Overview Join to apply for the Manufacturing Engineer - Shift A role at Celestica Req ID: 129050 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway General Overview Functional Area: Engineering Career Stream: Process Engineering Manufacturing SAP Short Name: ENG-ENG-PRM Job Level: Level 07 IC/MGR: Individual Contributor Direct/Indirect Indicator: Indirect Summary Great opportunity to join us as Shift Engineer: A Shift: Monday, Tuesday, Wednesday and every second Sunday: 8 AM - 8 PM 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. Knowledge/Skills/Competencies 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 SOPs, 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, fix 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. 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. Seniority level Mid-Senior level Employment type Full-time Job function Engineering and Information Technology Industries Notes on referrals and job postings omitted for brevity. #J-18808-Ljbffr
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 BOM & Route Management: Create and maintain accurate BOMs and manufacturing routes for all products. Ensure the seamless transfer and synchronisation of data between core systems, such as Enterprise Resource Planning (ERP) (SAP) and Manufacturing Execution Systems (MES) (Spectrum Pro) to guide shop floor operations. Master Data Accuracy and Integrity: Ensure the accuracy, completeness, and consistency of all product master data, including BOMs and routes. This is critical for maintaining a single source of truth across all systems and for enabling effective planning, costing, and production. 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. Knowledge/Skills/Competencies 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 methods. 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 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. 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. 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 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 is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status. 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. #J-18808-Ljbffr
Senior Lead Engineer, Manufacturing Process 1 1 1 Join to apply for the Senior Lead Engineer, Manufacturing Process 1 1 1 role at Celestica Req ID: 128876 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway A career at Celestica is 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 to work in the 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. Enabling Competencies 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 Leadership - Demonstrate "People & Team Leadership Behaviours" as per Celestica Leadership Imperatives. 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). Technical Competencies 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 ly (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 MICROELECTRONICS: ESD Controls, Wafer Thinning, Wafer Singulation, Edge Polishing, Optical Coatings, Die Bonding, Vacuum Reflow, Flip Chip Bonding, Underfill, Active Alignment, Plasma Cleaning, Wire Bonding, Encapsulation, Sealing, Leak Testing, Interconnect Formation 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 What do we expect from you? Excellent Project Management and Time Management skills Excellent communication Skills both written and verbal. Experience creating CAPA, FMEA, SOP’s, 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. 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. Headquartered in Toronto, with 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 thanks all applicants, however, only qualified applicants will be contacted. Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services. Seniority level: Mid-Senior level Employment type: Full-time Job function: Engineering and Information Technology Industries: Manufacturing Note: This description has been refined for formatting clarity; no substantive job information was altered. #J-18808-Ljbffr
Overview Job location: Ireland, Galway. Reports 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, collaborating with customers, suppliers, and partners, and ensuring regulatory compliance (FDA, ISO, ASQ, RAC). Significant experience with FDA certification processes is required. This role involves leading a large global organization, driving operational excellence, and delivering results in a complex and dynamic environment. Responsibilities Develop and implement the global quality strategy in collaboration with regional and site leadership, identifying gaps and creating short- and long-term plans. Share best practices across HealthTech teams and host quality forums for issue discussion, decision-making, and plan execution. Establish the HealthTech Quality Strategy (e.g., MDSAP / MDR). Define annual quality objectives and metrics aligned with business priorities, driving quality culture and performance improvements. Oversee the quality management system globally, including industry certifications, customer surveys, operational reviews, and system applications. Cultivate an "audit-ready" culture and direct the Global Regulatory Compliance Audit Program, ensuring internal audits are effective and findings are tracked to closure. Conduct Quality Management Reviews and training with manufacturing sites and executive management, advising on risks and mitigation plans. Maintain an effective 8D reporting system for quality issues and resolutions, involving crossfunctional staff. Manage talent within the Quality team, including hiring and training. Provide program management leadership for special projects and initiatives and guide quality communities and internal teams. Knowledge/Skills/Competencies 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%+). Experience & Qualifications 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 company located in Galway is seeking a Director, Global Quality for HealthTech. The role involves leading the quality team to establish a quality-first culture, ensure regulatory compliance, and drive operational excellence. Candidates should have extensive experience in quality management, particularly with FDA certifications, and strong leadership skills. The position requires international travel up to 60%. #J-18808-Ljbffr
Lead Engineer, Manufacturing Process – Celestica, Galway, Ireland Req ID: 129357. Remote Position: No. Region: Europe. Country: Ireland. State/Province: Galway. City: Galway. Summary A career at Celestica is 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. As a Lead Manufacturing Process Engineer, you will lead the development and implementation of fully automated high‑volume manufacturing lines from development stage to full‑scale production ramp, producing world‑class medical devices in a dynamic, fast‑moving environment. Key Responsibilities Lead and be accountable for process development, troubleshooting, and continuous improvement of the production process and equipment in the manufacturing area; strategic planning and optimization of manufacturing processes. Collaborate with operations, technical & quality teams, and Product Designers to lead and drive complex projects that improve line performance, provide innovative solutions, and contribute to new business opportunities; mentor and guide other engineers. Lead the process engineering activities for one or more product families in the ATS & Medical Device markets; liaise with Production, Engineering, Supply Chain and Customer contracts; report to Engineering Manager. Oversee and analyze performance of equipment, machines, and tools using advanced statistical methodologies to resolve complex equipment issues and optimize 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. Create, execute, coordinate, and lead 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. Manage multiple complex projects, generate comprehensive project plans, and lead project teams to drive completion and success, ensuring alignment with strategic objectives. Oversee maintenance and calibration of critical equipment‑systems, ensuring compliance and optimizing maintenance schedules. Interface 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. Lead the development of automated solutions for NPI programs, including new business development opportunities, and provide strategic input on automation strategies. Oversee and approve the qualification of engineering change management, ensuring robust change control processes. Mentor and provide technical guidance to other process engineers, fostering their development and growth. Required Qualifications Extensive experience using engineering tools and software packages to design and automate complex manufacturing processes. Proven experience in detailed analysis, modeling, and methodologies to validate manufacturing process and tooling design and specifications. Extensive experience in creating CAPA, FMEA, SOPs, Control Plans, and performing validation (FAT, SAT, IQ, OQ, PQ). Demonstrated ability to communicate manufacturing plans, proposals, and results effectively, and negotiate options at the executive management level. Exceptional analytical and problem‑solving skills. Excellent interpersonal and communication skills. Strong aptitude for report writing and data analytics. In‑depth knowledge of the medical device industry and of 21 CFR, (820, 11), ISO 13485, specifically in the areas of Change Control and Validation. Experience A minimum of 4 + years’ experience in a Process Engineering role with a proven track record of leading projects and teams. A primary degree in an Engineering/Science discipline; a Master’s degree is preferred. Medical Device and/or Automation experience is essential. Extensive experience in an ISO 13485 medical device manufacturing environment. Extensive experience in a highly automated manufacturing environment. A strong leader who can initiate and lead change, collaborate and create alignment, drive accountability, think critically, and make sound decisions. Open to short‑term travel assignments, particularly at the early stages of the project. Benefits Market‑competitive total reward: flexible salary, fixed and variable salary based on goals. Opportunity to lead 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. Opportunity to innovate, learn, mentor others, and work toward your own vision of career success. A global, collaborative culture with strong leadership that fosters your growth and professional opportunities. A sustainable culture where we provide opportunities for employees to give back to the community. 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, 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. EEO 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. Celestica does not accept unsolicited resumes from recruitment agencies or fee‑based recruitment services. #J-18808-Ljbffr
