63 Process Engineering jobs in Ireland

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Engineering Automation position is a unique career opportunity that could be your next step towards an exciting future.
The Director of Engineering will develop and drive Process Automation in providing technical expertise in the design, prototyping, assembly, development, and troubleshooting of innovative automation system in partnership with R&D and NPD groups. Continuing to innovate and improve by extracting more opportunities and benefit from automation technology.
**How you'll make an impact:**
+ Initiate and lead the design, prototyping, assembly, development, and troubleshooting of highly complex automation systems in support of R&D, New Product Development / Introduction, instilling DFM.Lead in identifying risk, developing mitigation strategies, alternative solutions, resolving issues, etc. in collaboration with cross functional groups and key stakeholders.Oversee, inspire, and develop SMEs, and retain a technical talent to ensure automation knowledge continuity and knowledge transfer capabilities from Singapore site to the global. Develop a robust talent development plan in alignment with functional growth strategies of the department.
+ Manage resource planning, project planning, budgeting, expense priorities, performance management, and working through team managers to achieve results.
+ Identify opportunities for and drive the development and management of multiple, highly complex automated systems that resolve manufacturing and/or product inspection challenges.
+ Provide insight to stakeholders on current automation capabilities to ensure they are reusable in broader initiatives while developing new capabilities
+ Build strong relationships with stakeholders, ensuring collaboration, professionalism and cooperation against scope, timelines and budget for strategic automation program activities.
+ Embrace Agile Methodology and working efficiently with ambiguity.
+ Responsible for the tactical execution of value stream mindset and culture of continuous improvement based on Edwards Production System (EPS)
**What you'll need to have (Required):**
+ Minimum Bachelors degree in Engineering or related
+ Experience in Automation deployment
+ Track record in management of technical and/or automation disciplines and/or agile methodology
+ Experience working in a regulated industry
**What else we look for (Preferred):**
+ Proven successful project management leadership skills
+ Proficient in both Microsoft Office Suite and Solidworks
+ Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making
+ Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
+ Determines or effectively recommends course of action after considering potential risks of alternatives
+ Ability to read and interpret drawings per ASME Y14.5
+ Ability to translate technical information to all levels of the organizations
+ Experience in PLC logic and programming, and integration of sensors, sub-systems, and controllers Preferred
+ Experience in development, integration, and programming of Vision Systems Preferred
+ Extensive knowledge and understanding of principles, theories, and concepts relevant to controls engineering
+ Demonstrated ability to work with teams to complete critical milestones under pressure with short deadlines
+ Expert knowledge and understanding of mechanical design & machine building practices
+ Expert understanding of fixture development & system integration
+ Expert understanding of materials and manufacturing processes
+ Extensive understanding of Six Sigma concepts with proven ability to apply to projects
+ Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Engineering Automation position is a unique career opportunity that could be your next step towards an exciting future. The Director of Engineering will develop and drive Process Automation in providing technical expertise in the design, prototyping, assembly, development, and troubleshooting of innovative automation system in partnership with R&D and NPD groups. Continuing to innovate and improve by extracting more opportunities and benefit from automation technology. How you'll make an impact: Initiate and lead the design, prototyping, assembly, development, and troubleshooting of highly complex automation systems in support of R&D, New Product Development / Introduction, instilling DFM. Lead in identifying risk, developing mitigation strategies, alternative solutions, resolving issues, etc. in collaboration with cross functional groups and key stakeholders. Oversee, inspire, and develop SMEs, and retain a technical talent to ensure automation knowledge continuity and knowledge transfer capabilities from Singapore site to the global. Develop a robust talent development plan in alignment with functional growth strategies of the department. Manage resource planning, project planning, budgeting, expense priorities, performance management, and working through team managers to achieve results. Identify opportunities for and drive the development and management of multiple, highly complex automated systems that resolve manufacturing and/or product inspection challenges. Provide insight to stakeholders on current automation capabilities to ensure they are reusable in broader initiatives while developing new capabilities Build strong relationships with stakeholders, ensuring collaboration, professionalism and cooperation against scope, timelines and budget for strategic automation program activities. Embrace Agile Methodology and working efficiently with ambiguity. Responsible for the tactical execution of value stream mindset and culture of continuous improvement based on Edwards Production System (EPS) What you'll need to have (Required): Minimum Bachelors degree in Engineering or related Experience in Automation deployment Track record in management of technical and/or automation disciplines and/or agile methodology Experience working in a regulated industry What else we look for (Preferred): Proven successful project management leadership skills Proficient in both Microsoft Office Suite and Solidworks Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives Determines or effectively recommends course of action after considering potential risks of alternatives Ability to read and interpret drawings per ASME Y14.5 Ability to translate technical information to all levels of the organizations Experience in PLC logic and programming, and integration of sensors, sub-systems, and controllers Preferred Experience in development, integration, and programming of Vision Systems Preferred Extensive knowledge and understanding of principles, theories, and concepts relevant to controls engineering Demonstrated ability to work with teams to complete critical milestones under pressure with short deadlines Expert knowledge and understanding of mechanical design & machine building practices Expert understanding of fixture development & system integration Expert understanding of materials and manufacturing processes Extensive understanding of Six Sigma concepts with proven ability to apply to projects Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process click the Continue to Application or Login/Register to apply button below.

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Engineering Automation position is a unique career opportunity that could be your next step towards an exciting future.
The Senior Manager will develop Process automation in providing technical expertise in the design, prototyping, assembly, development, and troubleshooting of innovative automation system in partnership with R&D and NPD groups. Continuing to innovate and improve by extracting more opportunities and benefit from automation technology.
**How you'll make an impact:**
+ Lead the design, prototyping, assembly, development, and troubleshooting of highly complex automation systems in support of New Product Development / Introduction, instilling DFM.Lead in identifying risk, developing mitigation strategies, alternative solutions, resolving issues, etc. in collaboration with cross functional groups and key stakeholders.
+ Lead and develop SME's and retain a technical talent to ensure automation knowledge continuity and knowledge transfer capabilities from the Ireland site to Delivery System Network. Develop a robust talent development plan in alignment with functional growth strategies of the department.
+ Manage resource planning, project planning, budgeting, expense priorities, performance management, and working through team managers to achieve results.
+ Identify opportunities for and drive the development and management of multiple, highly complex automated systems that resolve manufacturing and/or product inspection challenges.
+ Provide insight to stakeholders on current automation capabilities to ensure they are reusable in broader initiatives while developing new capabilities.
+ Write and submit successful proposals for automation and digital grant funding to external agencies.
**What you will need to have (Required):**
+ Minimum Bachelors degree in Engineering or related
+ Experience in Automation deployment
+ Track record in management of technical and/or automation disciplines and/or agile methodology
+ Experience working in a regulated industry
**What else we look for (Preferred):**
+ Proven successful project management leadership skills
+ Proficient in both Microsoft Office Suite and Solidworks
+ Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making
+ Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
+ Determines or effectively recommends course of action after considering potential risks of alternatives
+ Ability to read and interpret technical drawings
+ Ability to translate technical information to all levels of the organizations
+ Experience in PLC logic and programming, and integration of sensors, sub-systems, and controllers Preferred
+ Experience in development, integration, and programming of Vision Systems Preferred
+ Extensive knowledge and understanding of principles, theories, and concepts relevant to controls engineering
+ Demonstrated ability to work with teams to complete critical milestones under pressure with short deadlines
+ Expert level of knowledge and understanding of mechanical design & machine building practices
+ High level of understanding of fixture development & system integration
+ High level of understanding of materials and manufacturing processes
+ Extensive understanding of Six Sigma concepts with proven ability to apply to projects
+ Adhere to all company rules and requirements (e.g., Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Engineering Automation position is a unique career opportunity that could be your next step towards an exciting future. The Senior Manager will develop Process automation in providing technical expertise in the design, prototyping, assembly, development, and troubleshooting of innovative automation system in partnership with R&D and NPD groups. Continuing to innovate and improve by extracting more opportunities and benefit from automation technology. How you'll make an impact: L ead the design, prototyping, assembly, development, and troubleshooting of highly complex automation systems in support of New Product Development / Introduction, instilling DFM. Lead in identifying risk, developing mitigation strategies, alternative solutions, resolving issues, etc. in collaboration with cross functional groups and key stakeholders. Lead and develop SME ' s and retain a technical talent to ensure automation knowledge continuity and knowledge transfer capabilities from the Ireland site to Delivery System Network . Develop a robust talent development plan in alignment with functional growth strategies of the department. Manage resource planning, project planning, budgeting, expense priorities, performance management, and working through team managers to achieve results. Identify opportunities for and drive the development and management of multiple, highly complex automated systems that resolve manufacturing and/or product inspection challenges. Provide insight to stakeholders on current automation capabilities to ensure they are reusable in broader initiatives while developing new capabilities. Write and submit successful proposals for automation and digital grant funding to external agencies. What you will need to have (Required): Minimum Bachelors degree in Engineering or related Experience in Automation deployment Track record in management of technical and/or automation disciplines and/or agile methodology Experience working in a regulated industry What else we look for (Preferred): Proven successful project management leadership skills Proficient in both Microsoft Office Suite and Solidworks Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives Determines or effectively recommends course of action after considering potential risks of alternatives Ability to read and interpret technical drawings Ability to translate technical information to all levels of the organizations Experience in PLC logic and programming, and integration of sensors, sub-systems, and controllers Preferred Experience in development, integration, and programming of Vision Systems Preferred Extensive knowledge and understanding of principles, theories, and concepts relevant to controls engineering Demonstrated ability to work with teams to complete critical milestones under pressure with short deadlines Expert level of knowledge and understanding of mechanical design & machine building practices High level of understanding of fixture development & system integration High level of understanding of materials and manufacturing processes Extensive understanding of Six Sigma concepts with proven ability to apply to projects Adhere to all company rules and requirements (e.g., Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process click the Continue to Application or Login/Register to apply button below.

**About Abbott**
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Abbott in Ireland**
Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo.
**Abbott Ireland Diabetes Care Division Donegal**
The Abbott Diabetes Care division based in Donegal Town manufactures FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre system.
**Key Responsibilities**
- Plans and conducts small- to medium-sized assigned projects within engineering specialty requiring conventional types of plans, investigations, and/or equipment validations.
- Maintains a good understanding of customer, business, and technical considerations, incorporating into work/project scoping and planning.
- Coordinates, monitors and manages activity/project implementation, adjusting as required to ensure quality and alignment to plan.
- Estimates and coordinates resources needed (materials, budget, time and people) to accomplish assigned tasks, incorporating contingencies
- Participates in basic economic analysis and feasibility studies related to project alternatives with support.
- Benchmarks and monitors external and internal environments, evaluating changes as potential indicators of future problems and/or opportunities, and preparing for those potential scenarios
- Independently executes the design of products/processes/equipment /systems/facilities using standard engineering theories, concepts, and techniques within the discipline.
- Independently investigates, conducts tests or experiments, gathers data, and performs preliminary analysis, reports findings and communicates recommendations to a variety of stakeholder audiences.
- Creates/modifies designs for intermediate problems, including designing and modifying more complex components/processes, and writing detailed design specifications.
- Reviews and analyzes data for patterns/trends, seeing relationships of growing complexity among the data, drawing insights and making recommendations to pursue opportunities and/or solve problems.
- Conducts root cause analysis to resolve underlying problems, applying a customer-centric lens to identify needs and propose solutions/alterations to meet those needs.
- Implements improvements to methods, designs and processes, proactively sharing and adopting ideas and best practices to reduce cost and optimize efficiencies/effectiveness
- Communicates to a variety of stakeholders using formal and informal media, based on the needs and priorities of the audience
- Builds open, honest, collaborative with a network of colleagues, contractors and vendors by developing an understanding of others' needs, promoting common goals, and following through on commitments.
- Mentors others by sharing technical expertise and providing feedback and guidance within the team and to cross-functional partners
**Minimum Experience Required**
Experience in GMP regulated environment
**Minimum Education Required**
A Bachelors Degree in Engineering, science or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 2+ years of significant engineering and/or operational experience. Additional post-graduate education may contribute towards the desired years of experience.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

Job Description
**Have you ever wanted to make a difference?**
At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional products and branded generic medicines. Our 113,000 colleagues have a daily impact on the life of people in more than 160 countries.
**Abbott Ireland**
In Ireland, Abbott employs over 5,000 people across nine sites. We currently have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**Diabetes Care Kilkenny**
Our new manufacturing facility in Kilkenny, opening in 2024, reflects the growing demand for Abbott's global Diabetes Care products. The facility will be a centre for world-class engineering, quality, medical device manufacturing, and other science-based professionals to produce life-changing technologies, including the FreeStyle Libre 3, a system that automatically delivers real-time, up-to-the-minute glucose readings, with the smallest and thinnest wearable glucose sensor that provides unsurpassed 14-day accuracy and optional glucose alarms directly to smartphones. This enables people with diabetes to live the best and fullest lives they can.
At Abbott in Kilkenny, you can shape your career as you help shape the future of healthcare.
**This is how you can make a difference at Abbott:**
In this role you will be in charge to apply subject matter knowledge in the area of Pharmaceutical/Biological Process. You will require capacity to apply skills/knowledge within the context of specific needs or requirements.
It will be a very big plus if you can bring experience in developing projects or sites from square one.
As Process Engineer, you will be responsible to:
+ Implement and maintain pharmaceutical/biological processes.
+ Calculate and organize all data for complex process flow sheets including instrumentation and control considerations.
+ Model processes and units operations.
+ Ensure proper sequence of operation and prepares specifications and operating instructions for processing equipment.
+ Conduct tests and measurements throughout stages of production to determine control over such variables as temperature, density, pressure and viscosity.
+ Service, troubleshoot and solve engineering problems with processes or equipment already in operation.
+ Ensure processes and procedures are in compliance with regulations.
+ May be responsible for corrective and preventive actions and investigation management.
**QUALIFICATIONS AND EXPERIENCE**
+ A relevant third level qualification in Engineering/Manufacturing/Science.
+ Minimum 2 years experience in the Engineering/Manufacturing/ Scientific field.
Connect with us at or on LinkedIn at on Facebook at and on Twitter @AbbottNews.
Abbott is an equal opportunities employer.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

Req ID: 126865
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 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: 126865 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: 128120
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 Device AND/OR Automation experience preferred
+ Experience in ISO13485 medical device manufacturing environment is desirable.
+ Relevant project management experience and associated qualifications with NPI experience
+ Someone with an ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically and make sound decisions
+ Someone that is open to the opportunity of short term travel assignments particularly at the early stages of the project.
+ Someone that has excellent customer Management skills and a knowledge of customer and regulatory requirements.
+ Someone that has previous experience of coaching and mentoring junior engineers.
Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).
At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.
COMPANY OVERVIEW:
Celestica (NYSE, TSX: CLS) enables the world's best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development - from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud.
Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers.
Celestica would like to thank all applicants, however, only qualified applicants will be contacted.
Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.