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Job Code: 30004600   

Segment: INDUSTRIAL SOLUTIONS (50127625) 

Business Unit: MEDICAL (50126885) 

Building: Creganna Unlimited Company (CM1) 

Band/Level: 5-2-C 

Hiring Manger: Pat Gorman 

Recruiter: Fiona McLoughlin 


Travel: None 

Employee Referral Amount: $4,000.00 

Education Experience: Bachelors Degree (High School +4 years) 

Employment Experience: 3-5 years



Company Information


As one of the largest business units of TE Connectivity, TE Industrial is a leading global solutions provider with a broad portfolio of components and system solutions for clients in various industries. The growing demand for personalized products, a never-ending stream of new market requirements, the need for consistently high product quality, and an increasing interconnectedness make the use of highly advanced production systems a must. TE’s Industrial solutions provide the basis for this flexible production — by helping our customers to become more connected, addressing Smart Factory needs, connect and transmit vast amounts of data quickly, enable connectivity in harsh environments, increase productivity, meet localized manufacturing needs, and realize energy efficiency requirements. Industrial’s primary goals include enabling smarter automation, enabling smarter rail transportation, and empowering intelligent buildings.



Job Responsibilities


  • Demonstrates commitment to the Quality Policy (product safety and quality) through the daily execution of sound quality practices.
  • Leads quality related projects within the Device Manufacturing Value Stream e.g. where significant process changes are required that originates from a CAPA or a customer complaint.
  • Leads cost improvement projects and NRE activities within the value stream from a quality perspective.
  • Leads quality support for the transfer of new product into device manufacturing.
  • Provides additional support to the operations team when a new product is introduced to the value stream where required until the product has reached steady state.
  • Completion of TAP analysis for new products introduced to the value stream.
  • Leads validation activities within the value stream in conjunction with the validation group including MVP’s, MVR’s, TMV’s, OQ/PQ, PPQ and revalidation assessments.
  • Manages the approval of supplier change notifications. 
  • Supports audits for the value stream from external regulatory agencies and customers and leads preparation activities in advance of such audits.
  • Updates quality procedures, specs as required through the change plan process.
  • Provides root cause analysis & problem-solving guidance and mentoring.




  • Level 8 degree in Science, Engineering or related subject. 
  • 5-7 years’ relevant supplier quality / quality operations experience in GMP manufacturing environment in Medical Device/Pharma industry.



Key Requirements


  • Significant project management experience.
  • Very experienced in new product introductions.
  • Excellent knowledge of equipment qualifications, test method validation and process validation.
  • Ability to work as a team member and to provide mentorship to other team members.
  • Excellent communication and interpersonal skills and have demonstrated the ability to lead in a previous role.
  • Good organization and investigation skills are required.
  • A Black Belt qualification would be an advantage.
  • Excellent “hands-on” technical skills.
  • Excellent communication skills.


  • Values: Integrity, Accountability,Teamwork, Innovation

Galway, G, IE, H91

Travel:  None
Requisition ID:  45047
Alternative Locations: 

Job Segment: Quality Engineer, Manufacturing Engineer, Senior Quality Engineer, Engineer, Engineering, Quality

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