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
Sean McCarthy
Life Science

+3530212339371
[email protected]
Connect with me on
QC Analyst
Dublin
R&D Engineer
Limerick City
Production Team Lead
Dublin South
PLC Programmer
Limerick
Project Manager
Limerick
EHS&S Manager
Waterford
Senior R&D Engineer
Limerick City
C&Q Engineer
Dublin
Quality Engineer
Limerick
PLC Programmer
Limerick
Process Lead
Donegal
Quality Engineer
Limerick
R&D Manager
Limerick
EHS Trainer
Dublin
Regulatory Affairs Specialist
Republic of Ireland
Project Engineer
Limerick
NPI Manager
Dublin
Project Engineer
Limerick
Controls Engineer
Dublin South
GMP Inspector
Dublin
Project Engineer
Limerick
Process Engineer
Limerick
Process Engineer
Republic of Ireland
Head of R&D
Galway
Project Engineer
Limerick
QA Contractor
Dublin City Centre
Quality Specialist
Tipperary
R&D Manager
Galway
GCP Inspector
Dublin
R&D Engineer
Galway
NPD Manager
Galway
Senior CSV Specialist- Hybrid
Republic of Ireland
QA Manager
Dublin
R&D Engineer
Dublin
Engineering Technician
Dublin South
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

Senior Project Engineer


Reference:SMC6475 Location: Cork
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Project Engineer

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


• Lead NPI development requirements and work with cross functional teams in the Innovation Centre and with the Value Streams.
• Provide design for manufacturing technical input to global design groups to minimise lifecycle cost
• Project planning to deliver project(s) against agreed milestones and project scope (schedule, resource, cost).
• Deliver stable manufacturing solutions in line with stability metrics process.
• Conduct and lead detailed product design reviews
• Development of advanced manufacturing processes to lean guidelines
• Manage risk management and validation lifecycle for new process or process changes.
• Management of the Asset Lifecycle for new equipment and processes (URS/RA/IQ/OQ/PQ).
• Direct PFMEA studies and lead risk assessment effort for overall process
• Influence innovative qualification methodologies to apply appropriate statistical and validation techniques based on failure model and overall risk
• Develop strategic collaborations across functions, business units and geographic boundaries to achieve effective outcomes over the long-term.
• Provide timely and accurate reporting on project activities.
• All other duties as directed by direct manager.



Education & Experience

• Obtained as a minimum a Degree in Mechanical/Production/Manufacturing Engineering and 3 years minimum post graduate (Ideally 5 years plus) experience in a medical device or comparable hi-tech environment.
• Proven track record in development, installation and qualification of manufacturing processes for New Products or Product Transfer.
• Experience using proven problem solving/Root techniques (8D, TRIZ or equivalent)
• Certification from an accredited institution in Project/Program Management.
• Knowledge of medical device quality & regulatory systems and medical device directive (ISO13485, MDD and FDA CFR 820) and other pertinent Design Control requirements.