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
Kevin Silke
Life Science

01 507 9255
[email protected]
Connect with me on
Risk Manager
Dublin
Regulatory Affairs Specialist
Republic of Ireland
Quality Engineer
Limerick
GMP Inspector
Dublin
VP of R&D
Galway
R&D Engineer
Galway
Process Engineer
Limerick
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

Process Development Engineer


Reference:KG-AAMD-126587 Location: Galway
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed

Would you like to join a leading medical device company in Galway to further develop your career? This is an excellent opportunity for an experienced Process Development Engineering professional.

You will focus on designing and developing cutting edge technologies for the manufacture of class III medical devices. You will be directly involved in the development of innovative products and processes for use in medical procedures.

Responsibilities
• As an engineer you will actively participate in all areas of product transfers including the following: Design, Technology development & advancement, Automation, Vendor management, Manufactuirng & Project management.
• You will support all activities related to equipment development and validation to meet internal and regulatory (CE) requirements.
• You will support process development, characterization and validation activities.
• You will use Design, Reliability & Manufacturability methodology (DRM), 3-D drawing/printing and Augmented reality to develop best in class technologies for the manufacture of our medical device product ranges.
• You will collaborate with cross functional teams to define, execute and deliver on program deliverables.
• You will utilize your new and existing skillsets in six sigma tools, project management and technology development to solve technical problems.
• You will compile, document and present all learnings to project and functional teams.

KEY SKILLS & EXPERIENCE
• Third Level 8 Degree or higher in Electronic, Electrical, Mechanical or Biomedical Engineering or related discipline and desirably with experience in a similar role.
• Dynamic team player and can work effectively and proactively on cross-functional teams
• Knowledge of medical device processes with a good understanding of product and process design.
• Develops technical / Equipment documentation including Equipment binders , Equipment validations and technical reports in accordance with quality system requirements.
• Support the development and sourcing of vendors, Co-ordinate and liaise with vendors to ensure equipment is sourced to budget and on time.
• Supports verification, validation, and implementation of equipment for both design and process development.
• Utilizes knowledge of FDA and ISO / CE / EH&S requirements related to equipment / process development, ensuring robust validation and qualification.

If you meet the Key Skills and Experience, and feel you are a good fit for this role, please apply today!