191 Senior Manufacturing Engineer jobs in Ireland

Manufacturing Engineer
**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**
The Manufacturing Engineer in a sustaining role focuses on maintaining and improving existing manufacturing processes to ensure consistent production of high-quality medical devices. This role is integral to troubleshooting issues, implementing process improvements, and supporting ongoing production activities while maintaining compliance with regulatory and quality standards.
This includes advanced automated manufacturing processes such as laser processing (ablation/welding) and moulding.
**Job Requirements**
+ **Process Support & Troubleshooting:**
+ Provide day-to-day technical support to resolve production challenges, minimize downtime, and ensure stable operations.
+ Analyse root causes of production issues and implement corrective actions to address defects or inefficiencies. **Continuous Improvement:**
+ Identify and implement opportunities to improve yields, reduce waste, and enhance overall production efficiency.
+ Utilize Lean Manufacturing, Six Sigma, and other methodologies to drive process enhancements. **Change Management:**
+ Lead or support engineering changes (ECOs) to existing products, processes, or equipment.
+ Validate and document changes to ensure they meet quality, compliance, and operational requirements. **Equipment & Tooling Maintenance:**
+ Ensure the continued functionality of production equipment through preventative maintenance programs.
+ Support equipment upgrades or replacements to improve reliability and performance **.** **Collaboration with Cross-functional Teams:**
+ Partner with Quality, Operations,NPDand Supply Chain teams to address process deviations, non-conformances, and supplier issues. **Documentation & Reporting:**
+ Maintain accurate process documentation, including SOPs, work instructions, validation protocols, and technical reports.
+ Track and report key performance metrics, such as yields, downtime, and defect rates. **Health & Safety**
+ Ensure that all Health, Safety and Environmental requirements are fulfilled.
**What your background should look like**
**Qualifications**
+ Engineering level 8 degree, or equivalent qualification.
+ Preferably a minimum of 3 years' experience in a similar roles
**Key Requirements**
+ Strong problem-solving and troubleshooting skills.
+ Ability to prioritize tasks and manage multiple ongoing projects.
+ Excellent communication and collaboration skills to work with cross-functional teams.
+ Experience with automated production lines, moulding, and laser welding (definite advantage).
+ Must be able to plan, organize, and implement multiple concurrent tasks and projects.
+ Jigs & Fixtures design and maintenance experience would be an advantage.
+ Demonstrate a practical understanding of lean manufacturing principles and statistics.
+ Equipment and Process Validation experience with working knowledge of Minitab software.
+ SolidWorks /AutoCAD skills would be an advantage.
+ Knowledge of ISO & FDA compliance.
+ Demonstrate a dynamic, motivated & flexible approach to work with results-oriented attitude.
**Competencies**
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork
**ABOUT TE CONNECTIVITY**
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( TE CONNECTIVITY OFFERS:**
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!
- Competitive Salary Package
- Performance-Based Bonus Plans
- Health and Wellness Incentives
- Employee Stock Purchase Program
- Community Outreach Programs / Charity Events
- Employee Resource Group
**IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD**
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from** **actual** **email addresses ending in @te.com** . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.
Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site.
Location:
GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: None
Requisition ID:
Alternative Locations:
Function: Engineering & Technology
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.

Manufacturing Engineer
**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**
Working within the core Engineering group, and reporting to the Senior Engineer, the Manufacturing Engineer - must be motivated in delivering improvements and making a positive difference to be successful in such a role, sharing a desire for excellence, a value for the company you are working for. You will have the ability to analyse data and complete root cause analysis as essential skills gained within the manufacturing environment. The Engineer will support Technicians in a Manufacturing environment and be responsible for supporting all engineering activity in areas of responsibility.
**Job Requirements**
+ Work with key business stakeholders and operations teams to build a continuous improvement environment that supports ongoing change and improvement initiatives.
+ Support the delivery of better value and greater efficiency through the identification and elimination of unnecessary complexity within Balloon forming processes and identification of simplified ways of working.
+ Identify and put in place permanent and effective technical / system solutions to quality and technical problems.
+ Implement equipment maintenance procedures for critical equipment.
+ Investigate new process technologies and evaluate potential competitive advantage and the cost-benefit of introduction.
+ Consistently meet customer requirements and commitment to excellence in performance and meeting deadlines.
+ Maintain high quality/compliance standards in line with Medical Devices manufacturing requirements within Creganna Medical, part of TE Connectivity.
+ Resolving quality and technical issues such that impact on product supply to customers is minimized.
+ Maintain high quality / compliance standards in line with Medical Devices manufacturing requirements within Creganna Medical, part of TE Connectivity.
+ Work as part of Production Support team to drive product and process improvements/developments.
+ Update Manufacturing procedures, specs as required through change control process.
+ Ensure that all Health, Safety and Environmental requirements are fulfilled.
+ Projects - identify and implement continuous improvement projects to reduce scrap across the business unit.
+ New equipment introductions - EIQ/EOQ, DOE & Process OQ/PQ Validations.
**What your background should look like**
**Qualifications**
+ Level 8 Polymer degree, or equivalent.
+ Preferably a minimum of 1 years' experience in a similar role.
**Key Requirements**
+ Experience in Med Device distinct advantage.
+ Demonstrated experience in Process troubleshooting
+ Designed and validated new manufacturing methods and equipment in collaboration with vendors
+ Must be able to plan, organize, and implement multiple concurrent tasks and projects.
+ Jigs & Fixtures design and maintenance experience would be an advantage.
+ Demonstrate a practical understanding of Lean Manufacturing principles and statistics.
+ Demonstrate operating knowledge of Minitab software, would be an advantage.
+ SolidWorks /AutoCAD skill would be an advantage.
+ Demonstrate a dynamic, motivated & flexible approach to work with results-oriented attitude.
+ Excellent communication, planning and organisational skills.
+ Knowledge of ISO & FDA compliance.
**#jobsEMEANR**
**#LI-ONSITE**
**Competencies**
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork
**ABOUT TE CONNECTIVITY**
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( TE CONNECTIVITY OFFERS:**
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!
- Competitive Salary Package
- Performance-Based Bonus Plans
- Health and Wellness Incentives
- Employee Stock Purchase Program
- Community Outreach Programs / Charity Events
- Employee Resource Group
**IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD**
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from** **actual** **email addresses ending in @te.com** . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.
Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site.
Location:
GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: 10% to 25%
Requisition ID:
Alternative Locations:
Function: Engineering & Technology
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.

Purpose of Role:
The Manufacturing Engineer (ME) will provide engineering and process support to ensure successful implementation of 2D barcoding in line with EU MDR requirements.
This role will focus on supporting technical strategy execution, process validation, and operational readiness across both internal manufacturing and supplier sites.
Key Responsibilities:
+ Support technical execution of 2D barcode implementation, including validation activities (VP, IQ, OQ, PQ).
+ Partner with Quality Engineers (QEs) and Supplier Quality Engineers (SQEs) to assess and confirm laser marking equipment compatibility and process qualification at both supplier and internal sites.
+ Assist in First Article Inspection (FAI) preparation, reviewing supplier provided verification data and ensuring compliance to marking requirements.
+ Update and maintain manufacturing documentation (DCP, PFMEA, SOPs) to reflect new barcoding processes.
+ Collaborate with operations teams to ensure inspection readiness (visual inspection, barcode verifier checks).
+ Troubleshoot and provide technical support during initial marking trials and confidence runs.
+ Support scrap management, label obsolescence, and carton switchovers as required for Go-Live phases.
+ Actively contribute to risk assessments, ensuring process robustness and alignment with MDR and GMP requirements.
Required Skills & Experience:
+ 2-4 years' experience in a regulated manufacturing environment (medical device preferred).
+ Exposure to process validation and FAI/PPAP activities in a regulated environment.
+ Familiarity with laser marking or UDI/2D barcoding processes desirable.
+ Strong problem solving and root cause analysis capability (Six Sigma / Lean tools beneficial).
+ Proven ability to work collaboratively with cross functional teams (QE, SQE, and Operations).
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

Manufacturing Engineer About Your New Employer Join a leading medical device company in Galwayknown for its innovative solutions and commitment to improving patient care. With a strong presence in the market and a reputation for excellence, this company offers exciting projects and a dynamic work environment. The company values its employees and provides opportunities for growth, development, and career advancement. About Your New Job As a Manufacturing Engineer, you will be responsible for developing, implementing, and improving manufacturing processes to ensure the production of high-quality medical devices. You will work closely with cross-functional teams, including R&D, Quality, and Operations, to support new product introductions and continuous improvement initiatives. You will analyze and troubleshoot manufacturing issues, identify root causes, and implement corrective actions to enhance productivity and efficiency. You will develop and maintain documentation, including process flow diagrams, work instructions, and validation protocols, ensuring compliance with regulatory requirements. You will support the implementation of lean manufacturing principles and drive process optimization projects to reduce costs and improve overall operational performance. What Skills You Need Bachelors Degree in Engineering, preferably in Mechanical, Biomedical, or Manufacturing Engineering. Minimum 3-5 years of experience in a manufacturing engineering role within the medical device industry. Strong understanding of manufacturing processes, including assembly, machining, and automation. Experience with process validation, equipment qualification, and regulatory compliance (e.g., FDA, ISO 13485). Proficiency in CAD software (e.g., SolidWorks, AutoCAD) and familiarity with statistical analysis tools (e.g., Minitab). Excellent problem-solving skills and ability to work in a fast-paced, team-oriented environment. Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams. Self-motivated individual with a deadline-oriented focus and a commitment to continuous improvement. Whats on Offer Competitive salary Benefits, Training & Development, Career Path Opportunity to work in a dynamic and collaborative environment Chance to contribute to the development of life-saving medical devices and make a real impact on patient care Whats Next Apply now by clicking the Apply Now" button or contact . Or if the job isnt quite right but you are looking for something similar, please get in touch. We also have multiple Temp, FTC and Contract jobs available. Skills: manufacturing SOPs Kaizen lean manufacturing

Manufacturing Engineer Dundalk €40k - €45k Vickerstock is currently working in partnership with one of the Irelands most succesful manufacturing firms to assist them with the recruitment of a Manufacturing Engineer. You will work with some of the most talented individuals in the industry to assist with the lean manufacturing practises across the site. Your key responsibilities as a Manufacturing Engineer Lead the day-to-day delivery of the CI process through the site functions. Be an integral member of a team of multi-skilled stream experts to deliver and exceed targeted KPI's, focussed on a comprehensive fault finding and analysis process. Support team with root cause identification and solutions designed to prevent repeated failures using lean tools and techniques. Liaise with department streams through Kaizens, understanding issues and setting plans to resolve. Carry out technical reviews with PSM & Engineering Lead on core systems and work with suppliers to optimise across site Update / maintain all asset documentation as required such as machine settings, manuals, PLC back-ups, labelling & PPM schedules resulting from CI works. Document and train maintenance Standard Work and Standard Operating Procedures arising from CI works. Apply analytical data techniques to prioritise work in conjunction with the Production Streams. As a Manufacturing Engineer, ideally you will have. An industry recognised qualification in Mechanical or Electrical Engineering At least 2 years' experience in manufacturing environment Proven problem solving skills. What we hope you will do next; Contact Warren Watson to discuss this in absolute confidence or send an updated CV via the link on the page. By applying for this role, you accept the terms of processing, please find our privacy policy on our website. As an experienced specialist senior engineering and manufacturing recruitment professional with 7 years' experience; I personally specialise within the recruitment of Lean Engineers at all levels across Ireland. If you are interested in this vacancy, or work within Lean Engineering / Manufacturing in Ireland, then please apply with your CV to me for consideration - (You can also find and connect with me on LinkedIn) Skills: Manufacturing Engineer Process Engineer Lean.

Job Title: Manufacturing Change Engineer Salary: Competitive Job Type:Permanent Location:Co. Louth Ref: S RecruitmentPlus on behalf of our client are seeking a Manufacturing Change Engineerto join a successful engineering company who will manage the process of altering existing manufacturing systems to improve efficiency, product quality and safety. This will be an interesting and varied role and will involve designing and implementing new processes, equipment and technologies. Requirements: Qualified to degree level BS/MS in Mechanical Engineering or a related technical field with 1+ years experience in engineering change in a manufacturing environment. Lean Six Sigma Green Belt or equivalent. Knowledge and understanding of Mechanical, Electrics/Electronics, Assembly work, Hydraulics, Assembly Instructions and Safe working practices. Ability to work on own initiative, to come up with solutions and problem solve Ability to Review Mechanical and Technical Drawings to support engineering. Agility and personal adaptability with the ability to successfully manage multiple priorities with a high sense of urgency in a rapidly changing environment. Experience in using ERP systems. Some Experience with CAD would be beneficial. Key Duties & Responsibilities: Continuously improve the application of 6S, Kaizen, going to Gemba to increase safety and performance. Responsible for the implementation of Engineering Change Orders or New Product Development into the manufacturing environment, including new part configuration and set-up, management of open production orders, manufacturing routing and master data management and assembly instruction updates. Develop Standard Operating Procedures within the A.Is that encompass safe working practices. Promote Leader Standard Work systems of audit and daily management to sustain improvements in safety. Process improvement skills including the use of Lean tools to drive increased manufacturing Quality performance. Develop daily improvement processes through Lean Daily Management Structures. Move the company towards digital instructions and move away from paper based processes. Working with the Design Engineering Process change owner to ensure the best effectivity dates are achieved to limit obsolete stock. Working with the sourcing team to update and maintain the use of PFEP (Plan For Every Part) to establish inventory amounts, locations and replenishments Establish processes that utilise the use of JIT (Just In Time) reducing work in progress. Analysis, modelling and simulation of production based big data from sensors and devices to support development on our Manufacturing Excellence Systems (MES). Use of digital devices (e.g. tablets, smartphones, smartwatches) for production monitoring and control. Continuously work with the site leadership and value stream managers to analyse data to establish opportunities for improvement. Review delivery performance with the Value Stream Managers and Site Leadership to identify and deliver improvement using continuous improvement tools. Uses the kaizen events to continually improve delivery performance with tangible results. Acting on engineering change orders in a timely fashion ensuring the changes are implemented with zero impact to production. Monitor data integrity within our ERP system, actively looking for errors and amending any setup errors. Promotes a Continuous Learning environment through development and delivery of all intellectual property. Promote a culture of employee engagement with the use of Kaizen to engage teams. Bring to life each day our values and demonstrate these behaviours. If you have the relevant qualifications and experience and are interested in this position, please apply now and Ciara who is based in our Northeast office will be in contact if you are suitable. If you are living in Ireland and hold a VALID WORK PERMIT, please feel free to contact us directly. However, if you do not hold a valid work permit unfortunately we will not be in a position to assist you with your job search. Recruitment Plus is not in a position to respond to each individual application due to the high volume of submissions. We will only contact those candidates whose CV matches the criteria for the vacancy. Thank you for your patience. For detailson our privacy policy please click here: Skills: Manufacturing Engineer Mechanical Engineer Six Sigma Lean Manufacturing Change Order Change Engineering Green Belt

Manufacturing Engineer About Your New Employer Join a leading medical device company in Galwayknown for its innovative solutions and commitment to improving patient care.

With a strong presence in the market and a reputation for excellence, this company offers exciting projects and a dynamic work environment.

The company values its employees and provides opportunities for growth, development, and career advancement.

About Your New Job As a Manufacturing Engineer, you will be responsible for developing, implementing, and improving manufacturing processes to ensure the production of high-quality medical devices.

You will work closely with cross-functional teams, including R&D, Quality, and Operations, to support new product introductions and continuous improvement initiatives.

You will analyze and troubleshoot manufacturing issues, identify root causes, and implement corrective actions to enhance productivity and efficiency.

You will develop and maintain documentation, including process flow diagrams, work instructions, and validation protocols, ensuring compliance with regulatory requirements.

You will support the implementation of lean manufacturing principles and drive process optimization projects to reduce costs and improve overall operational performance.

What Skills You Need Bachelors Degree in Engineering, preferably in Mechanical, Biomedical, or Manufacturing Engineering.

Minimum 3-5 years of experience in a manufacturing engineering role within the medical device industry.

Strong understanding of manufacturing processes, including assembly, machining, and automation.

Experience with process validation, equipment qualification, and regulatory compliance (e.g., FDA, ISO 13485).

Proficiency in CAD software (e.g., Solid Works, Auto CAD) and familiarity with statistical analysis tools (e.g., Minitab).

Excellent problem-solving skills and ability to work in a fast-paced, team-oriented environment.

Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.

Self-motivated individual with a deadline-oriented focus and a commitment to continuous improvement.

Whats on Offer Competitive salary Benefits, Training & Development, Career Path Opportunity to work in a dynamic and collaborative environment Chance to contribute to the development of life-saving medical devices and make a real impact on patient care Whats Next Apply now by clicking the Apply Now" button or contact.

Or if the job isnt quite right but you are looking for something similar, please get in touch.

We also have multiple Temp, FTC and Contract jobs available.

Skills: manufacturing SOPs Kaizen lean manufacturing

Are you a Quality/Manufacturing engineer looking for a new opportunity? Don't hesitate and apply today! PROJECT DESCRIPTION We are seeking experienced Remediation Quality Engineers / Manufacturing Engineers to support a site-wide remediation program following an FDA 483. These roles will focus on manufacturing process validation, quality system updates, and documentation remediation. Consultants will be based onsite and work directly with manufacturing and quality process owners to identify compliance gaps, implement corrective actions, and ensure documentation is accurate and audit-ready. The project will involve tackling remediation areas in sequence, updating technical files and procedures, and ensuring robust validation of manufacturing processes. Consultants must be able to take a problem statement through to a compliant solution, collaborating cross-functionally across Quality, Manufacturing, and Regulatory teams. PROJECT DESCRIPTIONPartner with process owners on the floor to capture and remediate issues.Support process validation (IQ/OQ/PQ) and documentation updates.Drive CAPA/NCR closure and implement compliant solutions.Provide technical writing for quality and manufacturing documents.Collaborate cross-functionally to ensure regulatory compliance. CONSULTANT RESPONSIBILITIESEngineering or Quality degree with 5-10 years' med-tech experience.Background in remediation, process validation, CAPA, NCRs.Strong technical writing and documentation skills.Knowledge of 21 CFR Part 820, ISO 13485.LOCATION: Cork

Manufacturing Engineer (Balloons)
**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**
Working within the core Engineering group, and reporting to the Senior Engineer, the Manufacturing Balloons Engineer - must be motivated in delivering improvements and making a positive difference to be successful in such a role, sharing a desire for excellence, a value for the company you are working for. You will have the ability to analyse data and complete root cause analysis as essential skills gained within the manufacturing environment. The Engineer will support Technicians in a polymer Balloons environment and be responsible for supporting all engineering activity in areas of responsibility.
**Job Requirements**
+ Work with key business stakeholders and operations teams to build a continuous improvement environment that supports ongoing change and improvement initiatives.
+ Support the delivery of better value and greater efficiency through the identification and elimination of unnecessary complexity within Balloon forming processes and identification of simplified ways of working.
+ Identify and put in place permanent and effective technical / system solutions to quality and technical problems.
+ Improve Balloon forming manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing methods and equipment; conferring with equipment vendors.
+ Implement equipment maintenance procedures for critical equipment.
+ Investigate new process technologies and evaluate potential competitive advantage and the cost-benefit of introduction.
+ Consistently meet customer requirements and commitment to excellence in performance and meeting deadlines.
+ Maintain high quality/compliance standards in line with Medical Devices manufacturing requirements within Creganna Medical, part of TE Connectivity.
+ Resolving quality and technical issues such that impact on product supply to customers is minimized.
+ Maintain high quality / compliance standards in line with Medical Devices manufacturing requirements within Creganna Medical, part of TE Connectivity.
+ Work as part of Production Support team to drive product and process improvements/developments.
+ Update Manufacturing procedures, specs as required through change control process.
+ Ensure that all Health, Safety and Environmental requirements are fulfilled.
+ Projects - identify and implement continuous improvement projects to reduce scrap across the business unit.
+ New equipment introductions - EIQ/EOQ, DOE & Process OQ/PQ Validations.
**What your background should look like**
**Qualifications**
+ Level 8 Polymer degree, or equivalent.
+ Preferably a minimum of 4 years' experience in a similar role.
**Key Requirements**
+ Experience on Balloon forming processes a distinct advantage.
+ Demonstrated experience in Process troubleshooting
+ Designed and validated new manufacturing methods and equipment in collaboration with vendors
+ Must be able to plan, organize, and implement multiple concurrent tasks and projects.
+ Jigs & Fixtures design and maintenance experience would be an advantage.
+ Demonstrate a practical understanding of Lean Manufacturing principles and statistics.
+ Demonstrate operating knowledge of Minitab software, would be an advantage.
+ SolidWorks /AutoCAD skill would be an advantage.
+ Demonstrate a dynamic, motivated & flexible approach to work with results-oriented attitude.
+ Excellent communication, planning and organisational skills.
+ Knowledge of ISO & FDA compliance
**#jobsEMEANR**
**#LI-ONSITE**
**Competencies**
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork
**ABOUT TE CONNECTIVITY**
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( TE CONNECTIVITY OFFERS:**
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!
- Competitive Salary Package
- Performance-Based Bonus Plans
- Health and Wellness Incentives
- Employee Stock Purchase Program
- Community Outreach Programs / Charity Events
- Employee Resource Group
**IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD**
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from** **actual** **email addresses ending in @te.com** . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.
Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site.
Location:
GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: 10% to 25%
Requisition ID:
Alternative Locations:
Function: Engineering & Technology
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.