197 Manufacturing 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.

**Who we are:**
Abbott has a presence in over 160 countries and has over 113,000 employees. Our new manufacturing facility in Kilkenny (R95 A02A) is Abbott's 7th manufacturing site in Ireland.
The facility is a centre for world-class engineering, quality, medical device manufacturing. We have been making a difference in the lives of Irish people since 1946.
**Abbott Ireland**
In Ireland, Abbott employs around 6,000 people across ten sites. We currently have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford, Kilkenny and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**What is this position:**
As Manufacturing Technician you will provide technical support relating to equipment utilized in the manufacturing areas by repairing, maintaining, or modifying production equipment.
Monitoring machine output on the shift to and ensure all cells are running to cycle time, to meet specific targets.
**What You'll Be Doing:**
+ Install and equipment validation
+ Conducting scheduled maintenance, diagnosing, and troubleshooting faults
+ Perform skilled maintenance and repair such as mechanical, pneumatics, electrical systems
+ Lead on maintenance and/or process issues
+ Ability to interpret blueprints and schematics.
+ Certifies and train manufacturing associates in the production processes.
+ Identifies and implements corrective actions for manufacturing related issues.
**How does this role fit into the organisation:**
You will report to a process Engineering Manager on a team of approx. 20. Your team will include process engineers and manufacturing technicians.
**What we're looking for:**
+ Min level 6 qualification (Trade or Third level equivalent)
+ Electrical and mechanical skills are desired
+ Technical and fault-finding skills
**What's in it for you:**
+ Pension
+ Healthcare
+ Bonus
+ Life insurance
+ Disability insurance
+ Paid maternity leave
+ Parental leave
+ Adoptive leave
+ Flexible working
Connect with us at or , on LinkedIn at , on Facebook at and on Twitter @AbbottNews.
Abbott is an equal opportunities employer
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

**About Abbott**
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in **diagnostics** , **medical devices** , **nutritionals** , and **branded generic medicines** . Our **115,000 colleagues** serve people in more than **160 countries** .
In **Ireland** , Abbott has been operating since **1946** , employing over **6,000 people** across **ten sites** , including:
+ **Six manufacturing facilities** in Clonmel, Cootehill, Donegal, Longford, and Sligo
+ A **third-party manufacturing management operation** in Sligo
+ **Commercial, support operations, and shared services** in Dublin and Galway
**Abbott Ireland Diagnostic Division - Longford**
The Longford facility plays a vital role in meeting the growing global demand for diagnostic testing in areas such as **infectious disease** , **cancer** , **thyroid** , and **cardiovascular diseases** .
Located in the heart of Ireland's midlands, Longford is surrounded by natural beauty including the River Shannon, Lough Ree, and the Royal Canal. The county offers a vibrant mix of communities, rich history, and a wide range of amenities, festivals, cultural events, and recreational activities.
**Primary Function**
The Manufacturing Manager is responsible for ensuring that the Longford facility meets its customer, regulatory, financial, and safety goals through the effective management of manufacturing and testing operations. This role supports new product and process transfers and leads strategic change initiatives to drive continuous improvement across the site.
**Key Responsibilities**
+ Lead and manage assigned manufacturing and support functions within Operations
+ Ensure major projects are delivered on time and within budget
+ Maintain product availability and meet customer requirements for diagnostic reagents
+ Drive timely completion of non-conformance investigations and CAPA activities
+ Promote a culture of continuous improvement in safety, quality, and performance
+ Optimize human resources through effective communication, teamwork, and engagement
+ Ensure compliance with GMP, HR, safety, financial, and quality procedures
+ Stay current with technical and manufacturing developments to maintain regulatory compliance
+ Manage collaboration between Longford Operations and other Abbott sites
+ Ensure quality standards are met for internal and external audits and customer expectations
+ Support strategic planning and execution of operational changes
+ Maintain operational task lists and project plans (e.g., ETMS TO DO LIST)
+ Conduct business in compliance with EHS laws and Abbott global standards
**Supervisory / Management Responsibility**
+ Direct supervision and leadership of manufacturing teams
+ Responsible for team performance, development, and motivation
**Education & Experience**
+ A relevant third-level qualification (e.g., Engineering, Science, or related discipline)
+ Minimum **5 years' experience** in a regulated manufacturing environment (Medical Device or Diagnostics preferred)
+ Minimum **3 years' experience** in people management and team motivation
+ Strong communication and problem-solving skills
+ Familiarity with regulatory requirements and quality systems
**Accountability**
+ Accountable for the performance and compliance of assigned operations
+ Decision-making within agreed product availability and performance goals
+ Operates with general guidance from senior management
+ Annual goals and performance reviews conducted with the Site Director
Connect with us at or , on LinkedIn at , on Facebook at and on Twitter @AbbottNews ( .
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

Manufacturing Specialist (Central Services) Westport, Ireland Full-time Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on , , , , and . Job Description AbbVie helps people around the world live better days and better lives each year. And that takes all of us. We are now recruiting for a Manufacturing Specialistto join our newly formed Central Cervices Team in AbbVie Westport, Co Mayo. Established in 1977, AbbVie Westport is a Centre of Excellence for Aseptic for Commercial manufacturing of Biologics & Eyecare (pharmaceutical) products. In this role you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build an inclusive culture of high performance as part of the team. Your main focus will be working on process improvement projects with cross-functional teams. This is a great opportunity to make a large impact of the future success of manufacturing eyecare products to our patients, working with a multitude of pharmaceutical manufacturing technologies, such as mold blowing, single dose, multidose and steroid manufacturing. If you are looking for a career with impact, then come and join us in our mission to provide the highest quality products and outstanding service to our patients! Is this a team you want to be part of? Then read on Key responsibilities: Support the production schedule according to customer demands from a technical perspective where and when required. Participate in performance management across the department and ensure consistency in approach from a technical perspective and aid in communication between different stakeholders. Track and measure departmental KPIs and translate them into Perfect Index relevant KPIs. Lead and promote a culture of Safety, Quality, Excellence, Continuous Improvement and drive lean initiatives by regular production GEMBAs Technical knowledge in the manufactured products and production equipment used. Support lean manufacturing on site by writing/ updating and approving SOPs Lead production related product quality investigations in conjunction with Quality Assurance and other cross-functional stakeholders including the assignment and management of corrective and preventive actions. Apply investigational tools like fishbone, 5W, contradiction matrix for root cause analysis. Ensure compliance with applicable regulatory agencies by supporting where required, also use knowledge to drive continuity and improvement on an ongoing basis Support change management and lead production aspect of CPs as part of a cross-functional team including identification and implementation of relevant tasks in a timely manner. Conduct business in compliance with all applicable laws and regulations, company policies and with highest ethical standards. Support operations in maintaining a high 5S standard Ensure you are fully informed of Shift and Dept performance metrics and have a clear understanding on how they impact overall Site Perfect Index Qualifications So, what do you need to do this role? Technical Skills and Experience: BSc in Engineering, Science, a relevant discipline, or equivalent experience required, MSc in Engineering, Science, or a relevant discipline preferred 2+ years in a GMP manufacturing environment (equivalent experience considered), aseptic manufacturing experience preferred Excellent documentation and communication skills Excellent analytical and presentation skills with the ability to work independently Ability to work towards strict deadlines Ability to build relationships with peers, influence without authority Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community? Equal Opportunity Employer/Veterans/Disabled.

Catalyx are seeking a Manufacturing Technician to join our team and work a 24/7 (4 cycle) shift on our customer site in Cork. As a Manufacturing Technician, you will require a working knowledge of manufacturing methods and procedures in our customer's pharmaceutical tableting production facility. Who We Are : Catalyx specializes in the science of operational processes. With a footprint across North America and Europe, the company carefully automates and services R&D, production, packaging, and delivery processes-globally-with a sophisticated blend of products, technologies, and lifecycle services. Catalyx is a trusted partner in delivering world-class lifecycle services to regulated and high-risk end markets. With a relentless commitment to innovation and excellence, we partner with life science and other highly regulated organisations, to empower them to enhance efficiency, and drive success. As part of this commitment, we are continuously developing our on-site teams to support the advancement of customer operations. Responsibilities: Work on routine assignments following established SOPS, Master Batch Record and cGMPs Perform moderately complex tasks associated with aseptic processing, dispensing, compaction, granulation, milling and coating Reporting any issue that needs to be resolved on line performance to Operations Lead Perform more complex troubleshooting unassisted Work on more complex manufacturing processes and assignments Clean (manually, and clean in place) and assembles equipment for production Perform detailed SAP (computerised software) and MES transactions in resolving inventory discrepancies Clean manufacturing area, including walls, ceilings, and floors Complete and maintain documentation related to assigned work, including log books, batch records etc Act as a point of contact for a compliance audit Operate drum coater and compression equipment or roller compactors Dispenses ingredients for batches Perform MBR manufacturing batch report updates Perform manual handling of product - loads and unloads tablets Deliver on agreed KPIs and metrics Other duties as requested Requirements: Three years relevant industrial experience in a cGMP manufacturing environment A relevant level 6 qualification is an advantage A technical/ engineering qualification or background is an advantage Excellent written and spoken communication skills with established interpersonal skills Proficiency in MS applications Demonstrates strong safety orientation with strict adherence to established safety practices and standards Detail orientated A can-do attitude towards customer delivery and performance Why Join Catalyx? At Catalyx we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Catalyx benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities. Catalyx is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace where all individuals are valued, respected, and supported. We do not discriminate on the basis of race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. We encourage applications from all qualified candidates, regardless of background, and strive to create a welcoming environment for everyone. At Catalyx, we are committed to attracting the best global talent. We proudly support our international employees by offering assistance with Critical Skills Visa applications for eligible candidates. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

Manufacturing Technician - Thurles / Templemore My client has just launched a brand-new yeast production plant near Thurles/Templemore, transforming a dairy by-product into a sustainable, non-GMO animal feed. They're now looking for a Manufacturing Technician to join their growing team. This is a hands-on role where you'll play a key part in the day-to-day running of the facility and help shape the future of an exciting new venture. What You'll Be Doing (full training provided) Materials Handling - Receive, test, and manage raw materials and stock. Fermentation Runs - Operate and monitor yeast fermentation, including vessel setup, inoculation, controls, and cleaning. (Initially under close supervision until processes are fully refined). Process Monitoring - Record and track fermentation data to identify trends and improvements. Concentration - Operate, oversee, and clean the centrifuge used to concentrate fermented material. Drying & Bagging - Monitor drying, milling, and bagging of yeast biomass into powder. Cleaning - Utilise CIP skid to maintain high hygiene standards. Maintenance - Carry out routine maintenance tasks as required. Quality Assurance - Follow SOPs to meet quality, safety, and production standards. Collaboration - Share results, flag issues, and work closely with colleagues to keep things running smoothly. What We're Looking For Detail-focused with strong problem-solving skills. A flexible, positive communicator who enjoys learning new skills. Comfortable with shift work. Adaptable to changing priorities in a fast-moving environment. What's in It for You Salary up to €35K DOE. Be part of a start-up where your ideas and input truly count. Work within a flat structure and supportive, close-knit team. Ready to Apply? If you're looking for your next step as a Manufacturing Technician and want to be part of a ground-breaking start-up from day one apply now and help shape the future of sustainable food production! Skills: Tipperary Manufacturing Technician General Operative

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