Press Tab to Move to Skip to Content Link Select how often (in days) to receive an alert: Date: Oct 9, 2025 Location: Galway, G, IE Req ID: 129663 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway The Senior Manager, Global Quality for HealthTech is responsible for the global HealthTech quality team in Celestica Galway to establish and maintain a quality-first culture across worldwide manufacturing facilities. This involves managing a large global organization, collaborating with customers, suppliers, and partners, and ensuring compliance with regulatory requirements (FDA, ISO, ASQ, RAC).Significant experience with FDA certification processes is required. Detailed Description Strong relationship management and interpersonal skills. Proficiency in Microsoft Office for data analysis and reporting. Understanding of validation principles and testing procedures. Knowledge of FDA, ISO, RAC, and CQA regulations and standards. Willingness to travel internationally (15%+). Experience with FDA and regulatory inspections. In-depth knowledge of quality management systems and global compliance. Experience in the HealthTech industry. Global and multi-site leadership experience. Experience in driving cultural change for quality awareness. Typical Experience Experience: 10-12 years in quality management and related functions (Manufacturing Quality, Design Quality, Validation, Quality Assurance, Quality Systems). Minimum 5 years conducting quality audits. Typical Education Education: Degree in Engineering or Sciences required. RAC(US), CQA, ASQ, or ISO/RABSQA Auditor Certification is desirable. Notes This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time. Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law). At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them. COMPANY OVERVIEW: Celestica (NYSE, TSX: CLS) enables the world’s best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud.Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers. Celestica would like to thank all applicants, however, only qualified applicants will be contacted. Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services. #J-18808-Ljbffr
A global leader in manufacturing solutions is seeking a Manufacturing Engineer to optimize processes and enhance product quality in Galway. The candidate should have a degree in Engineering/Science and over 4 years of experience in process engineering, focusing on automated environments. This role emphasizes continuous improvement, collaboration, and problem-solving, with a competitive salary and growth opportunities. #J-18808-Ljbffr
A global tech solutions leader in Galway seeks a Director, Global Quality for HealthTech to lead quality initiatives across manufacturing facilities. The ideal candidate has over 10 years in quality management, with strong FDA compliance knowledge and experience in the HealthTech industry. This position requires significant travel and people management, supporting a quality-first culture across the organization. #J-18808-Ljbffr
A leading manufacturing solutions provider in Galway is seeking an experienced Automation Systems Engineer to oversee Factory Systems Infrastructure. This role involves managing high-speed automated production lines and requires a degree in Mechatronics or Automation with at least 2 years of relevant experience. Key responsibilities include system performance management and collaboration with the IT group for automation support. Competitive benefits and training opportunities are available. #J-18808-Ljbffr
Press Tab to Move to Skip to Content Link Date: Sep 30, 2025 Location: Galway, G, IE Req ID: 128905 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway Overview We are looking for a skilled Product Engineer to join our team. In this role, you will be primarily responsible for the management of our Bills of Materials (BOMs) and manufacturing routes. You will serve as the critical link between design and manufacturing, ensuring that all product data is accurate and enables efficient, high-quality production. You will also support teams like Engineering and Operations on key initiatives such as Design for Manufacturing (DFM) and Continuous Improvement (CI). Key Responsibilities Change Management: Manage the implementation of Engineering Change Orders (ECOs), updating product data across all relevant systems. Cross-functional collaboration: DFM: Partner with the Engineering team to ensure products are optimised for efficient and cost-effective manufacturing. Process Improvement: Support CI to identify and implement improvements to existing manufacturing processes to enhance quality, reduce costs, and increase efficiency. Problem Solving: Act as a technical expert to resolve production issues, conducting root cause analysis, and implementing corrective actions. Qualifications Proven experience as a Product Engineer, Manufacturing Engineer, or similar role. Strong knowledge of ERP systems (SAP experience is a plus) and MES systems (Spectrum Pro experience is a plus). Solid understanding of manufacturing processes and principles. Excellent problem-solving, communication, and collaboration skills. Familiarity with lean manufacturing and continuous improvement methodologies. Physical Demands Duties of this position are performed in a normal office environment. Duties may require extended periods of sitting and sustained visual concentration on a computer monitor or on numbers and other detailed data. Repetitive manual movements (e.g., data entry, using a computer mouse, using a calculator, etc.) are frequently required. Occasional travel may be required. Typical Experience 4 to 6 years of related experience. Typical Education Bachelor's degree in Mechanical Engineering, Industrial Engineering, or a related field. Educational Requirements may vary by Geography Notes This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time. Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law). At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them. COMPANY OVERVIEW: Celestica (NYSE, TSX: CLS) enables the world’s best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers. Celestica would like to thank all applicants, however, only qualified applicants will be contacted. Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services. #J-18808-Ljbffr
Overview Senior Lead Engineer, Manufacturing Process 1 1 1 Date: Sep 25, 2025 Location: Galway, G, IE Req ID: 128876 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway A career at Celestica is only for those who want to do something extraordinary with a meaningful purpose: imagine, develop and deliver a better future with our customers. Celestica is a leader in high – reliability design, manufacturing and supply chain solutions that bring global expertise to every stage of product development. By joining Celestica Galway (Ireland) as a Senior Lead Engineer, Manufacturing Process Engineer you will have the opportunity to work on delivering a fully automated high volume manufacturing line from development stage to full scale production ramp producing world class medical devices in a dynamic, fast moving environment. This position offers a great opportunity for a Senior Lead Engineer to work in a dynamic and challenging environment of high speed automation for micro assemblies across our business in the Automated Technology Solutions & Health-tech (Medical Device) market. Your next challenge will be… To become responsible for designing, developing, deploying and optimizing processes for manufacturing to achieve quality, cost and delivery goals for Celestica and its customer’s products. This role provides support and ongoing development to a complex high speed automated production line and new product introductions. This position will be responsible for supporting some of our product family in the ATS & Medical Device markets working closely with the operations, technical and quality teams and product designers to drive projects that continually improve the line performance as well as solution and provide input to new business opportunities. The position will report into our Engineering Manager. Your day to day activities will include the following… Being responsible for understanding and implementing the customer’s technical roadmap and related process development projects. Leading and implementing the development and release of the full manufacturing process for new customer products. Understanding and providing feedback on customer’s technical requirements to team members and management Developing and implementing costed and optimized feedback using Design for manufacturability (DFX) tools and processes, with the goal of reducing manufacturing cost and improving quality and reliability of product. Developing, planning and leading the assessment of the capability of process applications using the design of experiments. Devising process controls and data collection strategies and evaluating complex data to assist with reporting yield, reliability and diagnoses to root causes failures impacting product quality. Project Management - Ability to manage/lead complex, multiple line engineering projects that may also involve other functions. Demonstrate solid understanding of the technical, financial and people aspects of the project. Able to create a project/change management plan and ensure that the project is delivered within the assigned time and budget. Ability to recognize project barriers and develop mitigation plans Financial Acumen / Business Planning - Ability to create financial plans for your projects, align them internally with your line of management and other functions and externally if needed. Create project plans, profitability calculations, risk and sensitivity analysis, able to recognize barriers and mitigate profitability risks. Fully knowledgeable about internal and external financial reporting, accounting and tax requirements relevant to your area of expertise. The following competencies may also be required: Coaching/Mentoring; Communication/Negotiation/Presentation; Creative Problem Solving; Customer Interaction/Stakeholder Management; Quality & Lean; Working Effectively with Others; D/PFMEA; 8D/Corrective Action; Equipment Safety; Design of Experiments (DOE). NPI-PCBA: ESD, Component Prep, Laser marking, Solder Paste Deposition (screening / jetting) / Stencil Design, SMT component placement, Reflow, Tooling design, PTH soldering, PTH manual assembly, Press Fit assembly, Depanelization, Board level mechanical assembly, wire harness assembly, wire prep, SMT data analytics, SMT / PTH manual / automated rework, cleaning processes, coating / potting underfill / ruggedization processes, pack & ship, optical component assembly, fiber / tray handling processes, fiber splicing, IPC-610, quality data (KPI), Engineering Control & System Tools (ODC/SCE), Manufacturing Operational management, DFM - Mfg, DFA, DFR, Customer specific processes, structural test and inspection processes, machining, welding, CNC programming, secondary processes, sheet metal, DFAA. DFX: ESD Controls, Component Prep, Component Module Programming, Laser Marking, Screening, Solder Paste Dispense / Jetting, SMT Programming, SMT Placement, SMT Reflow, Sweat Soldering, Flex Board Assembly / Handling, Pallet Design, PTH Soldering, Robot Soldering, PTH manual Assembly, PTH Auto Assembly, Pressfit, Depanelization, Mechanical Assemb;y (TIMs, Heatsinks, PCBA, Hotbar, Ultrasonic Welding), Wire Harness Assembly, Wire Prep, System Assembly, SMT and PTH Rework, Cleaning Processes, Conformal Coating, Underfills / Edgebonding / Potting, Pack and Ship, Chassis Assembly (fluidics, electrical enclosure, cable routing), Sheet Metal , Machining, Welding, Structural Test (API, AOI, AXI, ICT, Flying Probe) FA LAB : ESD Controls, Solder Metallurgy, Strain Gauge Analysis, SIR Testing, Solder Joint Reliability Modeling, Sample Prep (Grind and Polish), Dye & Pry, CMM/VMM, Lab X-Ray, Pull/Bend Testing, Vibration Testing, Drop Testing, TDR, XRF, SEM, FTIR, IC, Solderability Testing, Thermal Analysis, HALT/HASS, TH&B, Thermal Shock, ATC OPTICAL & XRAY INSPECTION: ESD Controls, Auto Wire Prep, SMT Data Analytics, API, AOI (PCBA), AXI (PCBA), AOI (System), Test Strategy Creation, IPC-610, Quality Dat (KPI), DFM - Manufacturing, DFA - Assembly, DFT / Physical Test, DFT - Electrical Test MACHINING & OTHER: ESD Controls, Pack & Ship, CNC programming, Secondary Processing, Sheet Metal, Machining, Welding, DFM - Manufacturing MECHANICAL & SYSTEMS ASSEMBLY: ESD Controls, Wire Harness Assembly, Auto Wire Prep, Mechanical Assembly - System Build, OEE / Industrial Engineering, Pack & Ship, Vacuum System, Fluidics, Electrical Enclosure, Cable Routing, Electrical - Automation, Mechanical - Automation, Machine Vision, IPC-610, Engineering Controls, Quality Data (KPI), Manufacturing Operational Management, DFM - Manufacturing, DFA - Assembly, DFAA - Automated Assembly, DFT - Physical Test What do we offer? Market-competitive total reward: flexible salary, fix and variable salary based on goals The opportunity to become a key member of the new product introduction team in the Health Tech. Engineering function driven by innovation where creativity matters. Training and development opportunities, with us the sky is the limit! The opportunity to innovate, learn, mentor others and work toward your own vision of career success A global, collaborative culture with strong leadership imperatives to foster your growth and professional opportunities A sustainable culture where we provide opportunities for employees to give back to the community What do we expect from you? Excellent Project Management and Time Management skills Experience creating CAPA, FMEA, SOPs, Control Plans and performing validation (FAT, SAT, IQ, OQ, PQ). Ability to effectively communicate manufacturing plans, proposals, results, and negotiate options at management levels. Strong analytical and problem solving skills. Excellent interpersonal & communication skills. Strong report writing & data analytical capabilities. Advantageous to have knowledge of the medical device industry and of 21 CFR, (820, 11), ISO13485, specifically in the areas of Change Control and Validation. What are we looking for? Someone with a Degree in Engineering with 4+ years\' relevant experience Relevant Medical Device AND/OR Automation experience preferred Experience in ISO13485 medical device manufacturing environment is desirable. Relevant project management experience and associated qualifications with NPI experience Someone with an ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically and make sound decisions Someone that is open to the opportunity of short term travel assignments particularly at the early stages of the project. Someone that has excellent customer Management skills and a knowledge of customer and regulatory requirements. Someone that has previous experience of coaching and mentoring junior engineers. Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law). At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them. COMPANY OVERVIEW: Celestica (NYSE, TSX: CLS) enables the world’s best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers. Celestica would like to thank all applicants, however, only qualified applicants will be contacted. Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services. #J-18808-Ljbffr
Director, Global Quality Date: Sep 10, 2025 Location: Galway, G, IE Req ID: 128753 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway Job location: Ireland, Galway. Reporting to Celestica's Vice President of Global Quality, the Director, Global Quality for HealthTech is responsible for the global HealthTech quality team to establish and maintain a quality-first culture across worldwide manufacturing facilities. This involves managing a large global organization, collaborating with customers, suppliers, and partners, and ensuring compliance with regulatory requirements (FDA, ISO, ASQ, RAC). Significant experience with FDA certification processes is required. Responsibilities Strong relationship management and interpersonal skills. Proficiency in Microsoft Office for data analysis and reporting. Understanding of validation principles and testing procedures. Knowledge of FDA, ISO, RAC, and CQA regulations and standards. Willingness to travel internationally (60%+). Typical Experience 10-12 years in quality management and related functions (Manufacturing Quality, Design Quality, Validation, Quality Assurance, Quality Systems). Minimum 5 years conducting quality audits. Experience with FDA and regulatory inspections. In-depth knowledge of quality management systems and global compliance. Experience in the HealthTech industry. Global and multi-site leadership experience. Experience in driving cultural change for quality awareness Notes This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time. Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law). At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them. COMPANY OVERVIEW: Celestica (NYSE, TSX: CLS) enables the world’s best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud.Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers. Celestica would like to thank all applicants, however, only qualified applicants will be contacted. Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services. #J-18808-Ljbffr
A global technology solutions provider located in Galway, Ireland is seeking a Lead Engineer in Manufacturing Process. The role involves leading process development and continuous improvement in high-speed automated manufacturing environments. Candidates should have over 4 years of experience in process engineering, strong leadership skills, and familiarity with ISO13485 regulations. The position offers a competitive salary and opportunities for professional growth. #J-18808-Ljbffr
Location: Galway, G, IE Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway Functional Area: Engineering Career Stream: Design Engineering Systems Applications SAP Short Name: ENG-ENG-DSA Job Level: Level 07 IC/MGR: Individual Contributor Direct/Indirect Indicator: Indirect Summary Who we are and what we do? Celestica Galway are a leader in automated manufacturing services with proven expertise in delivering scalable manufacturing solutions throughout the product lifecycle. Celestica Galway supports and provides Automated Technology Solutions & Health-tech Solutions for a number of customers including the Medical Device space. Your next challenge will be… Celestica Galway site is now recruiting for an experienced Automation Systems Engineer to plan, implement and maintain a comprehensive Factory Systems Infrastructure, which is in line with corporate guidelines and customer requirements in order to facilitate a world-class manufacturing environment. This role provides support and ongoing development to a number of high speed automated production lines and new product introductions, in particular paying attention to PLC controlled equipment, vision systems, robotics and manufacturing data integrity & security. This position involves working shifts. Shift patterns are as follows: A Shift: Monday, Tuesday, Wednesday and every second Sunday: 7:30 AM - 7:30 PM B Shift: Sunday, Monday, Tuesday and every second Saturday night: 7:30 PM - 7:30 AM C Shift: Thursday, Friday, Saturday and every second Sunday: 7:30 AM - 7:30 PM D Shift: Wednesday, Thursday, Friday and every second Saturday night: 7:30 PM - 7:30 AM Detailed Description Your day-to-day activities will include the following… Performs tasks such as, but not limited to, the following: Proactively manages and supports the existing Automation infrastructure for optimal performance and minimized downtime. Makes appropriate, justifiable suggestions for system enhancements. Systems include: Allen Bradley PLC’s and associated Rockwell applications, ASI/ControlNet/Data Highway Bus systems, Cognex Systems, Servo systems and Allen Bradley PanelViews SE; Collaborates with the IT Group, Application Group, and External Technical Resources to provide comprehensive support of all Automation and Information Systems and Technologies; Provide technical support to all control system related issues; Provides solutions, which implement industry best practice to deliver improved productivity and efficiency throughout the organization; Installs and deploys systems, software and peripherals as required, liaising with external vendors and service contractors as appropriate. Sources appropriate equipment and services through appropriate liaison with the purchasing department; Provides Technical Direction for all new infrastructure developments; Develops, implements and manages comprehensive contingency plans for all critical systems including regular documented tests; Benchmarks system performance and provides regular reports; Interfaces with Corporate Information Systems on standards, support, and new infrastructure developments; Utilizes a Project Management methodology to plan, coordinate and implement Key projects assigned by Business Unit Managers. Provides regular reports to Management and delivers projects within agreed time-frames and budgets; Documentation is a key function of any Engineering professional: all knowledge is to be captured and shared as the fundamental aspect of system support; all procedures must be written and controlled to ISO standards; Utilizes Continuous Process Improvement methodologies to improve the overall quality of all systems you come into contact with; All other duties/responsibilities as defined by the Engineering Manager; Develops training programmes for our Capital systems Technician line support; Provides innovative inputs to new production lines in the areas of control, data collection, motive power, robotics, vision systems and communications; Develop and implement process improvements on new and existing lines. What do we expect from you? Good presentation skills and ability to deliver training courses when necessary; Facilitation skills and a sound understanding of team dynamics; A motivated individual with focus and discipline; An achievement oriented self-starter with excellent problem solving skills; What are we looking for? A Degree in Mechatronics or Automation discipline with 2+ year’s relevant experience; Experience in ISO13485 medical device manufacturing environment is desirable; Experience in a highly automated manufacturing environment and with highly automated equipment is desirable; Experience with GDP & GMP (Good Documentation Practices & Good Manufacturing Practices); Experience in GAMP, 21 CFR Part 11 environments; Good understanding of Electrical & Pneumatic Panel drawings; Experience desirable but not essential with VB code development and generation; Experience in Allen Bradley PLC platforms to include Control Logix, Studio 5000 from a troubleshooting point of view; Experience desirable with Rockwell Software applications to include Factory Talk and Transaction packages; Essential experience required with network topology, pc application software, systematic troubleshooting/problem solving skills; Previous experience of TCP/IP and Wide Area Network architectures Relevant Medical Device AND/OR Automation experience preferred Software development (Visual Basic, C++); Equipment and Software Validation, IQ, OQ and PQ; Excellent problem-solving skills and attention to detail; Physical Demands Duties of this position are performed in a normal office environment. Duties may require extended periods of sitting and sustained visual concentration on a computer monitor or on numbers and other detailed data. Repetitive manual movements (e.g., data entry, using a computer mouse, using a calculator, etc.) are frequently required. Occasional travel may be required. Typical Education Bachelor's degree in Mechatronics or Automation Educational Requirements may vary by Geography Notes This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time. Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law). At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them. COMPANY OVERVIEW: Celestica (NYSE, TSX: CLS) enables the world’s best brands. Through our recognized customer‑centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full‑scale production and after‑market services for products from advanced medical devices, to highly engineered aviation systems, to next‑generation hardware platform solutions for the Cloud.Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers. Celestica would like to thank all applicants, however, only qualified applicants will be contacted. Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services. #J-18808-Ljbffr
Manufacturing Engineer - Shift Date: Oct 24, 2025 Location: Galway, G, IE Summary AShift: Monday, Tuesday, Wednesday and every second Sunday: 8 AM - 8 PM BShift: Sunday, Monday, Tuesday and every second Saturday night: 8 PM - 8 AM CShift: Thursday, Friday, Saturday and every second Sunday: 8 AM - 8 PM DShift: Wednesday, Thursday, Friday and every second Saturday night: 8 PM - 8 AM Your day-to-day activities will include the following… Create, execute, coordinate, and support the design of experiments, test methods, protocols, specifications, and validation documentation (IQ/OQ/PQ) and oversee the development and execution of qualification trials/characterization studies. Oversee and analyze the performance of equipment, vision systems and machines, optimizing process parameters to eliminate non-conforming products, low yields, or product quality issues. Champion and drive continuous improvement processes for production areas using structured Process Capability and Lean Six Sigma methodologies, leading cross-functional teams in these initiatives. Manage multiple projects, generate comprehensive project plans, and support as a team player project teams to drive completion and success, ensuring alignment with strategic objectives. Support the maintenance and calibration of critical equipment-systems, ensuring compliance and optimizing maintenance schedules. Work with cross-functional teams and external vendors to integrate new products, processes, and technologies into the existing manufacturing area, leading the technology transfer and implementation. Detailed Description Performs tasks such as, but not limited to, the following: Design, develop, and implement new manufacturing processes to support customer products. Develop application software and tooling for a series of complex machines and mechanical process steps within a manufacturing sector. Execute with support, capability of machines and process steps using Design of Experiments and statistical methods to ensure maximum utilization of critical resources, maximum throughput, minimum cost and capacity growth; involves integrating equipment, people, material flow, and information systems. Solve technical product, process, component, and related problems that affect the efficient operation and/or manufacture of products. Provide feedback to product designers on suitability of designs for manufacturability with supervision. What do we expect from you? Experience using engineering tools and software packages to support automated manufacturing processes. Proven experience in detailed analysis, modelling, and methodologies to validate manufacturing process and tooling design and specifications. Experience in creating SOP’s, Control Plans, and performing validation (FAT, SAT, IQ, OQ, PQ). Demonstrated ability to effectively communicate manufacturing plans, proposals, and results, and negotiate options at executive management levels. Experience in analytical and problem-solving skills. Excellent interpersonal and communication skills. A strong aptitude for report writing and data analytics. An advantage with knowledge of the medical device industry and of 21 CFR, (820, 11), ISO13485, specifically in the areas of Change Control and Validation. What are we looking for? A minimum of 4+ years’ experience in a Process Engineering role, with a proven track record of involvement in projects and teams. A Primary Degree in an Engineering/Science discipline. Medical Device AND/OR Automation experience an advantage. Experience in a highly automated manufacturing environment. An ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically, and make sound decisions. What do we offer? Market-competitive total reward: flexible salary, fixed and variable salary based on goals. The opportunity to work with new product introduction teams in the Health Tech sector. Engineering Function driven by innovation where creativity matters. Training and development opportunities; with us, the sky is the limit! The opportunity to innovate, learn, mentor others, and work toward your own vision of career success. A global, collaborative culture with strong leadership imperatives to foster your growth and professional opportunities. A sustainable culture where we provide opportunities for employees to give back to the community. Notes This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time. Equal Employment Opportunity Statement Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law). At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them. Company Overview Celestica (NYSE, TSX: CLS) enables the world’s best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers. Celestica would like to thank all applicants, however, only qualified applicants will be contacted. Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services. #J-18808-Ljbffr
