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Quality Technician - Weekend 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

Weekend Shift Hours: Friday, Saturday & Sunday - 6am - 6pm

 

The Quality Operations Technician is a member of the Operations Quality group. They will work as part of a team to maintain high quality/performance standards on all Creganna Medical products. Reporting to the Area Operations Senior Quality Engineer, 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.

 

TE Connectivity’s Quality and Reliability Engineering Teams analyze the ability of product and production systems to comply with customer and contractual requirements through established reliability factors. They design, recommend revisions and install quality control systems, develop and document analytical methods for establishing reliability of products and their components and conduct analysis on relative reliability with regards to cost, structure, weight, maintainability, facility of production, and availability of materials and equipment. Out teams develop, implement and monitor company environmental safety programs and policies to ensure compliance with federal, state, and local environmental, health and safety regulations and recommend corrective actions if necessary. They are responsible for policies and practices to comply with applicable government regulations and industry requirements related to product environmental compliance, the implementation and management of technical and testing standards and specifications, quality control and reliability programs governing materials, product and processes, resulting in the optimization of material and labor, as well as failure analysis, root cause, corrective action and customer communication.

Job Responsibilities

  • Working with the Manufacturing teams promote the achievement of the Health and safety goals.
  • Deliver on all KPIs that help the business achieve its goal.
  • Implement corrective action on issues as they arise.
  • Disposition non-conformances’, 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)
  • Review of sterilisation documentation and the release of sterilised product for shipping.
  • 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 NPI/manufacturing Operations area projects and initiatives e,g, Kaizen, yield improvement, cost reduction etc.

What your background should look like:

Qualifications

  • Level 6 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 2+ years’ industry experience in a medical device manufacturing environment.

 

Key Requirements

  • 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

About TE Connectivity
TE Connectivity is a global industrial technology leader creating a safer, sustainable, productive and connected future. Our broad range of connectivity and sensor solutions, proven in the harshest environments, enable advancements in transportation, industrial applications, medical technology, energy, data communications and the home. With approximately 80,000 employees, including more than 7,500 engineers, working alongside customers in approximately 140 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at www.te.com and on LinkedIn, Facebook, WeChat and Twitter.

 

What TE Connectivity offers:
We offer competitive total rewards compensation. Our commitment to our associates includes offering benefit programs that are comprehensive, competitive and will meet the needs of our associates.

  • Generous 401(k) Plan
  • Tuition Reimbursement
  • Benefits start on day one
  • Charity Donation Matching Program
  • Competitive Paid Time Off
  • Employee Resource Groups
  • Employee Stock Purchase Program
  • Healthcare for Associates and Families
  • Health and Wellness Incentives
  • Life Insurance and Disability Protection

Throughout our Global reach and various Business Units, we take a balanced approach to the benefits we provide. Many benefits are company-paid, while others are available through associate contribution. Specific benefit offerings can vary by location.

Location: 

GALWAY, G, IE, H91 VN2T

City:  GALWAY
State:  G
Country/Region:  IE
Travel:  None
Requisition ID:  71042
Alternative Locations: 
Function:  Quality


Job Segment: Technician, Engineer, Maintenance, Developer, Quality, Technology, Engineering, Manufacturing

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