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. 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, Stencil Design, 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 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 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 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 DeviceAND/ORAutomation 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. To Apply Please forward your CV via the APPLY Now button below.
Req ID: 130085 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway General Overview 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 enables the world's best brands. Through our unrivalled customer-centric approach, we partner with leading companies in aerospace and defence, communications, enterprise, health-tech, industrial, capital equipment, and smart energy to deliver solutions for their most complex challenges. With talented teams across North America, Europe and Asia, we imagine, develop and deliver a better future with our customers. 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 experiencedAutomation 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. Knowledge/Skills/Competencies What do we expect from you? Excellent Project Management skills; 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 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. To Apply Please forward your CV via the APPLY Now button below.
04 - Operations Engineering Support 1 Req ID: 129776 Remote Position: No Hiring Manager: Joseph Patrick Callanan Band: 04 Region: Europe Country: Ireland State/Province: Galway City: Galway Summary Graduate Manufacturing Technician (Automation & Robotics Focus) - Kickstart Your Career in Automation & Robotics with Celestica Galway! Imagine, develop, and deliver a better future - that's what we do at Celestica! We're a global leader in technology solutions, partnering with the world's best brands to bring their products to life. Calling all graduates with a passion for automation and robotics! Join our team in Galway, Ireland as a Manufacturing Technician Graduate and gain hands-on experience in a cutting-edge manufacturing environment. You'll be a key member of our team, working on exciting projects related to automation, robotics, and advanced manufacturing processes. This position involves a working week of 42 hours. You will be placed on a day shift. Detailed Description What you'll do: Hands-on experience: Work directly with robots, automated systems, and cutting-edge technology. Troubleshooting and maintenance: Assist in troubleshooting and maintaining automated equipment, including robotic systems. Process improvement: Contribute to the improvement of our manufacturing processes, focusing on automation and robotics. Programming and control: Gain experience in programming and controlling robotic systems. Data analysis: Collect and analyze data to optimize the performance of automated systems. Collaboration: Work closely with engineers and technicians to implement and improve automated solutions. What you'll gain: Real-world application: Apply your knowledge of automation and robotics in a real-world manufacturing setting. Skill development: Enhance your technical skills in robotics, automation, programming, and problem-solving. Mentorship and collaboration: Learn from experienced professionals and contribute to a dynamic team. Career growth: This graduate position could be your launchpad to a rewarding career in automation and robotic Knowledge/Skills/Competencies Who you are: Technically minded: You have a strong foundation in automation and robotics principles. Hands-on learner: You enjoy working with technology and applying your knowledge to solve problems. Team player: You thrive in a collaborative environment and enjoy working with others. Eager to learn: You're passionate about automation and robotics and excited to gain practical experience. Support and Development: You will be supported by a team of experienced engineers and have access to structured training programmes, upskilling opportunities, and ongoing professional development. As your skills and confidence grow, you'll take on increased ownership and responsibility, contributing directly to key engineering activities. Ready to turn your classroom knowledge into real-world experience?Apply now! Typical Education Recently graduated with a qualification in Automation, Robotics, Mechatronics, or a related field. 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. To Apply Please forward your CV via the APPLY Now button below.
04 - Operations Engineering Support 1 Req ID: 129778 Remote Position: No Hiring Manager: Joseph Patrick Callanan Band: 04 Region: Europe Country: Ireland State/Province: Galway City: Galway Summary Student Co-op Manufacturing Technician (Automation & Robotics Focus) - Launch Your Career in Automation & Robotics with Celestica Galway! Imagine, develop, and deliver a better future - that's what we do at Celestica! We're a global leader in technology solutions, partnering with the world's best brands to bring their products to life. Calling all co- ops students with a passion for automation and robotics! Join our team in Galway, Ireland as a Student Co-op Manufacturing Technician (Automation & Robotics Focus)! This is your chance to gain valuable hands-on experience in a cutting-edge manufacturing environment. You'll be a key member of our team, working on exciting projects related to automation, robotics, and advanced manufacturing processes. This position involves a working week of 42 hours. You will be placed on a day shift. Detailed Description What you'll do: Hands-on experience: Work directly with robots, automated systems, and cutting-edge technology. Troubleshooting and maintenance: Assist in troubleshooting and maintaining automated equipment, including robotic systems. Process improvement: Contribute to the improvement of our manufacturing processes, focusing on automation and robotics. Programming and control: Gain experience in programming and controlling robotic systems. Data analysis: Collect and analyze data to optimize the performance of automated systems. Collaboration: Work closely with engineers and technicians to implement and improve automated solutions. What you'll gain: Real-world application: Apply your knowledge of automation and robotics in a real-world manufacturing setting. Skill development: Enhance your technical skills in robotics, automation, programming, and problem-solving. Mentorship and collaboration: Learn from experienced professionals and contribute to a dynamic team. Career growth: This co-op placement could be your launchpad to a rewarding career in automation and robotics. Knowledge/Skills/Competencies Who you are: Technically minded : You have a strong foundation in automation and robotics principles. Hands-on learner : You enjoy working with technology and applying your knowledge to solve problems. Team player : You thrive in a collaborative environment and enjoy working with others. Eager to learn : You're passionate about automation and robotics and excited to gain new skills and knowledge in a dynamic environment. Support and Development : You will be supported by a team of experienced engineers and have access to structured training programmes, upskilling opportunities and ongoing professional development. Ready to launch your career in advanced manufacturing? Apply now! 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. To Apply Please forward your CV via the APPLY Now button below.
Req ID: 129930 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway General Overview Functional Area: ENG - Engineering Career Stream: OPE - Operations Engineering Role: Technical Support 2 SAP Short Name: TS2 Job Title: Operations Engineering Support 2 Job Code: TS2-ENG-OPS Job Level: Band 05 Direct/Indirect Indicator: Direct Summary Installation, set up, maintenance and support of automated equipment ensuring optimum performance and achieving operational goals. This will include providing factory systems support in a highly automated production environment while also Implementing continuous improvement solutions to maximize equipment efficiency and robustness. Detailed Description Your day-to-day activities will include the following... Repairing and troubleshooting high speed automated assembly machines Scheduling and performing preventative maintenance procedures Helping to move, install, set-up and refurbish equipment Maintaining accurate and up-to-date maintenance documentation Communicating potential problems that may affect capacity and quality to the business unit Team Leader as well as across zones/work areas where necessary Supporting Process Engineers to ensure continuous improvements are ongoing Contributing to efficiency improvement projects through code upgrades Meeting performance targets and production deadlines Working proactively on your own initiative with minimal supervision Knowledge/Skills/Competencies Strong knowledge of the setup, operation, and maintenance of specific equipment sets used in manufacturing processes. An ability to demonstrate advanced thinking and logical approach to problem solving An ability to demonstrate a high level of technical ability, with hands on approach to solving technical issues Good interpersonal skills and ability to work as part of a team Someone who is Resourceful, hands-on and enjoys a challenge Knowledge of robotics, vision system and debugs analysis Good analytical skills Good risk assessment methodology Typical Experience 2+ years of experience as a technician in a high-volume automated environment Experience in Medical Devices or suppliers Knowledge of Allen Bradley PLC devices is an advantage Knowledge of electrical systems Typical Education Minimum Level 5 qualification within an engineering discipline or trade equivalent in electronics/mechanics 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 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. To Apply Please forward your CV via the APPLY Now button below.
05 - Operations Engineering Support 2 1 Req ID: 128005 Remote Position: No Hiring Manager: Caroline Scully Band: 05 Region: Europe Country: Ireland State/Province: Galway City: Galway General Overview Functional Area: ENG - Engineering Career Stream: OPE - Operations Engineering Role: Technical Support 2 SAP Short Name: TS2 Job Title: Operations Engineering Support 2 Job Code: TS2-ENG-OPS Job Level: Band 05 Direct/Indirect Indicator: Direct Summary The Equipment Maintenance Technician is responsible for the set-up, installation, maintenance and support of automated equipment ensuring optimum performance and the achievement of operational goals. The Equipment Maintenance Technician works closely with teams to resolve manufacturing issues and constraints while implementing safe and robust solutions to improve overall efficiency through improvement projects around run rate increase, cycle time gains, yields and quality. This position for the day 8 AM - 8 PM Days. This position will report to the Team Leader. Detailed Description Repairs and troubleshoots electro/mechanical equipment failures. Schedules and performs preventative maintenance procedures. Helps move, install, set-up and refurbish equipment. Maintains accurate and up-to-date maintenance documentation. Records significant downtime issues and resolutions in appropriate databases. Interacts with other departments as required to co-ordinate equipment repairs. Works proactively to ensure performance targets are met; Yield/quality (using SPC/SQC)/production outs/up-time /process stability. Communicates potential problems that may affect capacity and quality to the Business Unit Team Leader as well as across zones/work areas where necessary. Attends pass-downs as required and provides status updates. Provides detailed inputs into failed spare parts management process. Supports Process Engineers to ensure Continuous Improvements are ongoing. Trains and assists other Technicians and Operators. Knowledge/Skills/Competencies Strong knowledge of the setup, operation, and maintenance of specific equipment sets used in manufacturing processes. Strong troubleshooting/Problem solving skills. Demonstrates a high level of technical ability, with hands on approach to solving technical issues. Excellent written and verbal communication skills. Good interpersonal skills and ability to work as part of a team. Commitment to achievement of manufacturing excellence. High level of flexibility: shift changes / training courses / preventative maintenance and Project support. Ability to work on own initiative, is self-driven. Resourceful, hands-on, enjoys a challenge. Works well under pressure. Typical Experience 2 - 4 years+ experience as a Technician in a high volume automated environment. Minimum Cert./Diploma/Senior Trades in Electrical/Mechanical Engineering or equivalent. Working knowledge of PLCs, Motor drives, pneumatic and hydraulic components is an advantage. 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. To Apply Please forward your CV via the APPLY Now button below.
04 - Process/Test Engineering Support 1 Req ID: 129931 Remote Position: No Hiring Manager: Ray O'Hara Band: 04 Region: Europe Country: Ireland State/Province: Galway City: Galway General Overview Functional Area: ENG - Engineering Career Stream: DEV - Process/Test Development Role: Technical Support 1 SAP Short Name: TS1 Job Title: Process/Test Engineering Support 1 Job Code: TS1-ENG-PROC Job Level: Band 04 Direct/Indirect Indicator: Indirect Summary Co-op System Engineer - Launch Your Career in Health Tech with Celestica Galway! Imagine, develop, and deliver a better future - that's what we do at Celestica! We're a global leader in technology solutions, partnering with the world's best brands to bring their products to life. Join our team in Galway, Ireland as a Co-op System Engineer and make a real impact in the exciting world of health tech! This is your chance to kick-start your career in a dynamic and innovative environment. You'll be a key member of our team, supporting cutting-edge automated production lines and contributing to the development of life-changing medical technologies. Detailed Description What you'll do: Support and optimize: Ensure the smooth operation of our factory systems infrastructure, including PLC-controlled equipment, vision systems, and more. Enhance and improve: Contribute to the development of new solutions and implement industry best practices to increase productivity and efficiency. Collaborate and innovate: Work closely with IT, application teams, and external partners to support and enhance our automation systems. Problem-solve and troubleshoot: Identify and resolve technical issues to minimize downtime and ensure optimal performance. New product launches: Play a key role in supporting the launch of new products and production lines. What you'll gain: Real-world experience: Gain practical experience in a high-tech manufacturing environment focused on health tech. Mentorship and collaboration: Work alongside experienced professionals and learn from the best in the industry. Skill development: Develop your technical skills in automation, robotics, vision systems, and more. Career growth: This graduate role could be your stepping stone to a rewarding career at Celestica. Knowledge/Skills/Competencies Who you are: Technically minded: You have a strong foundation in computer engineering, electronics, IT, or a related technology discipline. Creative problem-solver: You enjoy finding innovative solutions to technical challenges. Team player: You thrive in a collaborative environment and enjoy working with others. Eager to learn: You're passionate about technology and excited to contribute to the health tech industry. Qualifications: Bachelor's degree in Computer Engineering, Electronic, IT, or a related Technology discipline. Ready to launch your career in health tech? Apply now! 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. To Apply Please forward your CV via the APPLY Now button below.
Req ID: 129357 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: LEN-ENG-PRM Job Level: Level 08 IC/MGR: Individual Contributor Direct/Indirect Indicator: Indirect Summary 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 Lead Manufacturing Process Engineer, you will have the opportunity to lead the development and implementation of fully automated high-volume manufacturing lines from the 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 Lead Process Engineer to excel in a 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 lead and be accountable for process development, troubleshooting, and continuous improvement of the production process and equipment in the manufacturing area. This includes strategic planning and optimization of manufacturing processes. You will work closely with operations, technical & quality teams, and Product Designers to lead and drive complex projects that significantly improve line performance, provide innovative solutions, and contribute to new business opportunities. You will also be expected to mentor and guide other engineers within the team. This position will be responsible for leading the process engineering activities for one or more product families in the ATS & Medical Device markets, liaising with Production, Engineering, Supply Chain and Customer contracts, and reporting to our Engineering Manager. Detailed Description Your day-to-day activities will include the following... Oversee and analyze the 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 in these initiatives. 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 the 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. Knowledge/Skills/Competencies What do we expect from you? 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, 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. Exceptional analytical and problem-solving skills. Excellent interpersonal and communication skills. A strong aptitude for report writing and data analytics. In-depth 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 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 ISO13485 medical device manufacturing environment. Extensive experience in a highly automated manufacturing environment. A strong leader with the ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically, and make sound decisions. Someone who is open to the opportunity of short-term travel assignments, particularly at the early stages of the project. What do we offer? Market-competitive total reward: flexible salary, fix and variable salary based on goals The 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! 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 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. To Apply Please forward your CV via the APPLY Now button below.
Req ID: 129954 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway Summary Lead our quality assurance team as a Quality System Manager. We are hiring a Medical Device expert to own our QMS strategy and ensure flawless global compliance (FDA, ISO). This is a high-impact, mission-critical role based in Galway. Detailed Description Our next challenge will be to... Develop and implement a comprehensive quality strategy aligned with the company's long-term goals. Oversee the quality management system for site, including industry certifications Define annual quality objectives and metrics aligned with business priorities, driving quality culture and performance improvements. Cultivate an "audit-ready" culture for the site by participating in the Global Regulatory Compliance Audit Program. Ensuring internal audits are effective and findings are tracked to closure. Maintain an effective 8D reporting system for quality issues and resolutions, involving cross-functional staff. Provide program management leadership for special projects and initiatives and guide quality communities and internal teams. Lead Quality Improvement Programs (QIP) in support of customer requirements and expectations Direct and influence the preparation of documentation to support high quality regulatory submission dossiers. Act as the sites primary representative for all quality system related matters, ensuring compliance with QSR, FDA, ISO, and other pertinent regulations Act as company representative, developing and maintaining positive relationships with the Customer through oral and written communications. Manage with the customer the submission strategy/regulatory pathway and follow-up of any submissions under review. Mentors and trains personnel in the practices of Quality management and Quality improvement (succession development) 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 management team in the Health Tech business 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. Knowledge/Skills/Competencies Strong relationship management and interpersonal skills In depth knowledge of FDA, ISO, RAC, and CQA regulations and standards. Experience with FDA and regulatory inspections In-depth knowledge of quality management systems and global compliance. Experience in the Medical device industry Ability to effectively, communicate with a wide variety of internal and external customers. Ability to effectively lead, manage, train and motivate a diverse group of employees Ability to use some or all of the following PC applications: Google Applications, Word, Excel, and PowerPoint. Typical Experience Minimum of 7-10 years' experience in a Quality role 2 - 5+ years regulatory affairs experience or related experience in medical device industry and/or Pharmaceuticals is required. Working knowledge of FDA and international regulations Experience working directly with FDA, notified bodies and/or international health authorities is desired. Typical Education Degree qualifications (NQF L8 or L9) minimum in a related field 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 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. To Apply Please forward your CV via the APPLY Now button below.
Req ID: 129565 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway Summary 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. By Joining Celestica Galway (Ireland) as a Quality Engineer you will have the opportunity to work with an incredible team taking on the amazing challenge of becoming an emerging leader in the introduction of new Medical Device products. You will become responsible for dealing with the three major phases of Quality Management, Quality Planning/Prevention, Corrective Action. Your next challenge will be... Lead process/procedure definition and maintain a continuous flow of high-quality products to our customers in a contract manufacturing environment including regulatory content for the latest and more innovative medical devices. This position will be responsible for supporting some of our product family in both the Med tech and Industrial sectors liaising with Production, Engineering, Supply Chain and Customer contracts reporting into our Quality Manager. Detailed Description Your day- to-day activities will include: Mentors and develop personnel in the practices of Quality management and Quality improvement Lead the team to investigate any quality excursions and implement corrections and corrective actions Lead the quality group in a fast-paced production environment Customer liaison for quality escalations and daily quality issues ensuring measured, developed and timely responses to the customer. Support the change management process and Customer requests as appropriate. High level of competence using relevant corrective action systems (e.g CAPA) Create concise and accurate technical reports, communicate results and manage subsequent analysis queries Continually seek to drive improvements in product and process quality. Create and evaluate metrics to drive the quality improvement processes. Own, Maintain and report timely and accurate KPI's Manage and maintain the NCMR database and report weekly to the customer. Using appropriate statistical techniques to monitor process performance (e.g.SPC, Minitab, Ppk, Gage R & R analysis, sampling techniques). Provide quality engineering support to the facility, including validation and risk management and review of technical documentation (eg. FMEA's, control plans). Apply project management skills and methodology as necessary for key CI projects. Knowledge/Skills/Competencies What do we expect from you? Strong knowledge of quality tools, ISO / QMS standards and processes (ISO 9001, ISO13485) Knowledge of data analysis and presentation software and its uses in generating reports, capturing data and presenting data in an understandable format. Strong knowledge of product and manufacturing processes and materials properties Knowledge and understanding of the manufacturing environment and how decisions impact customer satisfaction product quality, on-time delivery and profitability of the unit Knowledge of quality tools such as FMEA, PMP, SPC, 8D methodology, etc. Knowledge of Six sigma and Lean Kaizen. Ability to effectively communicate with a wide variety of internal and external customers to summarize complex technical issues Knowledge of Med-tech and regulatory requirements (such as FDA and MDR) is a requirement of the role with pharma & medical device systems an advantage Ability to effectively lead and manage several projects simultaneously and coordinate multiple, changing deadlines while also working effectively on their own and in a team environment. Ability to be an Internal Auditor What are we looking for? Experience in a Med-tech environment is essential Experience of 6 Sigma quality methods would be a distinct advantage. Materials engineering experience/quality materials testing knowledge is an advantage Experience of leading a team is an advantage. 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. Quality 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 Physical Demands Sitting/standing, free to move around Walking Sustained visual concentration on small areas, such as monitors, screens The job works in generally good conditions with occasional exposure (10% - 33%) to noise, odours, dust, drafts, chemicals, operating machinery, temperature extremes, hazardous substances, etc. Occasional overnight travel is required. Typical Experience 4 years experience in a quality role within Health Tech manufacturing environment Typical Education Bachelor's degree in related field 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 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. To Apply Please forward your CV via the APPLY Now button below.
