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Quality & Reliability Technician - Night Shift

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. 

Job Overview

TE Connectivity (NYSE: TEL) is a $12 billion global technology leader. We collaborate with engineers to transform their concepts into creations – redefining what’s possible using intelligent, efficient and high-performing TE products and solutions proven in harsh environments. Our 72,000 people, including over 7,000 engineers, partner with customers in over 150 countries across a wide range of industries. We believe EVERY CONNECTION COUNTS – www.TE.com.   

Creganna Medical is ranked among the top 10 global companies in the medical device outsourcing industry. In recent years the company has developed from a component manufacturer to also offer specialization in the design and manufacture of minimally invasive delivery and access devices for a range of therapies. Serving over 400 companies across 30 countries, Creganna Medical’s customers include the world’s leading medical device and life science companies. Headquartered in Galway, Ireland, Creganna Medical has a global operational footprint with design and manufacturing facilities spanning the U.S., South America, Europe and Asia.  http://www.creganna.com/
 

Job Responsibilities

•Support relevant manufacturing areas to achieve targets.
•Implement corrective action on issues as they arise.
•Disposition nonconformances’, conduct & determine root cause analysis including corrective actions.
•Conduct area practice v’s procedure/Good Documentation Practice audits and follow up on findings to ensure satisfactory closure.
•Follow up on Corrective Actions for in-process and customer complaint issues.
•In-process sampling and testing and subsequent report writing.
•Conduct First Article Inspections on product as required.
•Processing procedure changes.
•Support all QA related documentation activities (i.e. Raise Change plans, write procedures etc)
•Support functional area validation activities.
•Support Fault Analysis and Scrap Reduction activities.
•Participate/drive quality improvement projects/activities.
•Participate in preparing & on-going maintenance of FMEAs and Control Plans. Reporting function Quality metrics.
•Support manufacturing Operations area projects and initiatives e,g, Kaizen, yield improvement, cost reduction etc.
•Other tasks as directed by the functional area Quality Engineer in line with company goals and objectives. 
•Provide support for internal, customer and external audits to ISO and FDA requirements.
 

What your background should look like:

•Level 6/7 degree in Science / Engineering / Quality Management or related fields essential is a minimum requirement. A level 8 degree in one of these areas would be a distinct advantage.
•Minimum of 1 years’ industry experience in a medical device manufacturing environment.
•A problem-solving qualification (either Green or Yellow belt) preferred. 
•Clear understanding of medical device quality systems and requirements.
•Experience in product inspection techniques.
•Knowledge of root cause analytical and problem-solving skills.
•Knowledge of FDA and ISO Quality systems for Medical device companies desirable.
•Demonstrated excellent organizational skills and ability to work on own initiative essential.
•Excellent written and verbal communication skills essential.
•Computer literate, MS Word, Excel, PowerPoint.

Competencies

Values: Integrity, Accountability,Teamwork, Innovation
Location: 

GALWAY, G, IE, H91 VN2T

City:  GALWAY
State:  G
Country/Region:  IE
Travel:  None
Requisition ID:  79421
Alternative Locations: 
Function:  Engineering & Technology


Job Segment: Technician, Maintenance, Engineer, Night, Technology, Quality, Manufacturing, Engineering, Operations

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