As a result of the combination of the BD Biosciences and Diagnostic Solutions business with Waters Corporation (NYSE: WAT), by applying to this role, you will be applying for a position with Waters. Waters is a global leader in life sciences, dedicated to accelerating the benefits of pioneering science through analytical technologies, informatics, and service. With a focus on regulated, high-volume testing environments, Waters' innovative portfolio harnesses deep scientific expertise across biology, chemistry, and physics. Waters collaborates with analytical laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combatting growing antibiotic resistance. Through a shared culture of relentless innovation, Waters' passionate team of approximately 16,000 colleagues partner with customers to turn scientific challenges into breakthroughs that improve lives worldwide. We are the people who give possibilities purpose 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. Job Description About the Role As part of the Systems Engineering group, our Senior Systems Engineer will have a phenomenal opportunity in providing their system knowledge to lead and contribute to the Waters portfolio of products. This role entails utilizing your detailed understanding of system design and system integration tools and methodologies to connect pieces across the different functional elements i.e. Software, Mechanical, Electrical, Fluidics, Biochemistry and Optical engineering. You will ensure the product requirements are defined/maintained and the lower-level functional design teams deliver them to those requirements. Job Responsibilities: Coordinate system-level product development; system architecture, integration, and system characterization testing Exercise strong Communication and Leadership skills to collaborate with Waters worldwide teams, including Waters external partners. Provide technical support to a wide range of problems pertaining to specific programs and projects. Consistently apply Systems Engineering Techniques such as requirements management, traceability, risk management, Verification and Validation. Work effectively in a multi-functional team, in a collaborative manner to identify, communicate and mitigate project/program needs based on lifecycle phase. Apply focused work methodologies utilizing scientific and statistical methods (six sigma) in resolving problems, devising tests and setting specifications. Minimum Qualifications Education and Experience: Minimum of a Bachelor's Degree required; ideally in BioEngineering, BioMedical, Biology, Chemical Engineering. Masters or PhD degree prefered. Minimum of 5 years' experience in systems engineering, product development, or product design with Bachelor degree, 3 years with Masters degree, 2+ years with PhD Experience developing and executing System Level Characterization, Integration or Test Procedures. Knowledge and Skills: Experience with Flow Cytometry is desirable for this role Experience or good understanding of immunology is a plus Experience in Product Development for In Vitro Diagnostic and/or medical devices in ISO 13485 environment. Experience with Risk Management methodology Proficiency in the use of Traceability tools such as JIRA,DOORS or Azure. Good understanding of Structured Product Development Process and methodology. Experience with Engineering Change Management procedures post commercialization of products such as ECOs, engineering change impact assessments, regression testing assessments etc. Software and script language programming skills is a plus. Salary Range: €65K - €70K + Bonus + Benefits Why Join Us? 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 healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success. TPBN1_IJ
As a result of the combination of the BD Biosciences and Diagnostic Solutions business with Waters Corporation (NYSE: WAT), by applying to this role, you will be applying for a position with Waters. Waters is a global leader in life sciences, dedicated to accelerating the benefits of pioneering science through analytical technologies, informatics, and service. With a focus on regulated, high-volume testing environments, Waters' innovative portfolio harnesses deep scientific expertise across biology, chemistry, and physics. Waters collaborates with analytical laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combatting growing antibiotic resistance. Through a shared culture of relentless innovation, Waters' passionate team of approximately 16,000 colleagues partner with customers to turn scientific challenges into breakthroughs that improve lives worldwide. We are the people who give possibilities purpose 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. Job Description About the role Serving as a Senior Scientist, you will be instrumental in building the next generation of flow cytometry solutions. You will lead the invention of innovative products that advance our reagent portfolio. Acting as a technical leader and trusted expert, you will develop and implement complex experimental strategies involving reagent systems, assays, workflows, and instruments. You will translate complex data into clear insights that drive product decisions. In close collaboration with cross-functional product development and clinical trial teams, you will ensure solutions uphold technical excellence, customer needs, and regulatory guidelines as applicable. This opportunity allows you to apply independent judgment, critical thinking, and deep scientific expertise to solve complex problems, influence system-level requirements, and present influential findings to both internal teams and external scientific audiences-all while mentoring junior scientists and encouraging a culture of scientific rigor and innovation. Main responsibilities will include: Leading experimental studies in the laboratory and participating in cross-functional discussions to support the program's goals. Demonstrating knowledge of customer workflows, scientific, and technological advancements. Effectively communicating technical concepts/issues of project plans, developing test strategies that balance risk and business objectives, and supporting budget planning based on functional project scope. Leading analysis and presentations of moderate to high complexity at technical reviews. Directing and supervising teams or mentoring junior team members. Acting as a technical contributor on cross-functional core teams, assisting decision-making across functions, and offering input to senior management on strategic and functional decisions. About you MSc or PhD or equivalent experience in Immunology, Cell Biology, Clinical Laboratory Science, or related scientific field with a minimum of 3 years of relevant industry experience. Experience in Flow Cytometry and customer workflows. Proven ability to research and apply scientific principles to develop new or improve existing processes with a focus on hematology, immunology, and/or molecular genetics. Skill in accomplishing complex experiments independently, performing analysis, interpreting experimental results, making sound conclusions, and performing statistical analysis. Creative problem-solving skills to novel or complex applications. Critical evaluation of proposed study builds with knowledge of statistics, calculation of sample sizes, and/or estimation of statistical power. Experience in researching and applying scientific principles to build new or optimize existing laboratory procedures. Ability to train bench-level personnel at multiple levels of education and/or expertise. Strong interpersonal skills with a proven ability to engage effectively with others in multi-disciplinary team settings, guide decision-making, and develop group consensus. Excellent written and oral communication skills. Preferred Qualifications/Capabilities: PhD or equivalent experience and Post-doctoral experience in Immunology/Immuno-oncology and expertise in immunophenotypic analysis of human tissue samples by flow cytometry. Experience in leading small to medium-sized teams of technical contributors. 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. TPBN1_IJ
We are the people who give possibilities purpose 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. Job Description Our vision for Peripheral Intervention at BD Our Peripheral Intervention (PI) business unit offers a comprehensive range of medical products, devices and services for the treatment of peripheral arterial and venous disease, cancer detection, and end-stage renal disease and maintenance. About the role We are seeking a highly skilled and driven Senior Embedded Software Engineer to join our global R&D team in developing embedded software for cutting-edge optoelectronic and electromechanical devices across consumer, industrial, and medical markets. In this role, you will lead the design, implementation, and documentation of board-level firmware in C/C++, contributing throughout the full software development lifecycle. You will work closely with cross-functional teams to translate system-level requirements into embedded system specifications, define interface architectures, and ensure compliance with industry standards such as IEC 62304, ISO 13485, and ISO 14971. Your work will directly impact the performance, reliability, and scalability of safety-critical medical devices. As a key contributor, you will drive software architecture and design reviews, lead integration and testing efforts, and support regulatory submissions and audits. You'll collaborate intensively with electrical, mechanical, systems, quality, regulatory, and clinical teams to deliver robust solutions in a fast-paced, regulated environment. Applying Agile and CI/CD principles, you will help maintain traceability between requirements and test protocols, author and maintain technical documentation, and contribute to configuration management and milestone reviews. This is a unique opportunity to shape life-changing healthcare innovations while working at the forefront of embedded systems engineering. Main responsibilities will include: Translate system-level requirements into embedded system requirements and interface definitions Assess technical feasibility and contribute to embedded system architecture and design concepts Establish embedded hardware and firmware architecture and decompose systems into lower-level building blocks Design, implement, and maintain real-time embedded software using C/C++ for safety-critical medical devices, ensuring compliance with IEC 62304, ISO 13485, ISO 14971, and other relevant medical device standards. Writing and documenting board-level C/C++ code. Lead software architecture and design reviews, ensuring reliability, testability, and scalability Collaborate closely with cross-functional teams, including electrical, mechanical, and systems engineers Drive and perform verification and validation strategies, including unit, integration, and system testing Author and maintain documentation for software architecture, design specifications, and risk analysis Participate in regulatory submissions and support audits when required Maintain traceability between requirements and test protocols, records/reports Follow good laboratory practices to qualify, validate, and maintain tools and equipment Contribute to configuration management and technical/design/milestone reviews Collaborate intensively with Quality, Regulatory, Clinical, and Project Management teams Apply Agile and CI/CD principles to maximize quality and performance About you: Bachelor's or Master's degree in Computer Engineering, Electrical Engineering, or related field Minimum 7 years of experience in embedded software development, preferably in medical device or other regulated industries Strong proficiency in C; working knowledge of C++ and Python is a plus Experience with microcontrollers, RTOS, low-level drivers, and embedded Linux Familiarity with IEC 62304, ISO 13485, and ISO 14971 standards Skilled in hardware abstraction layers, bootloaders, BSP, and driver development Experience with ARM Cortex processors and memory management Proficient in communication protocols (SPI, I2C, UART, CAN, USB) Hands-on debugging using oscilloscopes, logic analyzers, and similar tools Experience with unit testing and test automation frameworks (e.g., CPPUnit, LDRA, Coverity, Parasoft) Familiarity with Agile/Scrum methodologies and tools (e.g., Jira, Azure DevOps) Experience with CI/CD pipelines and build/test infrastructures (e.g., Jenkins, Git, Make, GCC) Strong analytical, documentation, and communication skills Preferred Technical Experience: Knowledge of cybersecurity requirements for connected medical devices (e.g., FDA premarket guidance) Experience with CI/CD pipelines and automated testing in embedded environments 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. Why Join Us? 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 healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success. TPBN1_IJ
Job Description Summary 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 Peripheral Intervention at BD Our Peripheral Intervention (PI) business unit offers a comprehensive range of medical products, devices and services for the treatment of peripheral arterial and venous disease, cancer detection, and end-stage renal disease and maintenance. About the role This role leads the Design Quality team at BD Enniscorthy, with primary responsibility for developing, maintaining, and governing the product risk management file, while providing comprehensive quality engineering support across new product development and product introduction activities. The position ensures full compliance with applicable regulatory requirements and BD procedures, and plays a key role in the planning, development, implementation, and ongoing support of projects, aligning quality objectives with site and organisational goals. Main responsibilities will include: Lead and manage Quality Engineering direct reports, including hiring, performance management, training, development, and corrective actions Ensure compliance with all applicable regulatory requirements, standards, and BD procedures Manage and allocate Quality Engineering resources for New Product Development (NPD) and New Product Introduction (NPI) programs Provide Quality Engineering support for test method validation, product verification and validation, reliability testing, and statistical data analysis Oversee component qualifications, process capability studies, equipment qualifications, and process validations Facilitate and ensure compliance with risk management activities, supporting NPD/NPI teams in generating and maintaining risk files Support field assurance investigations and post-market surveillance activities as required Collaborate closely with R&D and Engineering to enable successful execution of the product development lifecycle and robust product launches Review and approve validation documentation and risk management files; participate in regulatory, corporate, and third-party audits Support regulatory submissions, promote a positive teamwork culture, and contribute to additional projects as assigned About you Required Qualifications Third-level degree in Engineering, Science, or a related technical discipline Minimum of 5+ years' experience in Class II or Class III medical devices, with at least 3 years in a people-management or supervisory role Experience working in a highly regulated environment (medical device, pharmaceutical, or life sciences) Experience & Technical Expertise Strong knowledge of quality and regulatory standards, including QSR, ISO 13485, ISO 14971, MDD/MDR, MDSAP, 21 CFR, and applicable ICH guidelines Hands-on experience with design, process, equipment, test method, and software validation activities Proficiency in Quality Engineering tools such as risk management, root cause analysis, statistics, sampling plans, and process capability studies Experience supporting new product development and commercialization, including risk assessments and component qualification Proven experience conducting and supporting quality and regulatory audits Skills & Competencies Demonstrated ability to drive results, take ownership, and deliver high-quality outcomes in a fast-paced environment Action-oriented mindset with the confidence to make decisions amid complexity and ambiguity Strong customer focus, with the ability to build trusted relationships across internal and external stakeholders Excellent communication, presentation, and influencing skills at all organizational levels Collaborative team leader who promotes engagement, accountability, and continuous learning Strong analytical and problem-solving capabilities, with the ability to effectively prioritize and manage multiple demands Adaptable, self-motivated, and open to innovation and continuous improvement 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. TLNT1_IJ
Job Description Summary We're looking for amazing, passionate and dedicated people to apply their expertise in developing a high-tech, medical device informatics platform. You will need to design, implement, and integrate components across services and devices. You will have to collaborate and communicate effectively with international distributed Agile teams to deliver improvements reliably. You will be expected to contribute to full-stack development, be experienced in the full software development lifecycle, and adhere to a quality management system. 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 Peripheral Intervention at BD Our Peripheral Intervention (PI) business unit offers a comprehensive range of medical products, devices and services for the treatment of peripheral arterial and venous disease, cancer detection, and end-stage renal disease and maintenance. About the role This role is offered on a fixed term contract for a duration of 12 months As a Senior Software Test Engineer, you will play a key role in ensuring the quality and reliability of Software for medical devices. You will work within an agile team environment or independently, driving Software Test Automation and TA frameworks, and supporting both development and sustaining activities. This role requires strong technical expertise, attention to detail, and a proactive approach to continuous improvement. Main responsibilities will include: Collaborate with Product Owners and key stakeholders to estimate work, define milestones, and plan deliverables. Ensure all implementation aligns with business requirements and adheres to agile methodologies. Contribute actively to feature development, code enhancements, and bug resolution. Write clean, efficient, maintainable C# code and promote best engineering practices through example. Lead and maintain architectural consistency across all Clean Architecture layers (Domain, Application, Infrastructure, UI). Ensure adherence to system-wide architectural principles and promote scalable, testable designs. Design and implement features using a Redux-based architecture ( including actions, reducers, effects, and immutable typed state. Build and maintain state-machine-driven workflows (Stateless) supporting long-running operations, retries, timeouts, and error-handling mechanisms within a self-hosted Windows service. Develop and optimize Blazor (Server and/or WebAssembly) components with a focus on performance, lifecycle management, thread-safety, and minimal re-rendering. Implement robust UI patterns, including forms, routing, JS interop, virtualization, and rendering optimization. Maintain comprehensive and up-to-date technical documentation, including architectural diagrams, state diagrams, data contracts, and deployment processes. Communicate effectively with non-technical stakeholders, translating complex technical concepts into clear, understandable language. Provide regular updates on technical risks, progress, and system considerations. Ensure high code quality through automated testing frameworks, including unit tests, reducers/effects tests, and bUnit component tests. Troubleshoot complex issues efficiently and drive continuous improvement across the engineering lifecycle. Stay informed on emerging technologies, frameworks, and industry best practices. Share insights with the team and advocate for appropriate adoption of new tools and methodologies. About you Degree in Computer Science or related field with 5+ years of professional software development experience. Advanced proficiency in C#/.NET, including modern asynchronous programming (async/await, CancellationToken, IAsyncEnumerable, thread-safety patterns). Strong experience designing and implementing Clean Architecture across domain, application, infrastructure, and UI layers. Deep expertise with Blazor (Server and/or WebAssembly), including lifecycle behavior, rendering pipeline, diffing, virtualization, forms, routing, JS interop, and performance tuning. Practical hands-on experience with including actions, reducers, effects, side effects, and associated testing patterns. Experience building complex workflows using Stateless with triggers, guards, retries, timeouts, and deterministic testability. Strong background in ASP.NET Core APIs, background services, streaming endpoints, and device-facing communication protocols (gRPC, SignalR, WebSockets, USB/serial/CAN). Solid understanding of concurrency and thread-safety tools such as SemaphoreSlim, AsyncLock, ReaderWriterLockSlim, lock-free structures, and Blazor UI-thread constraints. Experience developing SPA-style front-end applications. Strong test automation skills using frameworks such as xUnit, NUnit, Moq. Additionally, experience with the following would be a plus: Scrum methodologies and globally-distributed teams .NET Core 8.0 Multi-threaded C# development Offline-first Blazor WebAssembly, background sync Event-sourcing or audit-friendly state persistence Knowledge of JSON and REST based services GIT/Azure DevOps workflow Knowledge of Design Patterns This role is offered on a fixed term contract for a duration of 12 months 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. TPBN1_IJ
We are the people who give possibilities purpose 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. Job Description Our vision for Peripheral Intervention at BD Our Peripheral Intervention (PI) business unit offers a comprehensive range of medical products, devices and services for the treatment of peripheral arterial and venous disease, cancer detection, and end-stage renal disease and maintenance. About the role The Lead Mechanical Design Engineer plays a pivotal role in the design, development, and verification of complex medical devices, encompassing both capital equipment and disposable components. This position demands a multidisciplinary engineering approach, integrating mechanical, mechatronic, electronic, and manufacturing expertise to deliver innovative, high-performance, and compliant solutions. The engineer will be responsible for translating product requirements into detailed specifications, selecting appropriate materials and processes, and conducting feasibility studies and proof-of-concept testing. A key focus will be on driving design and process improvements to enhance product quality, performance, and cost-efficiency, while ensuring manufacturability and scalability. In addition to technical leadership, the role involves managing cross-functional project teams, applying structured project management methodologies, and leading risk assessments such as PHA, FTA, and FMEA. The engineer will oversee root cause analysis and corrective actions, support supplier and subcontractor collaboration, and provide technical guidance throughout the product lifecycle. This role also includes team leadership responsibilities such as recruitment, performance management, and daily coordination of activities to ensure timely execution. The successful candidate will be a strong communicator, capable of leading technical reviews and presentations across internal and external stakeholders, while staying abreast of emerging technologies and tools to continuously elevate engineering capabilities. Main responsibilities will include: Lead and manage the design, development, and verification of complex assemblies, sub-assemblies, components, and packaging. Select appropriate materials, processes, tooling, automation, and equipment to meet design and manufacturing needs. Translate product requirements into comprehensive product specifications. Conduct engineering studies and proof-of-concept testing to evaluate design feasibility. Drive design and process improvements to enhance performance, quality, and cost-efficiency. Lead risk assessments including PHA, FTA, dFMEA/uFMEA for product and manufacturing processes. Perform root cause analysis and implement corrective actions based on failure investigations. Collaborate with manufacturing teams to troubleshoot issues and optimize process parameters. Manage projects or sub-projects, assigning tasks and guiding cross-functional teams. Apply structured project management methodologies and communicate effectively with internal and external stakeholders. Research and integrate emerging technologies and development tools. Oversee recruitment, performance management, and development of direct reports. Coordinate and prioritize daily team activities to ensure timely task completion. Provide technical support to suppliers and subcontract manufacturers. Lead technical reviews and presentations across internal teams and external partners. About you Bachelor's or Master's degree in Mechanical or Biomedical Engineering (or equivalent). 6-9 years of experience in medical device design engineering, including at least 5 years leading mechanical design teams. Proven experience in developing both capital equipment and disposable medical device components. Strong foundation in engineering principles, root cause analysis, and documentation control. Proficient in GD&T and its application in design and inspection. Skilled in Design for Six Sigma (DFFS), statistical analysis, and DOE methodologies. Deep understanding of materials, manufacturing techniques, and design for manufacturability/assembly. Demonstrated leadership with clear ownership of deliverables and team outcomes. Strong analytical reasoning and ability to influence decisions through technical insight. Excellent communication skills and experience managing cross-functional teams. Familiarity with medical device quality and regulatory systems (EN ISO13485, MDR, FDA CFR 820). Knowledge of Stage-Gate or Product Development Life Cycle processes. 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. Why Join Us? 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 healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success. TPBN1_IJ
We are the people who give possibilities purpose 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. 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-centred, 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 (MMS) 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 As a Staff Electrical Engineer, you'll apply your deep understanding of electrical systems, safety standards, and system integration to shape the backbone of our advanced automation platforms. From designing robust electrical architecture to ensuring compliance with EMC and functional safety requirements, your work will be critical to the reliability, scalability, and innovation of our machine and plant systems. You'll take ownership of electrical design and documentation across a diverse range of automation solutions, collaborate closely with interdisciplinary teams, and drive continuous improvement in electrical engineering practices. In a dynamic development environment, you'll have the opportunity to evaluate new technologies, optimise system performance, and contribute to the evolution of next-generation industrial automation. Main responsibilities will include: The position is responsible for the design and development of electro-mechanical systems, components and assemblies for commissioning systems. Contributing to the creation of system architecture Preparation and maintenance of project plans Contribution to and implementation of requirement definitions Creation of electrical schematics and bills of materials, including cabinet and wiring harness designs, as well as drawing creation and modification for harnesses. Selection and specification of electrical components Execution of electro-mechanical calculations and simulations Collaboration with suppliers and contract manufacturers Creation and maintenance of technical documentation (GDP) Initial sample inspections and execution of tests according to test plans About you Bachelor of Eng, in Electrical Engineering or related field, with 10+ years of relevant experience. Outstanding technical capabilities and technical leadership skills T-shaped skill profile: deep expertise in hardware combined with broad knowledge in other areas such as engineering, procurement, quality, and/or manufacturing, ideally across multiple industries Analytical and structured working methodology; self-motivated, organised, with a fact-based and "go-and-see" mentality and a strong drive to understand Experience in System and Reliability Engineering Strong documentation skills (GDP) and practical experience in developing models and graphical representations/abstractions of systems and processes Stakeholder management and networking skills are desirable Experience in common Quality methods (Design Review, DFMEA, Design for Six Sigma, etc.) Solid knowledge of SolidWorks Knowledge of SolidWorks Electrical or EPlan. Regulatory knowledge of the Machinery Directive Knowledge of measurement technology and electromagnetic compatibility (EMC) Excellent MS Office skills (Word, Excel, PowerPoint) Initial experience with MS Project Teammate with strong communication skills Proficiency in English required; German language skills are desirable Familiarity with EN 60204-1 and IEC 61010-1 standards Experience with risk assessment and safety analysis using Safexpert and Sistema Skills in Jira and ERP (Sage) is a plus. 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. TPBN1_IJ
We are the people who give possibilities purpose 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. Job Description Our vision for Peripheral Intervention at BD Our Peripheral Intervention (PI) business unit offers a comprehensive range of medical products, devices and services for the treatment of peripheral arterial and venous disease, cancer detection, and end-stage renal disease and maintenance. About the role As a Staff Systems Engineer, you will contribute to key technical direction and use systems engineering expertise across complex medical device programs. You will play a critical role in defining and/or reviewing existing system architecture, shaping system-level requirements, and driving integration, verification, validation, and risk management activities throughout the product lifecycle. This role requires deep technical expertise combined with the ability to lead through influence, guide cross-functional teams, and navigate ambiguity. You will work closely with engineering, quality, regulatory, clinical, marketing, manufacturing, and service teams to ensure robust, compliant, and customer-focused solutions. Main responsibilities will include: Serve as a key contributor for system architecture, system-level requirements, and interfaces across complex electro-mechanical medical devices. Drive systems engineering excellence across the full product lifecycle, including requirements management, integration, verification, and validation. Author and review system and sub-system requirements, design specifications, and test methods. Significantly contribute to system V&V planning and execution, including protocol development, execution, and reporting. Partner with project management, regulatory, quality, clinical, marketing, and product development teams to drive aligned technical decisions and successful delivery. Apply systems thinking and independent judgment to solve complex technical problems and manage technical risk. Support system and sub-system integration, including defect tracking, configuration management, and interface management. Provide key support to risk management activities, including system-level hazard analysis and FMEA. Plan, design, and analyze technical experiments, including characterization, prototyping, qualification, and design of experiments (DOE). Provide technical mentorship and guidance to junior engineers and systems engineers. Support manufacturability, serviceability, and lifecycle considerations by collaborating with manufacturing and service teams. Apply Design for Six Sigma (DFSS) principles to drive robust design, statistically sound testing, and data-driven decision-making. Develop deep understanding of user needs, clinical workflows, and use environments, ensuring designs meet real-world customer and patient needs. About you Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related engineering discipline. 8+ years of experience in R&D engineering, with significant experience in medical devices, diagnostics, lab automation, or other regulated electro-mechanical systems. Demonstrated expertise in systems engineering principles, including requirements management, architecture development, integration, verification, and validation. Hands-on experience with requirements management tools such as Modern Requirements, Polarion, Jama, or DOORS. Proven experience writing system-level requirements and decomposing them across hardware, software, usability, and mechanical domains. Strong experience developing and executing system-level V&V protocols. Solid knowledge of IEC 60601-1 and relevant medical device standards. Experience working on interdisciplinary systems, including electromechanical, software, and fluidic components. Strong analytical skills, including data acquisition, statistical analysis, and DFSS methodologies. Preferred Qualifications Experience operating effectively in ambiguous, fast-paced, and agile environments, bringing clarity and structure. Demonstrated ability to lead technical complexity and influence decisions without formal authority. Strong communication skills, with the ability to present complex technical concepts clearly to varied audiences. Experience working directly with customers or clinical users to understand workflows, use cases, and unmet needs. Master's degree in Engineering or a related field. This is a 12- Month Fixed Term Contract based in Limerick. Salary Range: €80K - €90K + Bonus + Benefits 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. TPBN1_IJ
We are the people who give possibilities purpose 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. Job Description About the role The Lead Contributor at BD Enniscorthy is responsible for coordinating and monitoring daily manufacturing operations, acting as a key link between production, engineering, maintenance, quality, and supply chain teams to ensure targets are met while upholding high standards of safety, quality, and performance. Reporting to the Senior Manufacturing Unit Leader, the role ensures compliance with GMP and BD procedures and supports the planning, development, and implementation of projects, aligning quality objectives with broader site and organisational goals. Main responsibilities will include: Daily Operations -Contribute to the daily running of manufacturing processes to ensure output meets production schedules. -Support capturing production metrics, and workflow efficiency. -Escalate production issues to engineering/maintenance and support troubleshooting activities. -Ensure work is carried out in accordance with SOPs, GMP, safety policies, and regulatory standards. -Maintaining/tracking manufacturing training matrix & improving the current process. -Responsible for improving/maintaining and monitoring of training within Manufacturing. Process Monitoring & Optimisation -Analyse process data to identify trends. -Recommend and support implementation of process improvements to increase throughput, reduce waste, and improve reliability. -Participate in continuous improvement initiatives such as Lean, Six Sigma, or Kaizen events. Quality & Compliance -Ensure manufacturing activities comply with GMP/ISO and internal quality standards. -Support deviation investigations, NCMR root cause analyses, and corrective/preventive actions (CAPA). -Conduct routine process checks, documentation reviews, and audit readiness tasks. Cross-functional Collaboration & Communication -Work closely with production operators to ensure smooth daily operations and provide process guidance. -Coordinate with quality, engineering, supply chain, and maintenance to address operational needs. -Support new process introductions, equipment commissioning, and validation activities. Documentation & Reporting -Maintain accurate production records, logs, and process documentation. -Prepare daily/weekly operational reports on performance, downtime, and key KPIs. -Ensure timely completion of records and related documentation. Other Responsibilities may include, however are not limited to: Supporting other functions in software validation of equipment controls such as building management systems, facility controls, process equipment controls, HR administrative systems etc Salary Range €36K-40K + Bonus + Benefits This is a 12-month Fixed Term Contract Click on apply if this sounds like you! Why Join Us? 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 healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success. TPBN1_IJ
Job Description Summary The MMS Electronics Engineering Manager leads a growing team of Electronic and Electrical Engineers working across BD's Medication Management and Connected Care platforms, with a primary focus on Infusion Pumps for Acute and Non-Acute applications. 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 is seeking an experienced Electronics Engineering Manager to lead, develop, and grow our team of Electronics Engineers working on advanced electro-mechanical medical devices. This team are involved in driving projects through all phases, from early technology development to full commercialization, while collaborating within a global organization, driving best-practice, and ensuring compliance with industry standards and company objectives. Main responsibilities will include: Lead, mentor, and manage a team of electronic engineers, fostering a collaborative and high-performing environment. Oversee the design, development, and testing of electronic circuits, PCBs, and systems for medical devices, from concept to production. Define technical requirements, specifications, and architecture for electronic components and systems. Conduct design reviews, ensuring adherence to quality standards, regulatory requirements (e.g., IEC 60601), and project timelines. Collaborate with cross-functional teams including mechanical engineering, embedded software engineering, and quality assurance. Manage external vendors and suppliers for electronic components and manufacturing services. Drive continuous improvement initiatives in electronic design processes, tools, and methodologies. Stay abreast of emerging technologies and industry trends in electronics and medical device development. Contribute to project planning, resource allocation, and budget management for electronic engineering activities. Troubleshoot and resolve complex technical issues during development and post-market support. About you: Bachelor's or Master's degree in Electrical Engineering, Electronic Engineering, or a related field. Minimum of 8 years of experience in electronic design and development, with at least 3 years in a leadership or senior technical role. Proven experience in the design of analog and digital circuits, embedded systems, and power management. Proficiency with EDA tools for schematic capture, PCB layout, and simulation (e.g., Altium Designer, OrCAD/Allegro). Strong understanding of signal integrity, EMI/EMC principles, and design for manufacture and assembly (DFM/DFA). Experience with medical device development and regulatory standards (e.g., IEC 60601, ISO 13485) is highly desirable. Excellent problem-solving, analytical, and critical thinking skills. Strong leadership, communication, and interpersonal skills, with the ability to effectively mentor and motivate a team. Ability to work independently and collaboratively in a hybrid work environment. 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. TPBN1_IJ
