TE Connectivity Quality Technican- Night Shift in Galway, Ireland
TE Connectivity (NYSE: TEL) is a $12 billion global technology leader. Our connectivity and sensor solutions are essential in today’s increasingly connected world. 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.
The Operations Quality Technician is a member of the Operations Quality group.
S/he will work as part of a team to maintain high quality / performance standards on all Creganna products.
Reporting to the area Operations Snr Quality Engineer or Manager, the position will be challenging and will require an ability to participate in a cross functional team and work on own initiative and with minimum supervision
Key Job Responsibilities:
Support relevant prototype/manufacturing areas to achieve targets.
Implement corrective action on issues as they arise.
Disposition NCR’s, conduct & determine root cause analysis including corrective actions.
Conduct area GMP/GDP 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.
Conduct process audits against Quality System requirements.
Support all QA related documentation activities (i.e. Raise ECO’s, 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.
Have a basic knowledge of ISO/FDA/MDD and other Product Development related regulatory requirements
Have an understanding of standard metrology good practice.
Provide support for internal and external audits to ISO and FDA requirements.
Support prototype/manufacturing Operations area projects and initiatives i.e. Kaizen, CFPS etc.
Other tasks as directed by the functional area Quality Engineer in line with company goals and objectives.
Certificate/Diploma in Science / Engineering / Quality Management or related fields essential.
Minimum of 1yrs industry experience in a medical device-manufacturing environment.
Clear understanding 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.
New product introduction and manufacturing process transfer experience 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.
Requisition ID: 2017-82966
Business Unit (Current): Industrial Solutions - Medical - Creganna Medical
External Company URL: www.tycoelectronics.com