Job Description Summary The Lead Mechanical Design Engineer is responsible for leading the design, development, and verification of complex medical devices, including both capital equipment and disposable components. This role requires a multidisciplinary approach, applying expertise in mechanical, mechatronic, electronic, and manufacturing engineering to deliver innovative and compliant solutions. Key responsibilities include preparing product specifications, developing assembly and testing strategies, and ensuring robust, manufacturable designs. The role also involves systematic analysis of technical data to understand device functionality and resolve root cause failures. 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 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. High attention to detail and a quality-first mindset with proven documentation skills. 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.
Job Description Summary Join our team as an In-House Clinical Research Associate / Supply Specialist, where you will play a key role in supporting clinical studies through careful management of study products and supplies. You will collaborate with multiple teams across different sites to ensure all materials are available, compliant, and properly documented. This role requires precision, organisation, and strong interpersonal skills to support smooth study execution from start-up to close-out. OUR VISION FOR BDB AT BD BD Biosciences (BDB) is a leading provider of high-quality flow cytometry and single-cell genomics solutions, scientific research and clinical laboratories. Here, we are leading the way by developing the best technologies that have the ability to look closer at the details of cells and diseases. 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! Main responsibilities will include: Monitor and maintain inventory of study reagents, laboratory supplies, and study products across multiple sites. Inspect study products, including packaging and labelling, ensuring compliance with standard operating procedures. Assist in kit assembly, label formatting, over-labelling, and packaging design to support study execution and protocol adherence. Support packaging and shipping of materials, both domestically and internationally, following IATA regulations where applicable. Maintain accurate study documentation, including Clinical Trial Master File (TMF) creation and updates, study logs, and reports. Work with study site teams to provide necessary documents for ethics submissions, site start-up, and ongoing study activities. Assist with audits, internal and external, including preparation, reconciliation, and archival of study materials. Support project and team activities, including meeting preparation, minutes, and other assigned projects. About you: Hold a BA/BS in Science, Engineering, Pharmacy, or related healthcare or life sciences field. Possess at least 2 years of relevant clinical operations experience. Demonstrate strong organisational skills and attention to detail. Collaborate effectively within multidisciplinary teams in a matrix environment. Communicate clearly and professionally with internal and external partners. Show initiative, creativity, and the ability to manage multiple tasks simultaneously. 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. 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.
Job Description Summary The Senior Software Test Engineer in BD's Diagnostic Solutions (DS) team will help deliver a cutting-edge middleware platform that connects medical devices with hospital systems, supporting advanced diagnostic capabilities. This role combines hands-on technical work with collaboration across geographically distributed teams, requiring strong communication skills, a proactive approach to problem-solving, and a commitment to continuous improvement and innovation in healthcare technology. 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 Diagnostic Solutions at BD BD Diagnostic Solutions is a division of BD (Becton, Dickinson and Company), a global medical technology leader dedicated to advancing the world of health. The Diagnostic Solutions business focuses on enabling accurate, timely and efficient detection of infectious diseases, cancer and other health conditions. Through innovations in microbiology, molecular diagnostics and point-of-care devices and assays, BD Diagnostic Solutions supports customers around the world, whether in high-throughput laboratories or community healthcare clinics, in hospitals or at-home, in delivering better outcomes for patients. About the role As a Senior Software Test Engineer at BD, you will play a critical role in advancing our vision of streamlining and innovating diagnostic technologies with a strong focus on customer experience and product quality. You will join a dynamic Agile team focused on developing a robust middleware platform that bridges medical devices with hospital Laboratory Information Systems (LIS). Main Responsabilities: Collaborate with project teams (local and remote) to understand requirements, estimate, plan, design and deliver the product under test. Understand design, and implementation level details of the product under test. Learn the automation framework and add test scripts Create, execute and review test cases and other test documents as per Design and Change controls Conduct complex black box, system-level, functional testing, applying comprehensive knowledge of software quality concepts within the software development lifecycle, verify end-to-end customer flows, Capture Issue/Bugs in line with Business Unit policy/Standard and track to closure Perform sprint and V&V test execution tasks Guide, lead other testers in the team complying with the R&D Quality Management System Contribute to technical decision making Support software and systems engineering teams with troubleshooting, characterization and validation activities for prototypes, sub-systems, and finished products. Engage in continuous improvement of test process, innovation and optimize test processes. Apply comprehensive knowledge of software quality concepts within the software development lifecycle. About you: Bachelor's/Master's degree in Computer Science, Engineering or related discipline, plus a minimum of 6 years of software testing experience Minimum of 2 years experience in automation tools such as - Selenium, Cucumber, TestComplete. Good knowledge of programming languages - preferably C# Experience testing web applications or product testing with knowledge on API and DB testing, perform API validations and be able to create SQL script Experience with Defect Tracking Tools, Requirement Management and Test Management Tools such as TFS, ADO, HP OpenText ALM, Cognition Cockpit Generate and analyze Test related metrics using the data from the defect management systems Experience with Agile and Scrum methodologies in software development Excellent interpersonal skills, decision-making, and problem-solving skills Demonstrated ability to learn, introduce and improve new and existing test practice and process Effectiveness of understanding and communicating technical information and ability to translate information between technical and business languages Experience with complete software product development life cycle from concept to final release is expected Effective written and verbal communications skills, ability to clearly and precisely communicate with management and remote team members Nice to have: Familiarity with FDA regulations for medical instruments, ISO 13485, IEC 62304 standards and Quality Management systems Experience working in the regulated medical industry ISTQB or equivalent certificate in Software Testing or Software Automation Testing. 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.
Job Description Summary The Software Engineer in BD's Integrated Diagnostic Solutions (IDS) team, you will help build / Maintain a middleware platform that connects medical devices with hospital systems, supporting advanced diagnostic capabilities. Working in an Agile environment, you'll contribute across the full software development lifecycle-designing, coding, testing, and maintaining applications using technologies like C#, ASP.NET, WPF and SQL Server. This role combines hands-on technical work with collaboration across geographically distributed teams, requiring strong communication skills, a proactive approach to problem-solving, and a commitment to continuous improvement and innovation in healthcare technology. 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 Integrated Diagnostic Solutions at BD By aligning and simplifying our work, our Integrated Diagnostic Solutions (IDS) business unit aims to drive growth and innovation around everything from integrated specimen management to diagnostic solutions. About the role As a Software Engineer at BD, you will play a critical role in advancing our vision of streamlining and innovating diagnostic technologies. You will join a dynamic Agile team focused on developing / maintaining a robust middleware platform that bridges medical devices with hospital Laboratory Information Systems (LIS). This high-impact role requires strong expertise in development using C#, ASP.NET, WPF, as well as a solid understanding of the software development lifecycle. Your contributions will support the delivery of diagnostic solutions that improve patient outcomes and healthcare efficiency. In this role, you'll work closely with Product Owners and partners to estimate, plan, and deliver key tasks throughout the project timeline. You will lead by example in writing clean, maintainable code and mentoring peers through complex technical challenges. From creating architectural designs and maintaining technical documentation to exploring emerging technologies, your work will drive continuous improvement and innovation. This role also requires effective communication with multi-functional teams and non-technical collaborators, ensuring transparency and clarity throughout the development process. Main responsibilities will include: Collaborate with Product Owners and partners to determine estimation and define project achievements, work, and timelines. Actively contribute to coding and development tasks. Address complex technical challenges and effectively resolve issues. Keep all user documentation current and detailed. Stay abreast of the latest trends and advancements in software development and share that learning with the team. Explore and adopt new technologies and methodologies where applicable. Communicate effectively with non-technical collaborators, translating complex technical concepts into understandable terms. Provide regular updates on project progress and technical issues. About you Strong technical expertise and a minimum of 3 - 5+ years of experience in C#, ASP.NET, WPF and .NET Framework. Experience with Microsoft SQL Server. Applicants should possess experience in writing unit/integration tests and developing applications using a development approach that priorities testing. Experience with source control systems such as Azure DevOps and Git. Ability to perform, implement and support higher and lower environments across a multi-layered team spanning multiple geographical locations Must have excellent interpersonal skills, decision-making, and problem-solving skills. 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.
Job Description Summary As the Staff R&D Systems Engineer, you will contribute to cross-disciplinary product development teams and may lead the definition, design, and execution of Systems Engineering activities throughout all phases of the product lifecycle. 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 We're looking for a Staff R&D Engineer with a strong systems mindset to lead the development and evolution of complex medical technologies. In this role, you'll play a pivotal part in shaping product architecture, defining system-level requirements, and driving integration and verification activities across the product lifecycle-from concept through commercialization and post-market support. You'll collaborate across multidisciplinary teams to ensure our solutions meet user needs, regulatory standards, and performance expectations. Whether you're passionate about systems thinking, product architecture, or hands-on experimentation, this role offers the opportunity to make a meaningful impact on innovative healthcare solutions. Key Responsibilities Lead systems-level design and development activities for both new and existing products. Define and maintain system and product architectures, ensuring alignment with user needs and business goals. Translate user and stakeholder needs into clear, actionable system requirements and interface definitions. Drive traceability from requirements through design, implementation, and verification. Lead system integration efforts, including defect tracking, configuration management, and risk analysis. Plan and execute system-level testing, analyze data, and communicate findings through reports and design reviews. Support verification and validation activities, including protocol development and execution. Collaborate with Manufacturing, Quality, and Reliability teams to ensure smooth product transitions and resolve field issues. Facilitate cross-functional technical reviews and contribute to risk management activities (e.g., dFMEA, hazard analysis). Apply creative problem-solving and critical thinking to resolve complex technical challenges. About You Proven experience in R&D for complex electro-mechanical systems-medical devices, diagnostics, lab automation, or similar. Strong foundation in systems engineering principles, including requirements management, architecture development, integration, and verification. Skilled in experimental design, data analysis, and drawing insights from test results. Comfortable navigating ambiguity and driving clarity in fast-paced, agile environments. Effective communicator and collaborator with the ability to influence across functions and lead without formal authority. Demonstrated ability to manage technical complexity and deliver results in cross-functional project teams. Self-motivated, curious, and eager to learn new technologies and approaches. Click on apply if this sounds like you! 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/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.
Job Description Summary The Senior Software Engineer in BD's Integrated Diagnostic Solutions (IDS) team, you will help build a cutting-edge middleware platform that connects medical devices with hospital systems, supporting advanced diagnostic capabilities. Working in an Agile environment, you'll contribute across the full software development lifecycle-designing, coding, testing, and maintaining applications using technologies like C#, ASP.NET Core, Angular, and SQL Server. This role combines hands-on technical work with collaboration across geographically distributed teams, requiring strong communication skills, a proactive approach to problem-solving, and a commitment to continuous improvement and innovation in healthcare technology. 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 Integrated Diagnostic Solutions at BD By aligning and simplifying our work, our Integrated Diagnostic Solutions (IDS) business unit aims to drive growth and innovation around everything from integrated specimen management to diagnostic solutions. About the role As a Senior Software Engineer at BD, you will play a critical role in advancing our vision of streamlining and innovating diagnostic technologies. You will join a dynamic Agile team focused on developing a robust middleware platform that bridges medical devices with hospital Laboratory Information Systems (LIS). This high-impact role requires strong expertise in full-stack development using C#, ASP.NET Core, and Angular, as well as a solid understanding of the software development lifecycle. Your contributions will support the delivery of brand-new diagnostic solutions that improve patient outcomes and healthcare efficiency. In this role, you'll work closely with Product Owners and partners to estimate, plan, and deliver key tasks throughout the project timeline. You will lead by example in writing clean, maintainable code and mentoring peers through complex technical challenges. From creating architectural designs and maintaining technical documentation to exploring emerging technologies, your work will drive continuous improvement and innovation. This role also requires effective communication with multi-functional teams and non-technical collaborators, ensuring transparency and clarity throughout the development process. Main responsibilities will include: Collaborate with Product Owners and partners to determine estimation and define project achievements, work, and timelines. Ensure the team correctly implements and follows agile methodologies. Actively contribute to coding and development tasks. Lead by example in writing clean, efficient, and maintainable code. Address complex technical challenges and effectively resolve issues. Foster a culture of innovation and continuous improvement. Keep all user documentation current and detailed, covering architectural designs, API documentation, and deployment procedures. Stay abreast of the latest trends and advancements in software development and share that learning with the team. Explore and adopt new technologies and methodologies where applicable. Communicate effectively with non-technical collaborators, translating complex technical concepts into understandable terms. Provide regular updates on project progress and technical issues. About you Strong technical expertise and a minimum of 5 - 7 + years of experience in C# and .NET Framework Strong JavaScript framework expertise and confirmed experience in Angular Entity Framework, XML querying, T-SQL Experience with Microsoft SQL Server 5+ years confirmed experience with Typescript, RxJS, HTML, LESS/CSS and Node.js, .NET Core Applicants should possess experience in writing unit/integration tests and developing applications using a development approach that prioritises testing Experience with source control systems such as Azure DevOps and Git Proven understanding of, and experience with SOA and RESTful architectures Ability to perform, implement and support higher and lower environments across a multi-layered team spanning multiple geographical locations Must have excellent interpersonal skills, decision-making, and problem-solving skills Exposure to Agile and SAFe methodology 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.
Job Description Summary As a Design Assurance Quality Engineer (QE), you will play a key role in ensuring that new product development and sustaining projects meet stringent quality and compliance standards. Acting as the Quality representative on project core teams, you will oversee design controls, risk management, and change control processes while driving adherence to global regulatory requirements. Your responsibilities will span from product inception through launch and maintenance, requiring strong collaboration with cross-functional teams and effective communication skills. You will lead risk management activities, manage Design History File (DHF) documentation, and support compliance initiatives such as IEC 60601 and IEC 62304. The role involves reviewing and approving verification and validation plans, challenging statistical rationales, and authorizing deviations. You will also assist in failure investigations, software issue tracking, and advocate for a strong quality culture across projects. Additionally, you will contribute to broader Quality Management System (QMS) activities, including CAPA, field assessments, and operational engineering evaluations. 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 As Build Assurance QE, you will be involved in new product development and product sustaining projects through the application of Quality Engineering skills. You will balance multiple projects and tasks, from product inception through product launch and maintenance utilising a high level of written and oral communication skills. You will play an active role in the processes to ensure products meet quality and compliance standards consistent with both Corporate and global standards and regulations while meeting all design controls, risk management, change control requirements, and other applicable regulatory requirements. The Design Assurance QE represents the Quality Function on the Project core teams for both new product development and existing products. Main responsibilities will include: Be the Design Assurance Quality Engineer on project core teams for design change projects and develop close relationships with core team members and extended quality functions as needed for the project. Contribute to the formation and ongoing management of DHF documentation Lead risk management activities within the project. Drive compliance management activities (e.g., IEC 60601) on the project with support from the Compliance Engineer. Demonstrate a patient-first approach to quality engineering. Support the creation and implementation of verification and validation activities. Work closely with R&D functions to ensure comprehensive testing of product requirements and the execution of the V&V plan. Review and approve testing procedures and documentation. Review and challenge the statistical rationale and data analysis within the test protocol and reports. Assess and authorise related execution deviations. Assist/conduct Failure investigations and problem-solving sessions. Responsible for the software issue tracking process per IEC 62304 to ensure software issues are logged, risk assessed and dispositioned appropriately. Ensure compliance across projects for design control, risk management, and change control processes. Advocate for a strong quality culture within project core teams Support of other QMS activities outside of projects, such as CAPA, Field Assessment and operations engineering assessments. About you A relevant degree or equivalent experience (engineering degree preferred), or a minimum of 5 years of quality engineering experience as an equivalent qualification Knowledge in working with ISO 13485, QSR, ISO 14971, and statistical techniques Expertise in design assurance, including design controls, standards compliance, and risk management Strong written and verbal communication skills Strong organisational skills Experience with MDR - advantage Experience with IEC 62304 and IEC 62366 - advantage Ability to influence. Assess the situation and determine if a blocking issue is triggered. 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.
Job Description Summary As the Senior Financial Accountant, you will manage US GAAP month-end and year-end close for Research Centre Ireland, overseeing General Ledger processes, and ensuring accurate reporting and compliance. Some of the key responsibilities will include R&D Tax Credit and IDA grant submissions, audit coordination, and collaboration with internal finance teams and external stakeholders. You will also support budgeting cycles, statutory accounts, tax calculations, and intercompany processes, playing a vital role in maintaining financial integrity across multiple entities. 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! Main responsibilities will include: Actively contribute as an engaged member of the local finance team and the wider GBS RTR finance group, supporting business objectives. Manage US GAAP month-end and year-end close reporting for Research Centre Ireland, including cost centre analysis and balance sheet reconciliations. Oversee all aspects of General Ledger processing and validation, including transaction processing, review, and reconciliation. Calculate and submit the annual R&D Tax Credit Claim, working closely with R&D stakeholders and the wider R&D group. Manage annual IDA claim submissions and drawdowns for BD RCI, including audit management of claims and liaison with external auditors and IDA. Collaborate on annual and quarterly budget and projection cycles specifically related to R&D tax credits and IDA grant estimations. Ensure accurate submissions to Revenue Commissioners for expense reporting, small benefits, and share schemes. Support external audit processes for BD Ireland legal entities preparation of statutory accounts and tax calculations, ensuring timely completion. Liaise with external auditors, tax advisors, Revenue Commissioners, and other regulatory bodies to maintain statutory and regulatory compliance. Work closely with BD's wider finance teams, including Consolidations, Treasury, Intercompany, and shared service providers. Partner with Tax and intercompany teams on transfer pricing calculations and processes. About you: Qualified accountant (ACA, ACCA, CPA, or CIMA) with +5 years PQE - ideally in a multinational environment Strong technical accounting knowledge (IFRS + US GAAP) Proven experience working with ERP systems (e.g., SAP, Oracle, JDE) for financial reporting and analysis Excellent analytical skills and proficiency in Excel (Power BI an advantage) This positon is offered on a 2 year FTC basis. 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.
Job Description Summary We are looking for a highly motivated and experienced Senior Firmware Engineer to join our global R&D team in developing embedded software for optoelectronic and electromechanical devices used in consumer, industrial, and medical applications. In this role, you will be responsible for designing, implementing, and documenting board-level C/C++ firmware, contributing across the full software development lifecycle while adhering to quality and regulatory standards. You will collaborate with cross-functional teams through the entire product lifecycle-from concept development to commercialization and post-market support-to deliver high-performance, reliable, and scalable firmware solutions. You will also drive and support integration, testing, and troubleshooting activities. This is a unique opportunity to influence the development of life-changing healthcare solutions in a regulated and fast-paced environment. 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 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 High-energy, self-motivated, and able to work effectively in a diverse, international team 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. 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.
Job Description Summary We are looking for a Manufacturing Process Engineer, for our facility in BD Enniscorthy. You will assist with all process engineering activities relating to the day to day support of the Manufacturing Unit and you will perform tasks associated with these activities including the key areas of process support and process troubleshooting. You will be responsible for assisting in the development, implementation, and continuous improvement of processes to produce products that meet customer requirements and are cost-effective. You will report to Manufacturing Process Engineering Lead or Senior Manufacturing Unit Leader. 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, end-stage renal disease and maintenance. Main responsibilities will include: Improve product quality, labor efficiency, and throughput through the use improved manufacturing techniques using Six Sigma principles. Participate and sometimes leads on project teams with engineers, technicians and other professionals of various disciplines/departments to continuously improve product, equipment, and fixture processes on the manufacturing area Initiate and develop process validations, software validation and equipment validations Identify and Update revision of SOP's to reflect current practice Perform engineering work typically including one of the following: process/product improvements, test of materials, preparation of specifications, process study, evaluation of process models/process improvements, development improvement of equipment, tools, fixtures and report preparation Understands and performs Project plans, risk analysis project updates and Project implementation for more complex projects Understands and can create Process FMEA (Failure Mode Effects Analysis) review and update Update of manufacturing and test method Documentation to reflect current practice Part of a team that can conduct complaints investigations, CAPA investigations and Continuous Improvement activities to improve the product or process. Plans and coordinates engineering test builds. Participates in analysis of problems in design, process and test development, using Six Sigma principles. Prepares and presents oral and written project updates and technical discussions. Basic understanding of EHS standards and requirements with regard to process / equipment design and operation and follows all EHS standard on site including but not limited to LOTO, Guarding, Contractor management, Equipment Design standards, Chemical handling and chemical safety. Supporting other functions in software validation of equipment controls such as building management systems, facility controls, process equipment controls, HR administrative systems etc About you: Minimum of bachelor's degree in engineering or a related topic. Several years of experience within a regulated manufacturing setting. Ability to make and present engineering decisions, with excellent problem solving ability. Strong interpersonal skills, with the ability to work with cross functional teams. Excellent knowlegde of tooling, design and drafting. Expereince analysing and optimising existing processes and ability to create new processes. Familiar with creating, analysing and optimising manufacturing and quality systems. Ability to create and provide training where needed. Expereince with reviewing and coordinating test protocols and reports Ability to generate engineering proposals. Six Sigma Knowledge, Yellow Belt Certified. 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.
