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 Job The Design assurance QE is involved in new product development and product sustaining projects through the application of Quality engineering skills. Must be able to handle multiple projects and tasks, from product inception through product launch and maintenance utilizing a high level of written and oral communication skills. Plays 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. Represents the Quality Function on 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 other quality functions as needed for the project. Write project quality plans and support the creation and maintenance of DHF documentation Lead risk management activities within the project. Support the creation and implementation of verification and validation activities Review and approve test protocol and reports. Review and challenge statistical rationale, and data analysis in the frame of test protocol and reports. Review and approve related execution deviations. Assist / conduct Failure investigations and problem-solving sessions Review quality objectives and goals that have been identified and ensure they are sufficiently defined in specifications, procedures, and testing. Conduct quality functional reviews and DHF compliance reviews. Ensure compliance across projects for design control, risk management, and change control processes. Support Quality culture within R&D organisation while providing training on applicable requirements / standards. About you: Completed a level 8 Engineering Degree, in a relevant subject. 3+ years experience within a quality engineering environment. Knowledge in working with ISO 13485, QSR, ISO 14971, statistical techniques. Strong written and verbal communication skills. Strong organisational skills. Experience with IEC 62304 and IEC 62366 - advantage. The Salary Range Information: €55,000 - €65,000 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 Are you ready to make a real impact in healthcare? Join BD, a global leader in medical technology, where your work helps improve lives every day. We're looking for a dedicated and detail-oriented Production Associate to support the hands-on assembly of life-saving medical devices, on a full time permanent basis. Production Associate - Medical Device Manufacturing Location: Enniscorthy, Wexford, Ireland Shift: Days (6.15am to 4.30pm Monday - Thursday) or Evenings (5pm to 3.15am Monday to Thursday) Company: BD - Advancing the World of Health What You'll Do As a Production Associate, you'll play a vital role in our manufacturing operations by: Assembling medical devices with precision and consistency Ensuring compliance with GMP procedures and documentation standards Updating production records and maintaining accurate stock levels Communicating optimally with team members and supervisors Supporting continuous improvement and innovation across the production floor Working with microscopes and minute materials for extended periods Adapting to shift changes and operational needs What We're Looking For Essential Skills: Basic proficiency in Maths and English (written and verbal) Strong attention to detail and dedication to quality Ability to work independently and as part of a team Good communication and timekeeping skills Preferred Skills: Understanding of cleanroom and GMP manufacturing practices Completion of second-level education Basic IT and administrative skills You'll Thrive Here If You... Take personal responsibility and pride in your work Are action-oriented and eager to learn Value teamwork, collaboration, and respectful communication Are passionate about solving customer and patient challenges Embrace innovation and continuous improvement Why Join BD? At BD, we do what's right-not what's easy. We offer: A performance-driven culture that values integrity and accountability Opportunities for growth, learning, and global collaboration A competitive starting rate of €15 per hour and comprehensive benefits package (additional shift rates may also apply) A diverse and inclusive work environment where your voice matters Apply Today Ready to help shape the future of healthcare? Visit BD Ireland Careers to apply and learn more about our commitment to 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 Lead Electronic Engineer directs technical development of all aspects of the electronic and electrical hardware for the the development of BD's Infusion Systems. They provide technical direction for the broader Electronics Engineering team, and collaborate with colleagues across Mechanical Engineering, Systems Engineering, Embedded and Application Software. 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 progressive 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 the Lead Electronic Engineer, you will lead the design, development, and testing of electronic systems and components for innovative medical devices, ensuring compliance with industry standards and company objectives. Main responsibilities will include: Lead the full lifecycle development of electronic hardware, from concept generation and requirements definition to detailed design, prototyping, and validation. Manage and mentor a team of electronic engineers, providing technical guidance, support, and performance feedback. Collaborate cross-functionally with mechanical engineers, software engineers, and quality assurance teams to integrate electronic systems into complex medical devices. Perform circuit design, schematic capture, circuit calculations and simulations, PCB layout review, and component selection. Develop and execute test plans, analyze results, and troubleshoot electronic systems and circuits. Ensure compliance with relevant medical device regulations (e.g., ISO 13485, IEC 60601) and internal quality procedures. Participate in design reviews, risk assessments, and failure mode and effects analysis (FMEA). Stay abreast of new technologies and industry trends in electronics and medical devices. Manage project timelines, budgets, and resources for electronic engineering activities. Prepare technical documentation, including specifications, design descriptions, and test reports. About you: Bachelor's or Master's degree in Electrical Engineering, Electronics Engineering, or a related field. Minimum of 8 years of experience in electronic hardware design and development, with at least 3 years in a senior engineering role. Proven experience in the highly regulated industries (Medical, Military, Aerospace, Automotive) is beneficial but not an absolute requirement. Strong proficiency in analog and digital circuit design, embedded systems, and sensor integration. Expertise with CAD tools for schematic capture and PCB layout (e.g., Altium Designer, OrCAD/Allegro). Experience with microcontrollers, microprocessors, FPGAs, and various communication protocols (e.g., I2C, SPI, UART, USB, Bluetooth). Solid understanding of EMI/EMC principles and design for regulatory compliance. Experience with test equipment (oscilloscopes, spectrum analyzers, logic analyzers). Excellent problem-solving, analytical, and critical thinking skills. Strong leadership, communication, and interpersonal skills. Ability to work independently and as part of a multidisciplinary team. 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. 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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? BD is proud to be certified as a Top Employer 2026 in United Kingdom, reflecting our commitment to creating an exceptional working environment 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 Supply Chain at BD The Supply Chain team are responsible to bringing billions of life-saving medical devices and diagnostics tests, high-tech instruments and equipment to customers and patients all over the world. Our aim is deliver these products at an affordable cost and of the highest quality. About the role As Contract Manufacturing Directoryou will be responsible for the strategic and operational leadership of all outsourced pharmaceutical systems manufacturing activities. The role ensures that Contract Manufacturing Organizations (CMOs) deliver products safely, compliantly, on time, and at the right cost and quality. you will act as the primary interface between the company and CMOs, driving performance excellence, ensuring regulatory compliance, and optimizing the external supply network. Main responsibilities will include: CMO Governance & Performance Management Lead the relationship with assigned CMOs, ensuring strong operational performance and continuous improvement. Establish and oversee governance structures Monitor key metrics Lead issue escalation, resolution pathways, and structured problem-solving with CMO partners. External Manufacturing Strategy Develop and execute the external manufacturing strategy for assigned product portfolio Assess capabilities, risks, and opportunities across the CMO landscape. Contribute to make/buy decisions, outsourcing strategies, and network optimization initiatives. Support business case development for transferring products to new CMOs or scaling capacity. Operational Excellence & Cost Management Drive productivity programs and cost-reduction initiatives across the external network. Ensure robust demand planning, capacity planning, and inventory strategies with CMOs. Review and challenge CMO proposals for cost adjustments, change controls, and capital needs. Negotiate commercial and operational terms in partnership with Procurement. Quality & Compliance Ensure CMOs operate in full compliance with cGMP, ICH, FDA, EMA, and global regulatory standards. Partner with Quality Assurance on audits, inspection readiness, and remediation plans. Oversee change controls, deviation investigations, CAPAs, and risk assessments related to outsourced manufacturing. Support regulatory submissions (CMC sections, responses to HA queries, product variations). Technology Transfer & Lifecycle Management Lead or support technology transfer activities to and from CMOs. Coordinate technical teams for process validation, scale-up, and launch readiness. Drive lifecycle management activities, including formulation changes, process improvements, and cost optimization projects. Ensure robust knowledge transfer and documentation standards during transfers. Cross-Functional Leadership Partner with Supply Chain, Quality, Regulatory, Procurement, R&D, Finance, and Technical Operations to ensure end-to-end performance. Provide leadership to multidisciplinary project teams involving internal and external stakeholders. Act as the internal subject-matter expert for external manufacturing strategy and performance. About you We are looking for an accomplished supply chain leader with a strong track record in managing Contract Manufacturing Organizations (CMOs) across diverse regions and pharmaceutical technologies. The ideal candidate will bring: A minimum of 10 years of experience in the pharmaceutical, medical devices, automotive or consumer goods industry. At least 5 years of direct experience in external/contract manufacturing. Proven leadership in managing CMOs across multiple geographies and technologies, including (but not limited to) sterile manufacturing, oral solid dose, biologics, active pharmaceutical ingredients (API), and packaging. To be successful in this role, you should be able to demonstrate: Strategic Vision: Ability to shape external manufacturing networks and anticipate risks. Technical Depth: Solid grasp of manufacturing technologies, quality, and regulatory standards. Influence & Negotiation: Skilled in leading without authority and managing external partners. Analytical Thinking: Strong problem-solving and data-driven decision-making. Operational Rigor: Proven track record in planning, execution, and performance management. Collaborative Leadership: Effective in matrixed, cross-functional environments. Business Insight: Understanding of cost drivers, contracts, and financial levers. 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. 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Job Description Summary BD is seeking a highly skilled Senior Electronics Engineer to own electronics engineering and product design initiatives for advanced electro-mechanical medical devices. This role involves driving projects through all phases, from early technology development to full commercialisation, while collaborating within a global organisation. As part of a growing team, you will have the opportunity to expand your technical expertise and advance your career in a dynamic and innovative environment. Key responsibilities include designing electronic assemblies and printed circuit boards, ensuring compliance with regulatory standards (UL, IEC, FDA), and conducting EMI, safety, and manufacturability testing. You will work closely with cross-functional teams-mechanical, software, systems, and quality engineering-to align project schedules and budgets. Additional duties include mentoring junior engineers, performing failure analysis, generating design specifications and test documentation, and participating in technical design reviews to guarantee electrical integrity and safety. 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 a highly talented Senior Electronics Engineer to lead electronics engineering and product design. You will be developing electro-mechanical medical devices and supporting projects at all stages, from technology development through commercialisation. As part of an expanding team, you will have excellent opportunities to broaden your knowledge and develop your career within a Global business Main responsibilities will include: Design electronic assemblies and printed circuit board assemblies to support electro-mechanical medical device product development and life cycle. Work with cross functional teams such as mechanical, software, systems and quality engineering to contribute to project schedules and project budgets in the coordination of overall product development. Mentor more junior colleagues. Evaluate and implements designs to ensure that all agency requirements (UL, IEC, FDA) are being met throughout the design process Design and tests for EMI compliance, safety, manufacturability Apply failure analysis skills to determine and document root cause of product system or component failure. Generate design specifications, test protocols and test reports. Participate in technical design reviews to ensure electrical design integrity and safety are achieved. About you Hold a relevant Level 8 degree in Engineering (BSC in Electronics), or equivalent proven experience. 4+ years industry experience in a similar position, Medical Device sector would be a strong advantage. Strong Electronics knowledge, experience with both analog and digital design and mixed signal circuits is required. Experience working in the Medical device Industry, product design experience, EMC testing and experience with requirement documentation are an advantage. Click on apply if this sounds like you! 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. TPBN1_IJ
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. 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
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. TPBN1_IJ
Job Description Summary As the R&D Engineer III, your primary focus of this position will be to support in developing, optimising, implementing, and validating components/elements of a medical device. You will perform hands-on testing in optimisation of a device; conduct process development activities to understand process inputs and outputs; assist/write technical documents, validation protocols and reports; prepare work instructions and standard operating procedures; assist in conducting design and process qualification and validation; support equipment development; support other activities from R&D, Quality, Operations, and Regulatory Affairs. 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: Design: Design components of a medical device, translating intangible design inputs into tangible engineering specifications and drawings. Select appropriate materials, processes and vendors to achieve the design, and challenge these designs against design specifications, clinical use scenarios and international standards. Build test parts for engineering evaluation, pre-clinical studies and clinical studies. Process Development: assists in the development and optimization of processes to understand key process inputs and outputs, using statistic methods such as DOE as appropriate. Supports new process equipment and tooling development, including specification development, vendor selection and negotiation. Documentation: prepare work instructions and standard operating procedures (SOP), write technical documents and reports. Prepare raw material specifications and drawings. Assist in preparing verification and validation protocols and reports. Test Method Development: develop new engineering test methods and clinically relevant simulated use test methods in conjunction with R&D technicians; prepare and assist in the validation of test methods. Testing: perform lab bench testing, conduct engineering and competitor evaluations, development unit testing, and execute verification and validation activities. Training: train technicians on new design and process development as well as new test methods. Assist/conduct new process development training with operations and quality assurance. Supervisory/mentoring/coaching: Mentor/coach R&D technicians through New Product Development activities like new process development, R&D materials/inventory control etc. May lead or manage technicians or engineering interns. Other Responsibilities may include, however are not limited to: Assist in the support of Manufacturing, Quality, Regulatory & R&D to ensure systems are compliant with all internal and external guidelines. Assist in design and process root cause analysis and support non-conforming product and complaint investigations. About you: B.S. degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or other related engineering discipline. Biomedical Engineering or Bioengineering degree preferred. Up to 4 years of industrial experience in R&D or process development, preferably in medical device or other regulated FDA/QSR and ISO environment. Demonstrated hands-on technical aptitude. Experience in process validation (IQ, OQ and PQ), writing protocols and reports to support verification and validation activities for product commercialization; ability to assist in executing validation. Excellent oral and written communication skills. Ability to work in cross functional teams. Ability to analyze data, interpret results, and write reports. Proficient in statistic software is a distinct advantage. Knowledge of cGMP and GLP is a distinct advantage. Training in Six Sigma or Design for Six Sigma is a distinct advantage. 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
Job Description Summary The Lead Electronic Engineer directs technical development of all aspects of the electronic and electrical hardware for the the development of BD's Infusion Systems. They provide technical direction for the broader Electronics Engineering team, and collaborate with colleagues across Mechanical Engineering, Systems Engineering, Embedded and Application Software. 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 progressive 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 the Lead Electronic Engineer, you will lead the design, development, and testing of electronic systems and components for innovative medical devices, ensuring compliance with industry standards and company objectives. Main responsibilities will include: Lead the full lifecycle development of electronic hardware, from concept generation and requirements definition to detailed design, prototyping, and validation. Manage and mentor a team of electronic engineers, providing technical guidance, support, and performance feedback. Collaborate cross-functionally with mechanical engineers, software engineers, and quality assurance teams to integrate electronic systems into complex medical devices. Perform circuit design, schematic capture, circuit calculations and simulations, PCB layout review, and component selection. Develop and execute test plans, analyze results, and troubleshoot electronic systems and circuits. Ensure compliance with relevant medical device regulations (e.g., ISO 13485, IEC 60601) and internal quality procedures. Participate in design reviews, risk assessments, and failure mode and effects analysis (FMEA). Stay abreast of new technologies and industry trends in electronics and medical devices. Manage project timelines, budgets, and resources for electronic engineering activities. Prepare technical documentation, including specifications, design descriptions, and test reports. About you: Bachelor's or Master's degree in Electrical Engineering, Electronics Engineering, or a related field. Minimum of 8 years of experience in electronic hardware design and development, with at least 3 years in a senior engineering role. Proven experience in the highly regulated industries (Medical, Military, Aerospace, Automotive) is beneficial but not an absolute requirement. Strong proficiency in analog and digital circuit design, embedded systems, and sensor integration. Expertise with CAD tools for schematic capture and PCB layout (e.g., Altium Designer, OrCAD/Allegro). Experience with microcontrollers, microprocessors, FPGAs, and various communication protocols (e.g., I2C, SPI, UART, USB, Bluetooth). Solid understanding of EMI/EMC principles and design for regulatory compliance. Experience with test equipment (oscilloscopes, spectrum analyzers, logic analyzers). Excellent problem-solving, analytical, and critical thinking skills. Strong leadership, communication, and interpersonal skills. Ability to work independently and as part of a multidisciplinary team. 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. 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