8 Manufacturing Team Lead jobs in Ireland

ADC Biologics Manufacturing Team Lead Function : Operations JobType: Full Time JobID: R Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit our website. Job Description If you want to be a difference maker our people are waiting. See the difference you can make at AbbVie. Working at AbbVie is more than a job. Its a career with meaning. A chance to make a difference, in the world and in your life. We make sure you have everything you need to reach higher ground in your career. From growing and learning together to fostering a supportive space for you to thriveat AbbVie and beyond. Join our dynamic team at AbbVie Ballytivnan (Sligo) and be part of groundbreaking work in Antibody Drug Conjugation (ADC). As a Team Lead in our Biologics division you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, and build an inclusive culture of high performance for the team. Lead and manage the operations team, ensuring adherence to safety, regulatory, and operational requirements. Foster a high-performance culture focused on customer service, quality, compliance, financial performance, and inclusion. Oversee and execute filling, lyophilization, equipment preparation, formulation, buffer preparation, and support processing activities. Prioritize safety and compliance in all activities, conducting regular safety Gembas and promoting a culture of zero safety incidents. Review daily work activities to identify and address high-risk activities. Ensure compliance with EHS standards, procedures, and policies. Promote a culture of contamination control and adherence to aseptic best practices. Effectively deploy and manage team members to meet production schedules. Provide daily reporting on the status of operations and support activities. Lead, motivate, and direct the manufacturing team to maximize effectiveness. Foster team engagement through regular one-on-ones, clear expectations, feedback, performance reviews, and action plans. Develop direct reports through training, challenging tasks, and performance reviews. Promote a culture of Right First Time execution, Behavioral Based Safety, Always Audit Ready, and Human Error Reduction. Drive operational excellence and achieve key operations targets, including OEE. Ensure compliance with safety, environmental, and quality-related SOPs. Collaborate with other Technical Shift Leaders for interdepartmental planning and execution. Schedule human and material resources to meet production schedules. Utilize management infrastructure tools, trackers, visual management, tier meetings, and Gemba walks. Ensure smooth shift handover and communication of performance metrics. Identify and supervise critical process steps during your shift. Achieve financial targets by improving overhead spend, material usage, and labor efficiency. Manage cycle time and identify improvement opportunities. Collaborate with program management, supply chain, technical operations, quality, and engineering for effective planning, scheduling, and execution. Provide technical guidance and approval for manufacturing batch records. Verify and update manufacturing control system transactions accurately and timely. Serve as the key technical contact for aseptic fill-finish activities. Support the documentation and investigation of NCRs. Interface with QA department for interactions with HPRA, FDA, and other health authorities. Lead cross-functional risk assessments and continuous improvement projects. Compile and analyze data to track process performance. Provide technical expertise for investigations, root cause analysis, CAPAs, process improvements, and change control reviews and approvals. Manage compliance issues that may arise during shifts and ensure adherence to regulatory requirements. Qualifications Degree, Masters or PhD in Life Sciences, Process Engineering, Biopharmaceutical Engineering or Chemical Engineering discipline A minimum of 5 years experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry. Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role. Comprehensive understanding of the principles of contamination control and regulatory expectations for aseptic processing. Has a technical background in pharmaceutical, biologics, or similar industries Experience of start-ups and/or new product introductions to bio-pharmaceutical/pharmaceutical facilities (Biologics Preferred). Must be able to lead & project manage these activities. Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality and safety requirements. A minimum of 1 year team direct supervisory experience in a team environment Possesses a strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors. Exercises judgment and advises management as to the appropriate actions. Additional Information Youre here to make a difference. We have the science to turn you into difference makers. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community? Equal Opportunity Employer/Veterans/Disabled.

ADC Biologics Manufacturing Team Lead Function : Operations Job Type: Full Time Job ID: R Company Description Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.

We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio.

For more information about Abb Vie, please visit us at.

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Job Description If you want to be a difference maker our people are waiting.

See the difference you can make at Abb Vie.

Working at Abb Vie is more than a job.

Its a career with meaning.

A chance to make a difference, in the world and in your life.

We make sure you have everything you need to reach higher ground in your career.

From growing and learning together to fostering a supportive space for you to thriveat Abb Vie and beyond.

Join our dynamic team at Abb Vie Ballytivnan (Sligo) and be part of groundbreaking work in Antibody Drug Conjugation (ADC).

As a Team Lead in our Biologics division you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, and build an inclusive culture of high performance for the team.

Lead and manage the operations team, ensuring adherence to safety, regulatory, and operational requirements.

Foster a high-performance culture focused on customer service, quality, compliance, financial performance, and inclusion.

Oversee and execute filling, lyophilization, equipment preparation, formulation, buffer preparation, and support processing activities.

Prioritize safety and compliance in all activities, conducting regular safety Gembas and promoting a culture of zero safety incidents.

Review daily work activities to identify and address high-risk activities.

Ensure compliance with EHS standards, procedures, and policies.

Promote a culture of contamination control and adherence to aseptic best practices.

Effectively deploy and manage team members to meet production schedules.

Provide daily reporting on the status of operations and support activities.

Lead, motivate, and direct the manufacturing team to maximize effectiveness.

Foster team engagement through regular one-on-ones, clear expectations, feedback, performance reviews, and action plans.

Develop direct reports through training, challenging tasks, and performance reviews.

Promote a culture of Right First Time execution, Behavioral Based Safety, Always Audit Ready, and Human Error Reduction.

Drive operational excellence and achieve key operations targets, including OEE.

Ensure compliance with safety, environmental, and quality-related SOPs.

Collaborate with other Technical Shift Leaders for interdepartmental planning and execution.

Schedule human and material resources to meet production schedules.

Utilize management infrastructure tools, trackers, visual management, tier meetings, and Gemba walks.

Ensure smooth shift handover and communication of performance metrics.

Identify and supervise critical process steps during your shift.

Achieve financial targets by improving overhead spend, material usage, and labor efficiency.

Manage cycle time and identify improvement opportunities.

Collaborate with program management, supply chain, technical operations, quality, and engineering for effective planning, scheduling, and execution.

Provide technical guidance and approval for manufacturing batch records.

Verify and update manufacturing control system transactions accurately and timely.

Serve as the key technical contact for aseptic fill-finish activities.

Support the documentation and investigation of NCRs.

Interface with QA department for interactions with HPRA, FDA, and other health authorities.

Lead cross-functional risk assessments and continuous improvement projects.

Compile and analyze data to track process performance.

Provide technical expertise for investigations, root cause analysis, CAPAs, process improvements, and change control reviews and approvals.

Manage compliance issues that may arise during shifts and ensure adherence to regulatory requirements.

Qualifications Degree, Masters or Ph D in Life Sciences, Process Engineering, Biopharmaceutical Engineering or Chemical Engineering discipline A minimum of 5 years experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry.

Detailed knowledge of c GMP and regulatory requirements relating to the pharmaceutical industry is required for this role.

Comprehensive understanding of the principles of contamination control and regulatory expectations for aseptic processing.

Has a technical background in pharmaceutical, biologics, or similar industries Experience of start-ups and/or new product introductions to bio-pharmaceutical/pharmaceutical facilities (Biologics Preferred).

Must be able to lead & project manage these activities.

Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality and safety requirements.

A minimum of 1 year team direct supervisory experience in a team environment Possesses a strong technical knowledge and application of concepts, practices, and procedures.

Works on problems of complex scope where analysis of situations or data involves multiple competing factors.

Exercises judgment and advises management as to the appropriate actions.

Additional Information Youre here to make a difference.

We have the science to turn you into difference makers.

Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community? Equal Opportunity Employer/Veterans/Disabled.

**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.
**Primary Function:**
You are process and system driven and a proven ability to communicate effectively across multiple levels of the organisation. You can assess corrective maintenance and work with engineers and technicians to determine the right actions, spares and people to correct problems. You have a methodical approach and work closely with schedulers to ensure work can be planned and scheduled effectively, with a right first time approach. You have experience working in a regulated environment.
**Main Responsibilities:**
+ Work with Maximo system administrator to develop and manage KPIs and metrics relating to engineering services (and production as required). Plan corrective and preventive maintenance activities by task and priority level:
+ Ensure all EHS/Quality and reliability aspects are considered.
+ Ensure appropriate parts and tools are available.
+ Prepare all permits as required to maintenance activity.
+ Consult with technicians where necessary on corrective work required following PMs or equipment outage.
+ Coordinate with scheduler to ensure PMs and DMs are completed in timely fashion. Manage spare parts and alignment between the maintenance department and stock room. Manage work orders, documentation, and assets within the computerized maintenance management system (CMMS). Engage with contractors as required and ensure all reports, job cards, etc are completed fully in Maximo. Other related tasks as necessary.
+ Manage spares budget to ensure spares budget is adhered too. This includes forecasting and monitoring spend at LBE cycles and on a month-to-month basis.
+ Lead CFT's within Engineering and Operations to annually review reorder points to ensure the correct stock levels are adhered too.
+ Lead the introduction of new process improvement projects ensuring end to end user integration.
+ Lead the onboarding of new production lines to the manufacturing facility.
**Education & Years of Experience:**
+ Third level qualification in engineering/ Science/ Manufacturing/ Supply Chain discipline.
+ Two years work experience in an engineering/ manufacturing environment preferred.
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

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X ( , Facebook, Instagram ( , YouTube and LinkedIn.
Job Description
Our pipeline holds the promise of medicines and solutions that could treat 1.6+ billion people. Learn more about bringing this promise to life.
Welcome to AbbVie!
AbbVie employees work every single day to discover and address many of the world's most pressing health challenges. Our work helps people live better lives. When you have patients depending on your solutions, you look for the best people, and when we find them, we make it our business to treat them well.
Our Westport team invites technical experts to join our NPI Biopharma operations team as our new Technical Shift Leader. In the role, you will have the opportunity to lead an established team developing and guiding its members technically and professionally.
This is a shift based role, you will be required to work 12-hour shifts between days and nights on a monthly rotation.
Delivering high levels of customer service, in this role, you will ensure the quality of the product, comply with all regulatory requirements, achieve desired financial performance, including cost reductions, and build a high-performance culture for the team.
If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more:
Key activities:
+ Act as your team's key point of contact and technical expert.
+ Lead and support your team to deliver compounding, filling, lyophilization, equipment preparation, formulation, buffer preparation and processing activities in the biologics fill-finish facility to meet clearly stated operating objectives
+ Coach & mentor your manufacturing team to maximize its effectiveness through clear and effective communication
+ Promote and develop a culture of contamination control and compliance with aseptic best practices
+ Communicate departmental goals to provide cost-effective quality compliant products in a safe, effective manner
+ Collaborate with program management, supply chain, technical operations, quality, and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing
+ Resolve operations/project issues with team members, project customers, and others as appropriate.
+ Drive operations excellence and key operations targets, including OEE where applicable
+ Provide direct interface as a subject matter expert with the QA department to interact with HPRA, FDA and applicable health authorities and internal audits.
Qualifications
So what will you need to be successful in this role?
Education and preferred experience:
+ Minimum of 5 years experience in batch processing, automation, commissioning, and/or validation in an FDA/HHPRA-regulated industry.
+ Bachelor's degree in chemistry, pharmacy, engineering or a related scientific field is required; an advanced degree is preferred.
+ Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
+ Comprehensive understanding of contamination control principles and regulatory expectations for aseptic processing.
+ Technical background in pharmaceutical, biologics, or similar industries.
+ A minimum of 1 year of direct supervisory experience in a team environment is preferred
+ Possess strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors. Exercises judgment and advises the appropriate actions
Additional Information
All your information will be kept confidential according to EEO guidelines.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Req ID:
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: Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway A career at Celestica is only for those who want to do something extraordinary with a meaningful purpose: imagine, develop and deliver a better future with our customers. Celestica is a leader in high - reliability design, manufacturing and supply chain solutions that bring global expertise to every stage of product development. By Joining Celestica Galway (Ireland) as a Senior Lead Engineer, Manufacturing Process Engineer you will have the opportunity to work on delivering a fully automated high volume manufacturing line from development stage to full scale production ramp producing world class medical devices in a dynamic, fast moving environment. This position offers a great opportunity for a Senior Lead Engineer to work in a dynamic and challenging environment of high speed automation for micro assemblies across our business in the Automated Technology Solutions & Health-tech (Medical Device) market. Your next challenge will be. To become responsible for designing, developing, deploying and optimizing processes for manufacturing to achieve quality, cost and delivery goals for Celestica and its customer's products. This role provides support and ongoing development to a complex high speed automated production line and new product introductions. This position will be responsible for supporting some of our product family in the ATS & Medical Device markets working closely with the operations, technical and quality teams and product designers to drive projects that continually improve the line performance as well as solution and provide input to new business opportunities. The position will report into our Engineering Manager. Your day to day activities will include the following. Being responsible for understanding and implementing the customer's technical roadmap and related process development projects. Leading and implementing the development and release of the full manufacturing process for new customer products. Understanding and providing feedback on customer's technical requirements to team members and management Developing and implementing costed and optimized feedback using Design for manufacturability (DFX) tools and processes, with the goal of reducing manufacturing cost and improving quality and reliability of product. Developing, planning and leading the assessment of the capability of process applications using the design of experiments. Devising process controls and data collection strategies and evaluating complex data to assist with reporting yield, reliability and diagnoses to root causes failures impacting product quality. Enabling Competencies: Project Management - Ability to manage/lead complex, multiple line engineering projects that may also involve other functions. Demonstrate solid understanding of the technical, financial and people aspects of the project. Able to create a project/change management plan and ensure that the project is delivered within the assigned time and budget. Ability to recognize project barriers and develop mitigation plans Leadership - Demonstrate "People & Team Leadership Behaviours" as per Celestica Leadership Imperatives. Financial Acumen / Business Planning - Ability to create financial plans for your projects, align them internally with your line of management and other functions and externally if needed. Create project plans, profitability calculations, risk and sensitivity analysis, able to recognize barriers and mitigate profitability risks. Fully knowledgeable about internal and external financial reporting, accounting and tax requirements relevant to your area of expertise. The following competencies may also be required: Coaching/Mentoring; Communication/Negotiation/Presentation; Creative Problem Solving; Customer Interaction/Stakeholder Management; Quality & Lean; Working Effectively with Others; D/PFMEA; 8D/Corrective Action; Equipment Safety; Design of Experiments (DOE). Technical Competencies: NPI-PCBA: ESD, Component Prep, Laser marking, Solder Paste Deposition (screening / jetting) / Stencil Design, SMT component placement, Reflow, Tooling design, PTH soldering, PTH manual assembly, Press Fit assembly, Depanelization, Board level mechanical assembly, wire harness assembly, wire prep, SMT data analytics, SMT / PTH manual / automated rework, cleaning processes, coating / potting underfill / ruggedization processes, pack & ship, optical component assembly, fiber / tray handling processes, fiber splicing, IPC-610, quality data (KPI), Engineering Control & System Tools (ODC/SCE), Manufacturing Operational management, DFM - Mfg, DFA, DFR, Customer specific processes, structural test and inspection processes, machining, welding, CNC programming, secondary processes, sheet metal, DFAA. DFX: ESD Controls, Component Prep, Component Module Programming, Laser Marking, Screening, Stencil Design, Solder Paste Dispense / Jetting, SMT Programming, SMT Placement, SMT Reflow, Sweat Soldering, Flex Board Assembly / Handling, Pallet Design, PTH Soldering, Robot Soldering, PTH manual Assembly, PTH Auto Assembly, Pressfit, Depanelization, Mechanical Assemb;y (TIMs, Heatsinks, PCBA, Hotbar, Ultrasonic Welding), Wire Harness Assembly, Wire Prep, System Assembly, SMT and PTH Rework, Cleaning Processes, Conformal Coating, Underfills / Edgebonding / Potting, Pack and Ship, Chassis Assembly (fluidics, electrical enclosure, cable routing), Sheet Metal , Machining, Welding, Structural Test (API, AOI, AXI, ICT, Flying Probe) FA LAB : ESD Controls, Solder Metallurgy, Strain Gauge Analysis, SIR Testing, Solder Joint Reliability Modeling, Sample Prep (Grind and Polish), Dye & Pry, CMM/VMM, Lab X-Ray, Pull/Bend Testing, Vibration Testing, Drop Testing, TDR, XRF, SEM, FTIR, IC, Solderability Testing, Thermal Analysis, HALT/HASS, TH&B, Thermal Shock, ATC OPTICAL & XRAY INSPECTION: ESD Controls, Auto Wire Prep, SMT Data Analytics, API, AOI (PCBA), AXI (PCBA), AOI (System), Test Strategy Creation, IPC-610, Quality Dat (KPI), DFM - Manufacturing, DFA - Assembly, DFT / Physical Test, DFT - Electrical Test MACHINING & OTHER: ESD Controls, Pack & Ship, CNC programming, Secondary Processing, Sheet Metal, Machining, Welding, DFM - Manufacturing MECHANICAL & SYSTEMS ASSEMBLY: ESD Controls, Wire Harness Assembly, Auto Wire Prep, Mechanical Assembly - System Build, OEE / Industrial Engineering, Pack & Ship, Vacuum System, Fluidics, Electrical Enclosure, Cable Routing, Electrical - Automation, Mechanical - Automation, Machine Vision, IPC-610, Engineering Controls, Quality Data (KPI), Manufacturing Operational Management, DFM - Manufacturing, DFA - Assembly, DFAA - Automated Assembly, DFT - Physical Test MICROELECTRONICS: ESD Controls, Wafer Thinning, Wafer Singulation, Edge Polishing, Optical Coatings, Die Bonding, Vacuum Reflow, Flip Chip Bonding, Underfill, Active Alignment, Plasma Cleaning, Wire Bonding, Encapsulation, Sealing, Leak Testing, Interconnect Formation What do we offer? Market-competitive total reward: flexible salary, fix and variable salary based on goals The opportunity to become a key member of the new product introduction team in the Health Tech. Engineering function driven by innovation where creativity matters. Training and development opportunities, with us the sky is the limit! The opportunity to innovate, learn, mentor others and work toward your own vision of career success A global, collaborative culture with strong leadership imperatives to foster your growth and professional opportunities A sustainable culture where we provide opportunities for employees to give back to the community What do we expect from you? Excellent Project Management and Time Management skills Excellent communication Skills both written and verbal. Experience creating CAPA, FMEA, SOP's, Control Plans and performing validation (FAT, SAT, IQ, OQ, PQ). Ability to effectively communicate manufacturing plans, proposals, results, and negotiate options at management levels. Strong analytical and problem solving skills. Excellent interpersonal & communication skills. Strong report writing & data analytical capabilities. Advantageous to have knowledge of the medical device industry and of 21 CFR, (820, 11), ISO13485, specifically in the areas of Change Control and Validation. What are we looking for? Someone with a Degree in Engineering with 4+ years' relevant experience Relevant Medical DeviceAND/ORAutomation experience preferred Experience in ISO13485 medical device manufacturing environment is desirable. Relevant project management experience and associated qualifications with NPI experience Someone with an ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically and make sound decisions Someone that is open to the opportunity of short term travel assignments particularly at the early stages of the project. Someone that has excellent customer Management skills and a knowledge of customer and regulatory requirements. Someone that has previous experience of coaching and mentoring junior engineers. Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law). At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them. COMPANY OVERVIEW: Celestica (NYSE, TSX: CLS) enables the world's best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development - from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers. Celestica would like to thank all applicants, however, only qualified applicants will be contacted. Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services. To Apply Please forward your CV via the APPLY Now button below.

Req ID: 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; 8 D/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/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, Health Tech, 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.