manufacturing process development and process validations.
Working knowledge of a 3D CAD package (Solidworks an advantage).
Experience of applying Lean/Six Sigma techniques to improve manufacturing processes (Green/Black Belt certification an advantage).
Understanding of EHS and equipment safety standards.

James Cassidy | Tel: +353 (0) 1 5079250