92 Manufacturing Process jobs in Ireland

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.

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

Process Improvement Project Engineer Job Purpose: Reporting to the CEO you will be designing, developing, & optimising manufacturing processes to unlock capacity, eliminate bottlenecks, & enhance operational efficiency. You will drive scalable growth while maintaining the highest standards of product quality, safety, & compliance, identifying barriers to growth, recommending improvements, & leading strategic process optimisation initiatives. Key Responsibilities you will: - Process Documentation & Barrier Identification Lead the effort to document barriers to growth & operational inefficiencies within current production lines. Develop detailed process maps & identify areas for improvement, collaborating with cross-functional teams to implement solutions. Recommend future capital investment needs based on identified process constraints & opportunities for growth. Process Design To work closely with the R&D & Engineering teams to design sustainable aligned with future business needs. Lead all other initiatives to grow manuf. capability inc. the design & dev. of new manuf. facilities to support business scalability. Process Optimisation & Capacity Mgt. Conduct in-depth analysis of current production processes to identify capacity constraints, inefficiencies, across all technologies. Develop & implement strategies to resolve capacity issues, improve throughput, reduce batch fails & maximise yields & production output. Work closely with the operations team to optimize resource allocation & production scheduling & reduce downtime Lead initiatives to enhance plant capacity utilisation through process re-engineering & Lean Manufacturing principles. Continuous Improvement Promote & drive the company's continuous improvement programme using Lean/Six Sigma methodologies & principles. Design & implement process improvements that enhance product quality, reduce waste, & optimise yield. Monitor & report on (KPIs) to track the impact of improvements & ensure alignment with company goals Project Mgt. Lead process improvement projects from initiation through to implementation, ensuring projects are completed on time, within budget, & with minimal disruption to production. Develop & manage project timelines, resources, & budgets, ensuring effective execution of process optimisation initiatives. Collaboration & Stakeholder Mgt. Collaborate with operations, engineering, maintenance, S&T & R&D teams to ensure alignment in achieving operational goals & implementing process improvements. Effectively communicate process changes, new methodologies, & best practices effectively to all levels of staff. Work with the Senior Leadership Team to align process improvement strategies with broader business objectives. Training & Development - support the training & dev of operations staff on new processes, equipment, & operational procedures. CapEx - Lead all other initiatives to exp&/unlock manuf. capability inc. the location & design of a new manufacturing facility. Demonstrate financial discipline & compliance to overall Capex policy. Skills & Qualifications / Experience you will bring: - 3-5 years in process Eng or Operations management within manufacturing ideally in the food industry. BSc/BA in a Business project management or engineering related discipline. Exp. with automation tech, digital manufacturing, data-driven process optimisation Strong operational, commercial awareness, sound judgment & decision-making capability. Expertise in process mapping, root cause analysis, & process reengineering. In-depth knowledge of statutory & regulatory requirements of Food Safety, Customer Codes of Practice, H&S, & Env. Compliance. Can implement Lean Manuf. principles & CI methodologies. Strong problem-solving ability for mech & process-related challenges, addressing root causes. Exceptional stakeholder mgt. skills, inc. exp. work with employees, customers, auditors, & vendors/contractors. Proven negotiation & influencing skills in complex operational environments Excellent communication skills (both verbal & written) sharing technical concepts easily . Collating, analysing, & presenting data to support strategic decision-making. Challenge status quo & drive meaningful change in a constructive & professional manner. Strong business acumen with a proactive & strategic mindset. Enthusiastic, energetic, & optimistic with a can-do attitude. Working 4 days on site and 1 from home. The Benefits include: Commensurate salary negotiable Laptop, phone, P-card; Daytime role (M to F) 08:30 - 17:30 and at least four days on site. Skills: project engineering NPI food production process improvement

Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by diversity and inclusion, talented peers, comprehensive benefits and career development opportunities. Come make an impact on the communities we serve as you help us advance health equity on a global scale. Join us to start **Caring. Connecting. Growing together.**
**About the Role**
We are looking for a dynamic, inspiring, and strategic Transformation Leader to steer our organization through a period of significant change and growth. The ideal candidate will be a charismatic individual who not only envisions the future of our organization but also possesses the ability to motivate and lead our team toward that future. We have a key leadership role open for the Director Business Performance & Process Improvement; Payment Integrity based in Ireland.
_Careers with Optum offer flexible work arrangements and individuals who live and work in the Republic of Ireland will have the opportunity to split their monthly work hours between our Dublin and Letterkenny offices and telecommuting from a home-based office._
**Primary Responsibilities:**
Responsible for the identification of process improvements to support affordability savings through:
+ Develop Clinical Business Performance Improvement Strategy across Optum Health value streams to support an ambitious growth target of medical cost savings
+ Lead on implementing continuous improvements or strategic improvements to lead PI portfolio for Optum Health and support Gross Medical Cost Savings of approximately $ 3 Billion
+ Leadership and strategic planning skills to drive strategic operating model of the business keeping in mind the growth/innovation pillars to support the business
+ Develop and articulate Behavioral Health Payment Integrity Business Process Improvement & Transformation Strategy aligning it with our core values and business goals
+ Lead and inspire a culture of innovation, continuous improvement, and adaptability across all levels of the organization to support an ambitious growth target and medical cost savings
+ Strategize & lead Transformation roadmap to achieve multi year benefits in collaboration with Product, Technology, analytics & Automation leaders
+ Drive organizational change initiatives, ensuring they are strategically aligned, effectively communicated, and successfully implemented
+ Create a high performing process exceeding all KPIs, & SLAs in partnership with Operations, Analytics and automation
+ Ensure operational performance improvements are tracked accurately, by establishing and automating statistical control models for value streams, utilizing internal tools and processes
+ Drive changes to performance metrics in partnership with finance, Analytics, workforce management / industrial engineering and ensuring benefits are accounted in P&L accurately
+ Communicate with Leadership/Senior Leadership about progress, challenges and actions required to remove hurdles
+ Provide guidance and assistance to internal and external (client) partners to ensure programs and strategies are implemented effectively and value realized
+ Collaborate with stakeholders, ability to influence without authority to gain support and buy-in for proposed business process solutions and adherence to team requirements
+ Stay up-to-date with industry trends, emerging technologies, and best practices in business transformation
**Required Qualifications**
+ Bachelor's Degree or Undergraduate degree with equivalent experience in Business Operations, Transformation, Change Management and Strategy
+ Demonstrated ability to develop and implement successful organizational change initiatives
+ Exceptional communication and interpersonal abilities, with the skill to inspire and motivate teams
+ A track record of fostering an inclusive and collaborative work environment
+ Prove track record in managing large scale complex programs within a matrix environment
+ Trained in process improvement and change management programs like Six Sigma, Lean or equivalent degree from reputed university
+ Working knowledge of US health care and payment integrity in specific
**Preferred Qualifications**
+ Six Sigma Black Belt certified with in-depth understanding of LEAN process
+ Knowledge / understanding of CPC coding
**Careers with Optum.** Here's the idea. We built an entire organization around one giant objective; make the health system work better for everyone. So when it comes to how we use the world's large accumulation of health-related information, or guide health and lifestyle choices or manage pharmacy benefits for millions, our first goal is to leap beyond the status quo and uncover new ways to serve. Optum, part of the UnitedHealth Group family of businesses, brings together some of the greatest minds and most advanced ideas on where health care has to go in order to reach its fullest potential. For you, that means working on high performance teams against sophisticated challenges that matter. Optum, incredible ideas in one incredible company and a singular opportunity to do your life's best work.SM
_At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone-of every race, gender, sexuality, age, location and income-deserves the opportunity to live their healthiest life. Today, however, there are still far too many barriers to good health which are disproportionately experienced by people of color, historically marginalized groups and those with lower incomes. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes - an enterprise priority reflected in our mission._
_Diversity creates a healthier atmosphere: Optum is an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to gender, civil status, family status, sexual orientation, disability, religion, age, race, and membership of the Traveller community, or any other characteristic protected by law. Optum is a drug-free workplace. © 2024 Optum Services (Ireland) Limited. All rights reserved._

In this Manufacturing Engineering role, you will provide Engineering technical knowledge to resolve production issues and implement changes in a Medical Device Manufacturing Facility to support the sites Continuous Improvement journey. This will include providing technical leadership on cleaning, sealing and packaging Medical devices and working with the team to meet cell efficiency and monthly targets, improve reliability, reduce scrap and validation of new machinery and equipment.
This role will really suit an innovative problem solver with a positive attitude who enjoys a fast paced working environment.
Key Areas of Responsibility
+ Ensure quality of process and product as defined in appropriate OS and Material specifications.
+ Ensure GMPs and system safety.
+ Support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.
+ Provide training for manufacturing team members.
+ Interface with Materials Science, Design and Quality Assurance departments to provide customer with a quality product in a timely manner.
+ Validation, Appraisal and support of machining suppliers and raw material suppliers e.g. packaging components.
+ Communicate and participate in system and process troubleshooting with support team members and with external agents.
+ Lead and participate cross functional and cross divisional process improvement initiatives.
+ Provide engineering support for new Product and new process introduction, ensuring that all activities are completed and documented in accordance with Stryker New product Development Process.
+ Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.
+ Conduct Gauge R&R studies for products and new processes.
+ Carry out structured problem solving.
+ Application and development of statistical tools for use in driving continuous improvement projects.
+ All other duties as assigned.
**Key Requirements**
+ Level 8 Degree in Engineering, Science or related discipline
+ Has 0- 2 years' experience in a manufacturing environment.
+ Business understanding of operations and manufacturing principles.
+ High level of PC Skills required.
+ Flexibility essential.
+ Strong communication skills with both internal and external stakeholders.
+ Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment.
+ The individual should enjoy working in a dynamic and results motivated team environment.
+ Knowledge of FDA requirements.
+ Knowledge of six sigma and Lean Manufacturing
+ Ability to effectively work cross-functionally with Advanced Operations, Quality, etc.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

Purpose of Role:
The Manufacturing Engineer (ME) will provide engineering and process support to ensure successful implementation of 2D barcoding in line with EU MDR requirements.
This role will focus on supporting technical strategy execution, process validation, and operational readiness across both internal manufacturing and supplier sites.
Key Responsibilities:
+ Support technical execution of 2D barcode implementation, including validation activities (VP, IQ, OQ, PQ).
+ Partner with Quality Engineers (QEs) and Supplier Quality Engineers (SQEs) to assess and confirm laser marking equipment compatibility and process qualification at both supplier and internal sites.
+ Assist in First Article Inspection (FAI) preparation, reviewing supplier provided verification data and ensuring compliance to marking requirements.
+ Update and maintain manufacturing documentation (DCP, PFMEA, SOPs) to reflect new barcoding processes.
+ Collaborate with operations teams to ensure inspection readiness (visual inspection, barcode verifier checks).
+ Troubleshoot and provide technical support during initial marking trials and confidence runs.
+ Support scrap management, label obsolescence, and carton switchovers as required for Go-Live phases.
+ Actively contribute to risk assessments, ensuring process robustness and alignment with MDR and GMP requirements.
Required Skills & Experience:
+ 2-4 years' experience in a regulated manufacturing environment (medical device preferred).
+ Exposure to process validation and FAI/PPAP activities in a regulated environment.
+ Familiarity with laser marking or UDI/2D barcoding processes desirable.
+ Strong problem solving and root cause analysis capability (Six Sigma / Lean tools beneficial).
+ Proven ability to work collaboratively with cross functional teams (QE, SQE, and Operations).
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.