57 Car Systems jobs in Ireland

**Summary:**
The RTP team is responsible for the end-to-end Hardware Lifecycle of all Meta servers, from exploration and development to production health. We work closely with various teams to ensure the smooth operation of systems across the planet, troubleshooting complex issues at various scales, from microscopic to fleet-wide, and driving projects to successful business outcomes.
**Required Skills:**
Production Systems Engineer Responsibilities:
1. Build and develop tooling solutions to automate business critical processes in service of managing the health of the Meta production fleet
2. Troubleshoot, diagnose and root cause system failures, working with key partners to identify and deliver solutions
3. Proactively identify opportunities to fix or enhance tooling, hardware and processes
4. Build subject matter expertise in one or more of the specialist areas covered by the RTP (Reliability and Testability Platform) team in Dublin - Firmware Deployment
5. Scientific approach to troubleshooting, root-cause analysis and investigation
**Minimum Qualifications:**
Minimum Qualifications:
6. Bachelors degree in computer science, a related technical discipline, or equivalent work experience
7. Experience coding in a higher-level language (Python, PHP, Java, Go, Rust, C++)
8. Experience building, maintaining and debugging production services or platforms - usually but not necessarily in a Linux/Unix environment
9. Edge/CDN (Content Delivery Network) hardware or Silicon Sustainment
**Preferred Qualifications:**
Preferred Qualifications:
10. 8+ years experience coding in a higher-level language (Python, PHP, Java, Go, Rust, C++)
11. Knowledge of server architecture and components across Compute/Storage/AI Systems/Networking
12. Demonstrated experience in communication and collaboration
**Industry:** Internet

**Summary:**
Meta is seeking a Production Systems Engineer to join our Release to Production (RTP) team in Dublin. Our servers and data centers are the foundation upon which our rapidly scaling infrastructure operates efficiently to deliver our services. The RTP team is responsible for the end-to-end Hardware Lifecycle of all Meta servers, from exploration and development to production health. RTP Engineers work closely with Production Engineering teams, Enterprise Networking, Hardware Designers, Networking Teams, Manufacturers, Vendors, Datacenter Operation teams and New Product Introduction teams to ensure the smooth operation of systems across the planet.As a Production Systems Engineer you will encounter problems from the very smallest of scales (errors occurring at the microscopic scale, within single registers of a CPU) up to the very largest - deploying solutions to our entire fleet. You will manage complex cross-functional demands, and drive a program of work to successful business outcomes. This role will have the chance to work on some of the hardest problems in our domain.
**Required Skills:**
Production Systems Engineer Responsibilities:
1. Manage stakeholder relationships across organization and timezone boundaries
2. Proactively identify opportunities to fix or enhance tooling, hardware and processes
3. Troubleshoot, diagnose and root cause system failures, working with key partners to identify and deliver solutions
4. Build subject matter expertise in Edge/CDN business operations
5. relevant hardware
6. server efficiency and operations
7. Develop tooling and process optimisations to automate business critical processes in service of managing the health of the Meta production fleet
**Minimum Qualifications:**
Minimum Qualifications:
8. Bachelor's degree in technical, scientific or engineering discipline - Computer Science, Physics, Mathematics, or equivalent work experience
9. 6+ years experience of applied analytical techniques, building models and simulations, designing and running experiments
10. Demonstrated experience applying scientific approaches to troubleshoot, investigate, and conduct root-cause analyses
11. Proven technical communication and cross-functional collaboration skills
**Preferred Qualifications:**
Preferred Qualifications:
12. Familiarity with coding in a higher-level language (Python, PHP, Java, Go, Rust, C++)
13. Knowledge of server architecture and components
14. Demonstrated experience of coordinating broad and impactful projects
**Industry:** Internet

Req ID: 126682
Remote Position: No
Region: Europe
Country: Ireland
State/Province: Galway
City: Galway
**General Overview**
**Functional Area:** Quality (QUA)
**Career Stream:** Operations Quality (OPQ)
**Role:** Specialist (SPE)
**Job Title:** Specialist, Operations Quality
**Job Code** : SPE-QUA-OPQ
**Job Level:** Band 08
**Direct/Indirect Indicator:** Indirect
**Summary**
We are currently recruiting for a Systems Quality Engineer as part of our team in Galway.
**Who we are and what we do?**
Celestica is an Equal Opportunities Employer.
Celestica enables the world's best brands. Through our unrivalled customer-centric approach, we partner with leading companies in aerospace and defence, communications, enterprise, health-tech, industrial, capital equipment, and smart energy to deliver solutions for their most complex challenges. With talented teams across North America, Europe and Asia, we imagine, develop and deliver a better future with our customers.
Celestica Galway are a leader in automated manufacturing services with proven expertise in delivering scalable manufacturing solutions throughout the product lifecycle. Celestica Galway supports and provides Automated Technology Solutions & Health-tech Solutions for a number of customers including the Medical Device space.
**Your next challenge will be.**
Lead process/procedure definition and maintain a continuous flow of high-quality products to our customers in a contract manufacturing environment including regulatory content for the latest and more innovative medical devices. This position will be responsible for supporting some of our product family in both the Med tech and Industrial sectors liaising with Production, Engineering, Supply Chain and Customer contracts reporting into our Quality Manager.
**Detailed Description**
Your day-to-day activities will include the following.
+ Manage performance of reports
+ Customer liaison for quality escalations and daily quality issues ensuring measured, developed and timely responses to the customer.
+ Support the change management process and Customer requests as appropriate.
+ High level of competence using relevant corrective action systems (e.g., CAPA)
+ Create concise and accurate technical reports, communicate results and manage subsequent analysis queries
+ Continually seek to drive improvements in product and process quality.
+ Create and evaluate metrics to drive the quality improvement processes.
+ Own, Maintain and report timely and accurate KPI's
+ Create, and update, Procedures and Work Instructions
+ Manage and maintain the NCMR database and report weekly to the customer.
+ Using appropriate statistical techniques to monitor process performance (e.g.SPC, Minitab, Ppk, Gage R & Ranalysis, sampling techniques).
+ Provide quality engineering support to the facility, including validation and risk management and review of technical documentation (eg. FMEA's, control plans)
+ Ability to design tests, evaluate results and recommend solutions to improve the processes associated with our manufacturing.
**Conditions of Employment**
+ Market-competitive total reward: Company Performance bonus program, company pension and health insurance.
+ The opportunity to become a key member of the new product introduction team in the Health Tech Quality function driven by innovation where creativity matters.
+ Training and development opportunities, with us the sky is the limit!
+ The opportunity to innovate, learn, mentor others and work toward your own vision of career success
+ A global, collaborative culture with strong leadership imperatives to foster your growth and professional opportunities
+ A sustainable culture where we provide opportunities for employees to give back to the community
**Knowledge/Skills/Competencies**
+ Strong knowledge of quality tools, ISO / QMS standards and processes (ISO 9001, ISO13485)
+ Knowledge of data analysis and presentation software and its uses in generating reports, capturing data and presenting data in an understandable format.
+ Strong knowledge of product and manufacturing processes and materials properties
+ Knowledge and understanding of the manufacturing environment and how decisions impact customer satisfaction product quality, on-time delivery and profitability of the unit
+ Knowledge of quality tools such as FMEA, PMP, SPC, 8D methodology, etc.
+ Knowledge of Six sigma and Lean Kaizen.
+ Ability to effectively communicate with a wide variety of internal and external customers to summarize complex technical issues
+ Knowledge of Med-tech and regulatory requirements (such as FDA and MDR) is a requirement of the role with pharma & food safety systems an advantage
+ Ability to effectively lead and manage several projects simultaneously and coordinate multiple, changing deadlines while also working effectively on their own and in a team environment.
+ Ability to be an Internal Auditor
**Typical Education**
+ Bachelor's degree in related field
+ 6 years or more experience in a manufacturing environment within a Quality function
+ Experience in a Med-tech environment is essential
+ Experience of 6 Sigma quality methods would be a distinct advantage.
+ Materials engineering experience/quality materials testing knowledge is an advantage
+ Experience of leading a team is an advantage.
**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.

**Job Description Summary**
BD's Medication Management Solutions (MMS) division seeks a Senior Systems Engineer for the growing Pharmacy Automation team, developing innovative technology for pharmacies.
The Senior Systems Engineer will drive the design and validation of complex systems, collaborating with cross-functional teams.
**Job Description**
**We are the makers of possible**
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
**Why join us?**
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
**Become a maker of possible with us!**
**Our vision for Medication Management Solutions at BD**
With our technical capabilities, the Medication Management Solutions (MMS) team are able to manage multiple systems and our operational capabilities enable us to have medications available when and where needed, reducing inefficiency and waste for nursing and pharmacy teams.
**About the role**
BD's Medication Management Solutions (MMS) division is seeking a Senior Systems Engineer to join its rapidly expanding Pharmacy Automation team. This strategic area of growth empowers BD to deliver comprehensive, integrated solutions to pharmacy customers, addressing critical industry challenges such as clinician shortages and healthcare worker burnout. The role focuses on the development of cutting-edge pharmacy automation technologies-including robotic systems, packaging and dispensing solutions, and enterprise software-designed to streamline operations across centralized and decentralized pharmacy settings.
As a key technical contributor, the Senior Systems Engineer will lead the definition, design, and verification of complex systems that integrate electromechanical hardware and software components. The role involves deriving product requirements from user needs, developing system specifications, performing risk assessments (such as dFMEA), and executing verification and validation activities. Leveraging methodologies such as Design for Six Sigma (DFSS) and both Agile and Waterfall development models, the engineer will collaborate closely with cross-functional teams, including mechanical, software, reliability, and quality engineering. This role also supports transitioning designs from R&D into manufacturing and provides technical expertise for field troubleshooting and quality assurance initiatives.
**Main responsibilities will include:**
+ Provides technical solutions to a wide range of difficult problems. Solutions are imaginative, thorough, practical, and consistent with objectives. Exercises latitude in determining technical objectives of the assignment methods and in selecting techniques and evaluation criteria for obtaining resolution based on risk-based assessment (including dFMEA analysis and input into product Hazard Analysis).
+ Contributes to the completion of specific programs and projects, and develops work plans to reduce concept to design.
+ Owns derivation & test of product requirements and high-level design system and subsystem specifications. This includes derivation from user needs, writing, tracing, characterizing, and verifying specification performance.
+ Assumes a technical contributor role and works closely with other functional groups. Will provide guidance and work direction to cross-functional team members including mechanical engineers, reliability engineers, software developers, and software test.
+ Independently evaluates problems of high complexity and applies analytical/scientific principles to fulfill project and business objectives. Designs and performs development activity independently with minimal supervision.
+ Development of detailed subsystem workflow step and exception logic to guide software in development of instrument functions as well as to inform Theory of Operation for product/solution.
+ Collects, records, analyzes, interprets, reports, and, presents results to cross functional colleagues and leaders.
+ Responsible for employing DFSS (Design for Six Sigma) and product development best practices to manage technical risk and impart product robustness and reliability.
+ Execute system verification and validation activities for their cross-functional project team including protocol writing, execution and reporting.
+ Contributes to the transition from R&D to manufacturing/service and supports system troubleshooting activities for products in the field.
+ Liaison between R&D and Quality/Reliability functions to inform/support functions based on quality procedures including risk analysis, verification/validation for specific subsystems.
**About you**
+ Must have a bachelor's degree in science or engineering.
+ A minimum of 6 years relevant experience in systems engineering, medical device design, robotic system design or similar.
+ Experience with Systems Engineering and requirements management, including:
+ Demonstrated capability with requirement/specification management
+ Systems integration and testing, Failure Modes Effects Analysis, verification & validation
+ Experimental design, data acquisition, graphical analysis and use of statistical methods for large complex data sets. Experience implementing Design for Six Sigma (DFSS) methodologies.
+ Beta-testing, and/or field implementation of new product launches preferred.
+ Ability to work independently and as a member of a multi-disciplinary team, with global collaboration and external development partners.
+ Ability to communicate concepts, ideas and knowledge effectively and clearly to other individuals and teams.
+ Experience operating in at least 1 product development process: waterfall or agile; experience operating within design control.
+ A differentiator would be an understanding of or experience working in outpatient, retail, and/or central pharmacy.
**Click on apply if this sounds like you!**
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.
**To learn more about BD visit:** ** Skills
Optional Skills
.
**Primary Work Location**
IRL Limerick - Castletroy
**Additional Locations**
**Work Shift**
At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You ( .
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed.
The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.
**Salary Range Information**
54,800.00 - 93,200.00 EUR Annual
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

R&D Engineer - Limerick. As Systems Engineer you will contribute to cross-disciplinary product development teams and lead the definition, design, and execution of Systems Engineering activities throughout all phases of the product lifecycle. You will plays a critical role in leading systems engineering efforts for both new product development (NPD) and released products. This position is responsible for developing and maintaining system and product design architectures, ensuring system-level requirements are properly documented and managed, and leading the definition of system interfaces. The engineer ensures traceability from user needs to test evidence, supports configuration management, and drives integration and defect tracking efforts. Additionally, they oversee system evaluation processes, including test planning, execution, and data analysis, while facilitating collaboration between R&D, Quality, and Reliability teams to resolve technical challenges. Main responsibilities will include: Ownership of Systems Engineering inputs and outputs for teams supporting either NPD or released product. Responsibility for development and maintenance of system/product design architecture and system/product requirements. Document system/product-level requirements and managing changes via team review, approval, and release process. Lead the definition and documentation of system interfaces and interface requirements. Ensure design traceability from user needs through requirements to test evidence and supports the use of appropriate software tools for the creation and maintenance of the trace matrices. Lead system/product-level integration, bug/defect tracking and configuration management. Lead the system evaluation process through development and execution of system level test plans and protocols including data analysis, interpretation and communication of results and their impact through written reports, design reviews, and interactive discussions. May lead system verification and validation activities for a multi-functional project team including protocol writing, execution and reporting. Contribute to the transition from R&D to manufacturing/service and supports resolving system issues for products in the field. Liaison between R&D and Quality/Reliability functions to inform/support functions based on quality procedures including risk analysis, verification/validation for specific subsystems. Critically assesses designs and test plans through robust Technical and/or Design Reviews. Facilitates broad perspectives, knowledge and experiences to promote the understanding and resolution of in-market and product development issues. Provide technical solutions to a wide range of difficult problems. Exercises latitude in determining technical objectives of the assignment methods and in selecting techniques and evaluation criteria for obtaining resolution using risk-based assessment (including dFMEA analysis and input into System Hazard Analysis). Interested applicants should have: An extensive background in electro-mechanical medical device product development, IVD device development, or lab automation development. A strong technical background and experience within Systems Engineering Requirements Management, Hazards Analysis, System Architectural Development, Functional Modelling, Systems Integration, Statistical Test Design, Verification and Validation, Reliability Engineering, and Failure Modes Effects Analysis. Lead complex experiments independently, perform statistical analysis, interpret experimental results, and make sound conclusions. Apply creative problem-solving skills to novel or complex applications. Ability to self-direct and manage own work while possessing strong interpersonal skills with the ability to collaborate in multi-disciplinary team settings, influence decision-making, and build group consensus. Perform in a fast-paced, agile environment. Collaborative leader committed to success of overall project; capable of encouraging others and leading without authority. Proven technical expertise and leadership in medium to large sized projects, with the ability to meet technical objectives and solve sophisticated challenges under conditions of ambiguity and rapid change. Strong problem-solving and debugging skills and an interest in learning new technologies. "Self-starter" mentality and the ability to make decisions. Excellent written and oral communication skills.) Skills: system engineering medical device product development IVD

Req ID: 126682 Remote Position: No Region: Europe Country: Ireland State/Province: Galway City: Galway General Overview Functional Area: Quality (QUA) Career Stream: Operations Quality (OPQ) Role: Specialist (SPE) Job Title: Specialist, Operations Quality Job Code: SPE-QUA-OPQ Job Level: Band08 Direct/Indirect Indicator: Indirect Summary We are currently recruiting for a Systems Quality Engineer as part of our team in Galway. Who we are and what we do? Celestica is an Equal Opportunities Employer. Celestica enables the world's best brands. Through our unrivalled customer-centric approach, we partner with leading companies in aerospace and defence, communications, enterprise, health-tech, industrial, capital equipment, and smart energy to deliver solutions for their most complex challenges. With talented teams across North America, Europe and Asia, we imagine, develop and deliver a better future with our customers. Celestica Galway are a leader in automated manufacturing services with proven expertise in delivering scalable manufacturing solutions throughout the product Galway supports and provides Automated Technology Solutions & Health-tech Solutions for a number of customers including the Medical Device space. Your next challenge will be. Lead process/procedure definition and maintain a continuous flow of high-quality products to our customers in a contract manufacturing environment including regulatory content for the latest and more innovative medical devices. This position will be responsible for supporting some of our product family in both the Med tech and Industrial sectors liaising with Production, Engineering, Supply Chain and Customer contracts reporting into our Quality Manager. Detailed Description Your day-to-day activities will include the following. Manage performance of reports Customer liaison for quality escalations and daily quality issues ensuring measured, developed and timely responses to the customer. Support the change management process and Customer requests as appropriate. High level of competence using relevant corrective action systems (e.g., CAPA) Create concise and accurate technical reports, communicate results and manage subsequent analysis queries Continually seek to drive improvements in product and process quality. Create and evaluate metrics to drive the quality improvement processes. Own, Maintain and report timely and accurate KPI's Create, and update, Procedures and Work Instructions Manage and maintain the NCMR database and report weekly to the customer. Using appropriate statistical techniques to monitor process performance (e.g.SPC, Minitab, Ppk, Gage R & Ranalysis, sampling techniques). Provide quality engineering support to the facility, including validation and risk management and review of technical documentation (eg. FMEA's, control plans) Ability to design tests, evaluate results and recommend solutions to improve the processes associated with our manufacturing. Conditions of Employment Market-competitive total reward: Company Performance bonus program, company pension and health insurance. The opportunity to become a key member of the new product introduction team in the Health Tech Quality function driven by innovation where creativity matters. Training and development opportunities, with us the sky is the limit! The opportunity to innovate, learn, mentor others and work toward your own vision of career success A global, collaborative culture with strong leadership imperatives to foster your growth and professional opportunities A sustainable culture where we provide opportunities for employees to give back to the community Knowledge/Skills/Competencies Strong knowledge of quality tools, ISO / QMS standards and processes (ISO 9001, ISO13485) Knowledge of data analysis and presentation software and its uses in generating reports, capturing data and presenting data in an understandable format. Strong knowledge of product and manufacturing processes and materials properties Knowledge and understanding of the manufacturing environment and how decisions impact customer satisfaction product quality, on-time delivery and profitability of the unit Knowledge of quality tools such as FMEA, PMP, SPC, 8D methodology, etc. Knowledge of Six sigma and Lean Kaizen. Ability to effectively communicate with a wide variety of internal and external customers to summarize complex technical issues Knowledge of Med-tech and regulatory requirements (such as FDA and MDR) is a requirement of the role with pharma & food safety systems an advantage Ability to effectively lead and manage several projects simultaneously and coordinate multiple, changing deadlines while also working effectively on their own and in a team environment. Ability to be an Internal Auditor Typical Education Bachelor's degree in related field 6 years or more experience in a manufacturing environment within a Quality function Experience in a Med-tech environment is essential Experience of 6 Sigma quality methods would be a distinct advantage. Materials engineering experience/quality materials testing knowledge is an advantage Experience of leading a team is an advantage. 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.

Location - Westport, Mayo Role title: Operational Technology Systems Engineer (Pharma) Join our team and help bring innovation in the lifesciences sector. We're seeking an OT Systems Engineer to help with regulatory compliance, data integrity, and process automation. What You'll Do: OT System SCADA Engineer role supports lifecycle management of Operational TechnologySystems & applications across the Westport Manufacturing Site. The OT Systems Engineer willbe expected to support all aspects of the Production OT systems and provide development andinstallation support for new hardware and software solutions. Key responsibilities: Responsibilities: Support of Operating System platforms and OT software applications Provision of technical support and direction to Manufacturing Operations, Validation Engineers, and IT support staff as part of Manufacturing project support and project execution including transfer to production. Provision of support for root cause problem solving and the implementation of CAPA's. Assist with design and build of secure, robust, highly available fit-for-purpose and future proofed application environments. Follow the OT lifecycle management processes that meet or exceed regulatory expectation in respect of data integrity: data backup regimes and system recovery testing. Creation of technical documents required to complete SDLC document set, and knowledge articles required by Tier 2 and Tier 3 support teams. Support any safety or quality initiatives that require Operational Technology support. Support cost savings initiatives onsite and within the Automation team Participate in departmental and customer project status update meetings. Support operational excellence activities to continuously improve our processes and eliminate waste. Qualifications: Bachelor's degree in information technology, Computer Engineering, or related discipline / equivalent experience. 3 to 5 years' experience delivering IT services preferably within the Pharmaceutical and/or medical device industry. System Admin Windows 10 and Windows Server Expertise in the following technologies: SCADA, Historian, Thin Client Manager, Active Directory and group policy permissions, XML/XSL, SQL DBA and the development of SQL Queries, Stored Procedures and Reporting. Extensive experience delivering automation projects (PLC and SCADA). Aseptic processing and or packaging equipment experience. Experience with delivering complex projects, ideally related to manufacturing modernization / manufacturing system upgrades to support business critical process equipment. Employment type: Full-time Work location: Onsite To start the process click the Continue to Application or Login/Register to apply button below.

Job Description Summary BD's Medication Management Solutions (MMS) division seeks a Senior Systems Engineer for the growing Pharmacy Automation team, developing innovative technology for pharmacies. The Senior Systems Engineer will drive the design and validation of complex systems, collaborating with cross-functional teams. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. Why join us? A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place. Become a maker of possible with us! Our vision for Medication Management Solutions at BD With our technical capabilities, the Medication Management Solutions (MMS) team are able to manage multiple systems and our operational capabilities enable us to have medications available when and where needed, reducing inefficiency and waste for nursing and pharmacy teams. About the role BD's Medication Management Solutions (MMS) division is seeking a Senior Systems Engineer to join its rapidly expanding Pharmacy Automation team. This strategic area of growth empowers BD to deliver comprehensive, integrated solutions to pharmacy customers, addressing critical industry challenges such as clinician shortages and healthcare worker burnout. The role focuses on the development of cutting-edge pharmacy automation technologies-including robotic systems, packaging and dispensing solutions, and enterprise software-designed to streamline operations across centralized and decentralized pharmacy settings. As a key technical contributor, the Senior Systems Engineer will lead the definition, design, and verification of complex systems that integrate electromechanical hardware and software components. The role involves deriving product requirements from user needs, developing system specifications, performing risk assessments (such as dFMEA), and executing verification and validation activities. Leveraging methodologies such as Design for Six Sigma (DFSS) and both Agile and Waterfall development models, the engineer will collaborate closely with cross-functional teams, including mechanical, software, reliability, and quality engineering. This role also supports transitioning designs from R&D into manufacturing and provides technical expertise for field troubleshooting and quality assurance initiatives. Main responsibilities will include: Provides technical solutions to a wide range of difficult problems. Solutions are imaginative, thorough, practical, and consistent with objectives. Exercises latitude in determining technical objectives of the assignment methods and in selecting techniques and evaluation criteria for obtaining resolution based on risk-based assessment (including dFMEA analysis and input into product Hazard Analysis). Contributes to the completion of specific programs and projects, and develops work plans to reduce concept to design. Owns derivation & test of product requirements and high-level design system and subsystem specifications. This includes derivation from user needs, writing, tracing, characterizing, and verifying specification performance. Assumes a technical contributor role and works closely with other functional groups. Will provide guidance and work direction to cross-functional team members including mechanical engineers, reliability engineers, software developers, and software test. Independently evaluates problems of high complexity and applies analytical/scientific principles to fulfill project and business objectives. Designs and performs development activity independently with minimal supervision. Development of detailed subsystem workflow step and exception logic to guide software in development of instrument functions as well as to inform Theory of Operation for product/solution. Collects, records, analyzes, interprets, reports, and, presents results to cross functional colleagues and leaders. Responsible for employing DFSS (Design for Six Sigma) and product development best practices to manage technical risk and impart product robustness and reliability. Execute system verification and validation activities for their cross-functional project team including protocol writing, execution and reporting. Contributes to the transition from R&D to manufacturing/service and supports system troubleshooting activities for products in the field. Liaison between R&D and Quality/Reliability functions to inform/support functions based on quality procedures including risk analysis, verification/validation for specific subsystems. About you Must have a bachelor's degree in science or engineering. A minimum of 6 years relevant experience in systems engineering, medical device design, robotic system design or similar. Experience with Systems Engineering and requirements management, including: Demonstrated capability with requirement/specification management Systems integration and testing, Failure Modes Effects Analysis, verification & validation Experimental design, data acquisition, graphical analysis and use of statistical methods for large complex data sets. Experience implementing Design for Six Sigma (DFSS) methodologies. Beta-testing, and/or field implementation of new product launches preferred. Ability to work independently and as a member of a multi-disciplinary team, with global collaboration and external development partners. Ability to communicate concepts, ideas and knowledge effectively and clearly to other individuals and teams. Experience operating in at least 1 product development process: waterfall or agile; experience operating within design control. A differentiator would be an understanding of or experience working in outpatient, retail, and/or central pharmacy. Click on apply if this sounds like you! At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.

About Viska Systems: At Viska Systems, were not just transforming industries, were shaping the future of AI and automation. As a company recognised for excellence and innovation and named Best AIPowered Machine Vision & Robotics Company 2025 by the Irish Enterprise Awards, wespecialise in seamlessly integrating Machine Vision, Robotics, and Software Development to deliver innovative automated inspection systems that enhance product quality and improve operational efficiency. Were looking for an Automation Systems Engineer to join our team in Cork. This is your opportunity to play a key role in shaping the future of AI and machine vision and drive efficiency across industries. Technical Responsibilities Embedded Software Development: Build robust applications across front-end and back-end platforms, with emphasis on scalability and maintainability. Work with Gstreamer pipelines, open-source vision models, Git, and Docker. Optimise hardware use for machine vision workloads, and support the full development cycle, bringing code from prototype through testing into production. Code Quality, Version Control, & Deployment: Write efficient, testable code and manage repositories using Git, and deploy using tools like Docker. Production Control: Identify and resolve critical bugs and production issues quickly and independently. System Assembly Lead the build of machine systems, guiding technicians through both mechanical assembly and electrical wiring. Project Documentation Accurately complete ISO9001 documentation, including requirement specs, bills of materials, and testing and reporting records. Team Leadership Provide technical leadership by onboarding and mentoring new team members, including acting as a lead for junior engineers. What Were Looking For Software Development Expertise: 5+ years in a hands-on systems engineering role using Python, ideally in a startup or small-team environment. Proven experience owning production-grade systems from design through deployment and support. Educational Background: Masters Degree in Computer Engineering, or Mechatronics / Electronics or a related technical field. Specialised Knowledge: AI technologies, machine learning frameworks, open-source vision tools such as OpenCV and YOLO. Software Development Methodologies: Experience with Agile or Scrum processes. Software Tools: Experience with GIT and Docker. Initiative: Proven ability to work independently and show initiative in a fast-paced environment. Mentorship: Experience supporting or mentoring junior engineers. DevOps: Familiarity with DevOps practices and tools (e.g., Git, CI/CD, Docker) is an advantage. Why Work for Us? At Viska Systems, we offer a dynamic environment where your contributions directly impact our success: Competitive Compensation: A strong starting salary with a comprehensive benefits package. Career Advancement: Structured mentorship and clear pathways for career development in software engineering. Cutting-Edge Technology: Work on innovative, award-nominated AI solutions that are shaping the future of manufacturing and automation. Training & Development: Access to ongoing training to deepen your technical expertise in AI, machine vision, and software development. Collaborative Team Culture: Join a dynamic and supportive team that values your ideas and contributions. Ready to Join Us? Take the next step in your career with Viska Systems and become part of a company at the forefront of AI-driven innovation. Please note, you must be eligible to work in Ireland.