480 Jobs in Galway

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
As a Senior Electrical Engineer, you will design, develop, and integrate complex electrical systems for Medtronic's innovative Cardiac Ablation Solutions products. This role provides a unique opportunity to lead challenging projects, mentor team members, and contribute directly to life-changing technologies. You will work cross-functionally with teams in mechanical engineering, software development, quality assurance, and manufacturing to drive projects from concept through production. Your work will help Medtronic achieve its mission of alleviating pain, restoring health, and extending life for millions of patients worldwide.
The Cardiac Ablations Solutions Unit develops life-restoring therapies and healthcare solutions that span the care continuum; integrating technologies and applying clinical and economic evidence to increase patient access, improve efficiency of procedures and deliver successful patient outcomes.
This position is in Galway, Ireland within the Cardiac Ablation Solutions Operating Unit and requires 4 days on-site per week minimum.
We believe that when people from different cultures, genders, and points of view come together, innovation is the result -and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive.
**_Come for a job, stay for a career!_**
**A Day in The Life Of:**
+ Lead or contribute to the design, development, and testing of electrical systems and circuits for medical devices, ensuring compliance with applicable regulatory standards (e.g., IEC 60601).
+ Lead or contribute to technical project planning, establish timelines, define deliverables, and proactively identify and mitigate potential risks.
+ Develop detailed specifications, schematics, and PCB layouts, collaborating closely with cross-functional teams to meet design and performance requirements.
+ Perform system-level integration of hardware, firmware, and software components.
+ Conduct risk assessments and root cause investigations for electrical issues, implementing robust corrective and preventive actions.
+ Manage product changes and related change control activities, ensuring design documentation (e.g., BOMs, specifications, drawings) is updated and maintained accurately.
+ Partner with reliability and manufacturing teams to optimize designs for scalability, cost efficiency, and high performance.
+ Support verification and validation activities to ensure the safety, compliance, and efficacy of the product.
+ Design, develop, and qualify functional and safety test systems at both the product and PCB levels.
+ Investigate and analyze field-returned products, conducting engineering analyses and testing to determine root causes of failures.
+ Support and potentially own CAPA (Corrective and Preventive Actions) processes and manage issue escalations to resolution.
+ Provide troubleshooting and problem-solving support to manufacturing teams and key suppliers, aiming to increase yields, maintain process capabilities, and improve cost-efficiency.
+ Support internal and external regulatory compliance audits, ensuring adherence to quality and safety standards.
+ Mentor and coach junior engineers, fostering a collaborative, innovative, and high-performing engineering environment.
+ Stay current with advancements in electrical engineering, emerging technologies, and industry best practices.
**Key Skills & Experience**
**Must Have - Minimum Requirements:**
+ Bachelor's degree in engineering required with a minimum of 4 years of electrical design experience or advanced degree with a minimum of 2 years electrical design experience
**Preferred Knowledge and Experience:**
+ Experience in medical device or highly regulated industries
+ Experience with analog, digital, high voltage or RF circuit design
+ Solid understanding of EMC design and test principles per IEC 60601
+ Experience with system-level integration of hardware and firmware
+ Hands-on experience with prototyping, testing, and debugging PCB assemblies
+ Experience in developing hardware test systems for design verification or production testing
+ Demonstrated skills in writing engineering documents (specifications, test plans, etc.)
+ Experience with analysis, simulation, and CAD tools for PCB design (e.g., Minitab, MATLAB, SPICE, Altium, Cadence)
+ Knowledge of Design for Manufacturing and Test (DFM & DFT) principles
+ Knowledge of Six Sigma, Lean, or other problem-solving methodologies
+ Strong verbal and written communication skills
+ Team-oriented mindset with a collaborative work ethic
**Medtronic offer a competitive salary and flexible Benefits Package**
**#IJA**
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. **A Day in the Life** **Medtronic** At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations. **Our Purpose** Within our Structural Heart Design Assurance Group in Medtronic, plc, we focus on providing Quality support across all aspects of PDP from pre market product development to post market product surveillance. We participate in the design process to ensure the performance and safety of the Structural Heart devices we develop, is assured and maintained throughout the product lifecycle. _Come for a job, stay for a career!_ **A Day** **i** **n** **The Life** **Of:** + You will serve as extended team member on a PDP Project representing the Design Assurance function and will report dotted line to the quality lead on the project. + You will lead strategies for risk management, test method validations, design verification and shelf-life protocols / reports. + You will be responsible for keeping abreast of industry best practice with respect to product design. + You will maintain expert, up to date knowledge of developments in regulatory compliance requirements for product design, development, transfer and commercialisation activities.  + You will be required to liaise with departments, both internally and externally to build strong collaborative partnerships. + You will be required to provide Quality input into new product development, process improvements and change control. + As required, you will support cross functional teams to design protocols to ensure that new products/ product changes are adequately evaluated/tested with respect to standard requirements. + Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance. **Key Skills & Experience** + Requires advanced knowledge of job area combining breadth and depth, typically obtained through advanced education combined with experience. + Requires a minimum Level 8 degree in Engineering or other relevant discipline with minimum 4 years' relevant experience. + Experience in a highly regulated industry, preferably medical devices. + You are a dynamic team player and leader and can work effectively and proactively on cross-functional teams. + You are experienced to a competent level within Medical Device product design. + Initiates and Leads Change, Collaborates and Creates Alignment, Drives Accountability and Thinks Critically and Makes Sound Decisions are a must. + Excellent communication and ability to influence is critical to the role. + Flexibility to travel <10% of time desirable. **Medtronic offer a competitive** **s** **alary and flexible Benefits Package** #IJ **Physical Job Requirements** The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.  **Benefits & Compensation** **Medtronic offers a competitive Salary and flexible Benefits Package** A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). **About Medtronic** We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people. We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity here ( We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people. We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. **We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives. **We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough. **This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will. + **Build** a better future, amplifying your impact on the causes that matter to you and the world + **Grow** a career reflective of your passion and abilities + **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning These commitments set our team apart from the rest: **Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need. **Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms. **Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls. **Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities. For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support. This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( . For updates on job applications, please go to the candidate login page and sign in to check your application status. If you need assistance completing your application please email To request removal of your personal information from our systems please email

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
**Medtronic**
At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress and deliver meaningful innovations.
**Our Purpose**
At our Quality Department in Medtronic, plc, we focus on supporting the product value stream to ensure that customer and patient needs are met every day. Our key focus is on delivering and maintaining a high level of Quality to ensure that business and performance goals are achieved. The Senior Quality Engineer role is critical in supporting key department metrics by contributing to the global strategy and to deliver on our mission to contribute to human welfare by supporting the manufacture of products that alleviate pain, restore health, and extend life. In our Structural Heart Post-Market Quality Department, we focus on partnering with internal and external colleagues to plan and execute Post-Market strategies for continuous improvement of products, methodologies, processes, and departmental interfaces, while working within the organisation to build, motivate and lead high performance teams.
**_Come for a job, stay for a career!_**
**A Day in the life of:**
Responsibilities may include the following and other duties may be assigned.
+ Apply knowledge of design control principles and quality engineering techniques throughout the product development process and the product lifecycle.
+ Lead and manage the receive inspection function ensuring incoming materials and components meet defined specifications and regulatory requirements.
+ Lead root cause analysis and resolution of non-conformances related to incoming material.
+ Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
+ Provide input to design and manufacturing deliverables including material specifications, drawings, inspection procedures to ensure that the resulting products can be adequately manufactured and tested.
+ Understand risk management concepts used throughout the quality system to successfully meet FDA, ANSI/AAMI/ISO 14971:2019, and ANSI/AAMI/ISO 13485:2016 requirements.
+ Lead cross-functional teams including issue triages for CAPAs or Hazard Analysis, etc.
+ As necessary, proposes changes in design or formulation to improve system and/or process reliability.
+ Supporting internal and external audits (MDR/MDSAP/FDA etc).
**Key Skills & Experience**
+ Requires advanced knowledge of job area combining breadth and depth, typically obtained through advanced education combined with experience.
+ Requires a minimum Level 8 degree in Engineering or other relevant discipline with minimum 4 years' relevant experience or advanced degree with minimum 2 years of relevant experience.
+ Must have practical knowledge of project management.
+ Experience in a highly regulated industry, preferably medical devices.
+ Experience with solving complex issues by interacting with cross functional groups.
+ Proven ability to operate in a matrix organisation and navigate complex business systems, regulations, standards, and performance requirements.
+ Knowledge of reliability tools and practices that effectively support requirements, design, integration and verification, and validation.
+ Demonstrated critical thinking skills with focus on improved system performance outcomes and positive business impact.
+ Excellent communication and ability to influence is critical to the role.
+ Ability to work independently to plan and schedule own activities necessary to meet timelines.
**Medtronic offer a competitive salary and flexible Benefits Package**
**#IJA**
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
responsible for full cycle recruitment for the Ireland Manufacturing and R&D facilities
In our Talent Acquisition Centre of Expertise (CoE) in Medtronic, plc, we focus on sourcing and securing skilled talent for our operations sites in Ireland. As a Talent Acquisition Specialist, you partner directly with hiring managers to support selection and recruitment of professionals across the different departments and sites in Ireland.
**Responsibilities may include the following and other duties may be assigned:**
+ Lead full recruitment cycle activities for Ireland Manufacturing
+ Support strategic talent acquisition projects, processes, and programs to meet business needs
+ Design and implement sourcing strategies to identify, engage, and build lasting relationships with prospective candidates
+ Manage the applicant tracking system (Workday Recruit) effectively and accurately
+ Partner with Hiring Managers to create competitive and attractive offers to secure top talent
+ Ensure an excellent candidate experience by maintaining clear and regular communication with both candidates and hiring managers
+ Contribute as a team player with a growth mindset, sharing expertise and learning from colleagues across the team and wider organization
+ Build and maintain strong, professional, and trusting relationships with business partners
**Required Knowledge and Experience:**
+ Proven experience as a Talent Acquisition Specialist, Recruiter, or in a similar HR role
+ Solid understanding of full-cycle recruiting, including sourcing, screening, interviewing, and onboarding
+ Experience with Applicant Tracking Systems (ATS), preferably Workday
+ Excellent communication and interpersonal skills, with the ability to build strong relationships with candidates and hiring managers
+ Ability to manage multiple requisitions and priorities in a fast-paced environment
#IJA #IJ
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email

Req ID:
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 oportunity 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 SOP's, Control Plans, and performing validation (FAT, SAT, IQ, OQ, PQ).
+ Demonstrated ability to effectively communicate manufacturing plans, proposals, and results, and negotiate options at executive management levels.
+ Experience in analytical and problem-solving skills.
+ Excellent interpersonal and communication skills.
+ A strong aptitude for report writing and data analytics.
+ An advantage with knowledge of the medical device industry and of 21 CFR, (820, 11), ISO13485, specifically in the areas of Change Control and Validation.
What are we looking for?
+ A minimum of 4+ years' experience in a Process Engineering role, with a proven track record of involvement in projects and teams.
+ A Primary Degree in an Engineering/Science discipline.
+ Medical Device AND/OR Automation experience an advantage.
+ Experience in a highly automated manufacturing environment.
+ An ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically, and make sound decisions.
**What do we ofer?**
+ 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.

01 - Student IL 1
Req ID:
Remote Position: No
Hiring Manager: Ray O'Hara
Band: 01
Region: Europe
Country: Ireland
State/Province: Galway
City: Galway
**General Overview**
**Functional Area:** * FLX - Flex Staff
**Career Stream:** FLEX STAFF
**Role:** FLEX STAFF
**SAP Short Name:** STU
**Job Title:** Student IL
**Job Code:** STU-FLX-IL
**Job Level:** Band 01
**Profile-Holding:** N
**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.
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.

Req ID:
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**
Join Celestica Galway as a Shift Engineer! C Shift: Thursday, Friday, Saturday 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 SOP's, Control Plans, and performing validation (FAT, SAT, IQ, OQ, PQ).
+ Demonstrated ability to effectively communicate manufacturing plans, proposals, and results, and negotiate options at executive management levels.
+ Experience in analytical and problem-solving skills.
+ Excellent interpersonal and communication skills.
+ A strong aptitude for report writing and data analytics.
+ An advantage with knowledge of the medical device industry and of 21 CFR, (820, 11), ISO13485, specifically in the areas of Change Control and Validation.
What are we looking for?
+ A minimum of 4+ years' experience in a Process Engineering role, with a proven track record of involvement in projects and teams.
+ A Primary Degree in an Engineering/Science discipline.
+ Medical Device AND/OR Automation experience an advantage.
+ Experience in a highly automated manufacturing environment.
+ An ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically, and make sound decisions.
**What do we ofer?**
+ 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.

Req ID:
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**
Join us as Shift Engineer: B Shift: Sunday, Monday, Tuesday and every second Saturday night: 8 PM - 8 AM
Your day-to-day activities will include the following.
+ Create, execute, coordinate, and support the design of experiments, test methods, protocols, specifications, and validation documentation (IQ/OQ/PQ) and oversee the development and execution of qualification trials/characterization studies.
+ Oversee and analyze the performance of equipment, vision systems and machines, optimizing process parameters to eliminate non-conforming products, low yields, or product quality issues.
+ Champion and drive continuous improvement processes for production areas using structured Process Capability and Lean Six Sigma methodologies, leading cross-functional teams in these initiatives.
+ Manage multiple projects, generate comprehensive project plans, and support as a team player project teams to drive completion and success, ensuring alignment with strategic objectives.
+ Support the maintenance and calibration of critical equipment-systems, ensuring compliance and optimizing maintenance schedules.
+ Work with cross-functional teams and external vendors to integrate new products, processes, and technologies into the existing manufacturing area, leading the technology transfer and implementation.
**Detailed Description**
Performs tasks such as, but not limited to, the following:
+ Design, develop, and implement new manufacturing processes to support customer products.
+ Develop application software and tooling for a series of complex machines and mechanical process steps within a manufacturing sector.
+ Execute with support, capability of machines and process steps using Design of Experiments and statistical methods to ensure maximum utilization of critical resources, maximum throughput, minimum cost and capacity growth; involves integrating equipment, people, material flow, and information systems.
+ Solve technical product, process, component, and related problems that affect the efficient operation and/or manufacture of products.
+ Provide feedback to product designers on suitability of designs for manufacturability with supervision.
**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 SOP's, Control Plans, and performing validation (FAT, SAT, IQ, OQ, PQ).
+ Demonstrated ability to effectively communicate manufacturing plans, proposals, and results, and negotiate options at executive management levels.
+ Experience in analytical and problem-solving skills.
+ Excellent interpersonal and communication skills.
+ A strong aptitude for report writing and data analytics.
+ An advantage with knowledge of the medical device industry and of 21 CFR, (820, 11), ISO13485, specifically in the areas of Change Control and Validation.
What are we looking for?
+ A minimum of 4+ years' experience in a Process Engineering role, with a proven track record of involvement in projects and teams.
+ A Primary Degree in an Engineering/Science discipline.
+ Medical Device AND/OR Automation experience an advantage.
+ Experience in a highly automated manufacturing environment.
+ An ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically, and make sound decisions.
**What do we ofer?**
+ 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.

Req ID:
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! D Shift: Wednesday, Thursday, Friday and every second Saturday night: 8 PM - 8 AM
Your day-to-day activities will include the following.
+ Create, execute, coordinate, and support the design of experiments, test methods, protocols, specifications, and validation documentation (IQ/OQ/PQ) and oversee the development and execution of qualification trials/characterization studies.
+ Oversee and analyze the performance of equipment, vision systems and machines, optimizing process parameters to eliminate non-conforming products, low yields, or product quality issues.
+ Champion and drive continuous improvement processes for production areas using structured Process Capability and Lean Six Sigma methodologies, leading cross-functional teams in these initiatives.
+ Manage multiple projects, generate comprehensive project plans, and support as a team player project teams to drive completion and success, ensuring alignment with strategic objectives.
+ Support the maintenance and calibration of critical equipment-systems, ensuring compliance and optimizing maintenance schedules.
+ Work with cross-functional teams and external vendors to integrate new products, processes, and technologies into the existing manufacturing area, leading the technology transfer and implementation.
**Detailed Description**
Performs tasks such as, but not limited to, the following:
+ Design, develop, and implement new manufacturing processes to support customer products.
+ Develop application software and tooling for a series of complex machines and mechanical process steps within a manufacturing sector.
+ Execute with support, capability of machines and process steps using Design of Experiments and statistical methods to ensure maximum utilization of critical resources, maximum throughput, minimum cost and capacity growth; involves integrating equipment, people, material flow, and information systems.
+ Solve technical product, process, component, and related problems that affect the efficient operation and/or manufacture of products.
+ Provide feedback to product designers on suitability of designs for manufacturability with supervision.
**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 SOP's, Control Plans, and performing validation (FAT, SAT, IQ, OQ, PQ).
+ Demonstrated ability to effectively communicate manufacturing plans, proposals, and results, and negotiate options at executive management levels.
+ Experience in analytical and problem-solving skills.
+ Excellent interpersonal and communication skills.
+ A strong aptitude for report writing and data analytics.
+ An advantage with knowledge of the medical device industry and of 21 CFR, (820, 11), ISO13485, specifically in the areas of Change Control and Validation.
What are we looking for?
+ A minimum of 4+ years' experience in a Process Engineering role, with a proven track record of involvement in projects and teams.
+ A Primary Degree in an Engineering/Science discipline.
+ Medical Device AND/OR Automation experience an advantage.
+ Experience in a highly automated manufacturing environment.
+ An ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically, and make sound decisions.
**What do we ofer?**
+ 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.