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BD
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  • Quality Engineer - Design Assurance  

    - Limerick

    Overview 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. 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 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. Salary Range €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. To learn more about BD visit: https://bd.com/careers 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. To learn more about BD visit https://bd.com/careers. 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. Required Skills Optional Skills Primary Work Location IRL Limerick - Castletroy Additional Locations Work Shift At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You." Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed. Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role. Salary Range Information €43,300.00 - €66,025.00 EUR Annual #J-18808-Ljbffr

  • BD is seeking a Senior Scientist in Limerick, Ireland, to lead the development of advanced flow cytometry solutions. You will be responsible for designing experiments and driving innovative product strategies while collaborating with cross-functional teams. The role requires at least a Master's degree or PhD in Immunology or a related field, along with 3 years of industry experience. A competitive salary range of €56,600 - €86,300 EUR annually is offered, reflecting the expertise in flow cytometry and leadership skills required. #J-18808-Ljbffr

  • Senior Scientist Immunology  

    - Limerick

    About the role Serving as a Senior Scientist, you will be instrumental in building the next generation of flow cytometry solutions. You will lead the invention of innovative products that advance our reagent portfolio. Acting as a technical leader and trusted expert, you will develop and implement complex experimental strategies involving reagent systems, assays, workflows, and instruments. You will translate complex data into clear insights that drive product decisions. In close collaboration with cross‑functional product development and clinical trial teams, you will ensure solutions uphold technical excellence, customer needs, and regulatory guidelines as applicable. This opportunity allows you to apply independent judgement, critical thinking, and deep scientific expertise to solve complex problems, influence system‑level requirements, and present influential findings to internal teams and external scientific audiences—all while mentoring junior scientists and encouraging a culture of scientific rigor and innovation. Main Responsibilities Lead experimental studies in the laboratory and participate in cross‑functional discussions to support the program's goals. Demonstrate knowledge of customer workflows, scientific, and technological advancements. Effectively communicate technical concepts, project plans, and test strategies that balance risk and business objectives; support budget planning based on functional project scope. Lead analysis and presentations of moderate to high complexity at technical reviews. Direct and supervise teams or mentor junior team members. Act as a technical contributor on cross‑functional core teams, assist decision‑making across functions, and offer input to senior management on strategic and functional decisions. About You MSc or PhD or equivalent experience in Immunology, Cell Biology, Clinical Laboratory Science, or related scientific field with a minimum of 3 years of relevant industry experience. Experience in Flow Cytometry and customer workflows. Proven ability to research and apply scientific principles to develop new or improve existing processes with a focus on hematology, immunology, and/or molecular genetics. Skill in accomplishing complex experiments independently, performing analysis, interpreting experimental results, making sound conclusions, and performing statistical analysis. Creative problem‑solving skills for novel or complex applications. Critical evaluation of proposed study builds with knowledge of statistics, calculation of sample sizes, and/or estimation of statistical power. Experience in researching and applying scientific principles to build new or optimise existing laboratory procedures. Ability to train bench‑level personnel at multiple levels of education and/or expertise. Strong interpersonal skills with a proven ability to engage effectively with others in multi‑disciplinary team settings, guide decision‑making, and develop group consensus. Excellent written and oral communication skills. Preferred Qualifications / Capabilities PhD or equivalent experience and post‑doctoral experience in Immunology/Immuno‑oncology with expertise in immunophenotypic analysis of human tissue samples by flow cytometry. Experience in leading small to medium‑sized teams of technical contributors. 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. Salary Range Information: €56,600.00 - €86,300.00 EUR Annual #J-18808-Ljbffr

  • Senior Immunology Scientist: Flow Cytometry Leader  

    - Limerick

    BD is looking for a Senior Scientist in Limerick, Ireland, to play a key role in developing flow cytometry solutions. This position involves leading innovative projects, collaborating with various teams, and applying deep scientific knowledge to complex problems. Candidates should have a MSc or PhD with at least 3 years of experience in related fields, alongside strong skills in flow cytometry, critical thinking, and communication. The role also includes mentoring junior scientists and addressing customer workflows. A competitive salary range of €56,600 to €86,300 EUR annually is offered. #J-18808-Ljbffr

  • Lead Electronics Engineer  

    - Limerick

    Job Description Summary The Lead Electronic Engineer directs technical development of all aspects of the electronic and electrical hardware for 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 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. Primary Work Location IRL Limerick - Castletroy Equal Opportunity Employer 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. Salary Range Information 73,500.00 - 112,125.00 EUR Annual #J-18808-Ljbffr

  • 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 Responsibilities Set the global strategic direction for your spend category in collaboration with business and procurement leaders within our Hub & Spoke model. Develop and deploy Category Sourcing Strategies across the organization, ensuring alignment with Business Units and R&D. Analyze market trends, cost drivers, and global risks to build forward‑looking sourcing strategies. Handle end‑to‑end procurement activities, including supplier evaluations, site audits, and continuous improvement initiatives. Build and maintain a high‑performing supplier base capable of meeting current and future business needs. Lead complex, enterprise‑wide negotiations and develop robust contracts in partnership with Legal. Drive supplier performance through structured business reviews focused on cost, quality, and delivery. Champion compliance and ethical standards, ensuring alignment with company values and governance. Promote continuous improvement using Lean Six Sigma tools to elevate procurement processes and outcomes. Qualifications and Experience Bachelor’s degree and 8+ years of experience in industrial direct material procurement (in manufacturing or healthcare). Deep proficiency in strategic sourcing methodologies, including the five‑step approach. Confirmed negotiation skills and ability to build a pipeline of cost‑saving opportunities in a worldwide scale. Analytical approach with the ability to assess market trends and supplier capabilities. Excellent communication skills in English (additional languages are a plus). Proactive, results‑oriented approach with a track record of successful strategy execution. Compensation range for this position: 170 000 to 190 000 CHF per year. This position is located in the Canton of Vaud, Switzerland. Applicants must hold a valid Swiss work permit and be legally resident in the Canton of Vaud. Equal Opportunity Employer 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, affectionate or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics. #J-18808-Ljbffr

  • Global Category Leader – Plastic Components  

    - Cork

    BD is looking for a procurement professional to lead strategic sourcing efforts. The successful candidate will have over 8 years of experience in industrial direct material procurement, focusing on the healthcare sector. This role involves collaborating with business leaders, analyzing market trends, and driving supplier performance. A Bachelor's degree is required, and the position is based in County Cork, Ireland with a competitive salary range of 170,000 to 190,000 CHF annually. #J-18808-Ljbffr

  • Senior Electronics Engineer  

    - Limerick

    Job Description Summary BD is seeking a highly skilled Senior Electrical Engineer to own electrical 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 commercialization, while collaborating within a global organization. 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 Design electronic assemblies and printed circuit boards, ensuring compliance with regulatory standards (UL, IEC, FDA), and conducting EMI, safety, and manufacturability testing. Work closely with cross‑functional teams—mechanical, software, systems, and quality engineering—to align project schedules and budgets. Mentor junior engineers, perform failure analysis, generate design specifications and test documentation, and participate in technical design reviews to guarantee electrical integrity and safety. Job Description 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. 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 looking for a highly talented Senior Electrical Engineer who will be responsible for leading electrical engineering and product design. You will be developing electro‑mechanical medical devices and supporting projects in all phases, from technology development through commercialization. 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! Primary Work Location IRL Limerick - Castletroy Salary Range Information €54,800.00 - €83,600.00 EUR Annual Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. To learn more about BD visit: https://jobs.bd.com/ At BD, we are strongly committed to investing in our associates—their well‑being and development, and in providing rewards and recognition opportunities that promote a performance‑based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You. Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates’ progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location. #J-18808-Ljbffr

  • Design Quality Lead — Medical Devices (NPD/NPI)  

    - Enniscorthy

    A leading medical device company in Enniscorthy is seeking a Quality Engineering Lead to manage the Design Quality team. The role involves ensuring compliance with regulatory requirements and providing support for product development. Candidates should have a third-level degree in Engineering or Science, with over 5 years of experience in medical devices and at least 3 years in a supervisory role. The estimated salary ranges from €54,800 to €83,600 annually, with flexible work arrangements offered. #J-18808-Ljbffr

  • Design Quality Lead  

    - Enniscorthy

    About The Role This role leads the Design Quality team at BD Enniscorthy, with primary responsibility for developing, maintaining, and governing the product risk management file, while providing comprehensive quality engineering support across new product development and product introduction activities. The position ensures full compliance with applicable regulatory requirements and BD procedures, and plays a key role in the planning, development, implementation, and ongoing support of projects, aligning quality objectives with site and organisational goals. Main Responsibilities Lead and manage Quality Engineering direct reports, including hiring, performance management, training, development, and corrective actions Ensure compliance with all applicable regulatory requirements, standards, and BD procedures Manage and allocate Quality Engineering resources for New Product Development (NPD) and New Product Introduction (NPI) programs Provide Quality Engineering support for test method validation, product verification and validation, reliability testing, and statistical data analysis Oversee component qualifications, process capability studies, equipment qualifications, and process validations Facilitate and ensure compliance with risk management activities, supporting NPD/NPI teams in generating and maintaining risk files Support field assurance investigations and post‑market surveillance activities as required Collaborate closely with R&D and Engineering to enable successful execution of the product development lifecycle and robust product launches Review and approve validation documentation and risk management files; participate in regulatory, corporate, and third‑party audits Support regulatory submissions, promote a positive teamwork culture, and contribute to additional projects as assigned About You Required Qualifications Third‑level degree in Engineering, Science, or a related technical discipline Minimum of 5+ years’ experience in Class II or Class III medical devices, with at least 3 years in a people‑management or supervisory role Experience working in a highly regulated environment (medical device, pharmaceutical, or life sciences) Experience & Technical Expertise Strong knowledge of quality and regulatory standards, including QSR, ISO 13485, ISO 14971, MDD/MDR, MDSAP, 21 CFR, and applicable ICH guidelines Hands‑on experience with design, process, equipment, test method, and software validation activities Proficiency in Quality Engineering tools such as risk management, root cause analysis, statistics, sampling plans, and process capability studies Experience supporting new product development and commercialization, including risk assessments and component qualification Proven experience conducting and supporting quality and regulatory audits Skills & Competencies Demonstrated ability to drive results, take ownership, and deliver high‑quality outcomes in a fast‑paced environment Action‑oriented mindset with the confidence to make decisions amid complexity and ambiguity Strong customer focus, with the ability to build trusted relationships across internal and external stakeholders Excellent communication, presentation, and influencing skills at all organizational levels Collaborative team leader who promotes engagement, accountability, and continuous learning Strong analytical and problem‑solving capabilities, with the ability to effectively prioritize and manage multiple demands Adaptable, self‑motivated, and open to innovation and continuous improvement Location Primary Work Location: IRL Wexford - Enniscorthy Work Arrangement Most roles require a minimum of 4 days of in-office presence per week to maintain culture of excellence and smooth operations, while offering flexibility for work‑life balance. Compensation & Benefits Salary Range: €54,800.00 – €83,600.00 EUR Annual Equal Opportunity 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. #J-18808-Ljbffr

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