EXPERIENCE • A minimum of 12 years engineering experience. • Preferred background is in automated manufacturing equipment, with process development in high volume manufacturing. • Experience with medical devices, in-vitro diagnostic and pharmaceutical products are a plus. • Experience implementing process improvements and launching new equipment into a manufacturing environment.
EXPERIENCE • A minimum of 12 years engineering experience. • Preferred background is in automated manufacturing equipment, with process development in high volume manufacturing. • Experience with medical devices, in-vitro diagnostic and pharmaceutical products are a plus. • Experience implementing process improvements and launching new equipment into a manufacturing environment.
Quality Engineer role will apply knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and quality systems/procedures to optimize product development, internal and external device manufacturing, and device distribution.
Quality Engineer role will apply knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and quality systems/procedures to optimize product development, internal and external device manufacturing, and device distribution.
Education and • Experience Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or a related technical field with 4 + years of relevant experience , or Master’s degree in Engineering or related field with 2+ years of relevant experience What You’ll • Work On Products across BD’s UCC platforms, including endourology, urinary incontinence, and urinary management Minimally invasive and catheter-based devices across urology and critical care applications External partner-developed technologies integrated into BD’s portfolio • Design changes, risk reduction, and product lifecycle improvements Emerging and next-generation technologies across UCC platforms • Design improvements and new product development Key Responsibilities • Lead engineering workstreams for evaluation, integration, and modification of medical devices Independently assess external partner designs for technical soundness, risk, and compliance • Define and drive test strategies, validation plans, and data-driven decision making • Ensure rigorous application of design controls and risk management (ISO 14971, FDA QSR) Serve as a technical lead interface with external partners and suppliers, influencing decisions and challenging assumptions • Collaborate with Marketing to translate user needs and emerging market trends into engineering requirements • Mentor junior engineers and contribute to development of team technical capability • Drive high-quality engineering documentation (DHF, reports, risk files) suitable for regulatory submission Technical Skills (Expected Level of Competence) Working Knowledge (expected) Design controls and regulatory frameworks (ISO 13485, 21 CFR 820.30) Risk management (ISO 14971) Test method development, validation, and data interpretation Technical evaluation of developed and in-development products and data Statistical analysis and interpretation of engineering data Supplier/manufacturing processes impacting product quality Product development lifecycle documentation (DHF, protocols, reports) Exposure (preferred) • Intellectual property, FTO considerations, and competitive landscape • Experience in endourology or minimally invasive device development , including ureteroscopes, catheters, access systems, or fluid management Understanding of urinary tract anatomy and physiology (kidneys, ureters, bladder) • Experience with clinical workflow of endourological procedures Demonstrated success working with external development partners or OEMs • Experience translating clinical/user insights into product requirements • Familiarity with urology market trends and technologies Location Covington, GA (On-site 4 days/week) 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.
Education and • Experience Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or a related technical field with 4 + years of relevant experience , or Master’s degree in Engineering or related field with 2+ years of relevant experience What You’ll • Work On Products across BD’s UCC platforms, including endourology, urinary incontinence, and urinary management Minimally invasive and catheter-based devices across urology and critical care applications External partner-developed technologies integrated into BD’s portfolio • Design changes, risk reduction, and product lifecycle improvements Emerging and next-generation technologies across UCC platforms • Design improvements and new product development Key Responsibilities • Lead engineering workstreams for evaluation, integration, and modification of medical devices Independently assess external partner designs for technical soundness, risk, and compliance • Define and drive test strategies, validation plans, and data-driven decision making • Ensure rigorous application of design controls and risk management (ISO 14971, FDA QSR) Serve as a technical lead interface with external partners and suppliers, influencing decisions and challenging assumptions • Collaborate with Marketing to translate user needs and emerging market trends into engineering requirements • Mentor junior engineers and contribute to development of team technical capability • Drive high-quality engineering documentation (DHF, reports, risk files) suitable for regulatory submission Technical Skills (Expected Level of Competence) Working Knowledge (expected) Design controls and regulatory frameworks (ISO 13485, 21 CFR 820.30) Risk management (ISO 14971) Test method development, validation, and data interpretation Technical evaluation of developed and in-development products and data Statistical analysis and interpretation of engineering data Supplier/manufacturing processes impacting product quality Product development lifecycle documentation (DHF, protocols, reports) Exposure (preferred) • Intellectual property, FTO considerations, and competitive landscape • Experience in endourology or minimally invasive device development , including ureteroscopes, catheters, access systems, or fluid management Understanding of urinary tract anatomy and physiology (kidneys, ureters, bladder) • Experience with clinical workflow of endourological procedures Demonstrated success working with external development partners or OEMs • Experience translating clinical/user insights into product requirements • Familiarity with urology market trends and technologies Location Covington, GA (On-site 4 days/week) 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.
Key Responsibilities New Product Development & Industrialization • Lead DFMA strategy for new products and product design changes to ensure successful commercialization and transfer to manufacturing. • Partner with R&D during product development to influence design decisions that improve manufacturability, assembly, quality, and cost. • Define and develop scalable manufacturing processes, equipment concepts, and assembly methods for new product introductions. • Lead engineering efforts to build pilot lines and establish capable, efficient manufacturing processes that achieve performance, quality, and OEE targets. • Support internal and external manufacturing transfer activities, including industrialization planning and factory readiness.
Key Responsibilities New Product Development & Industrialization • Lead DFMA strategy for new products and product design changes to ensure successful commercialization and transfer to manufacturing. • Partner with R&D during product development to influence design decisions that improve manufacturability, assembly, quality, and cost. • Define and develop scalable manufacturing processes, equipment concepts, and assembly methods for new product introductions. • Lead engineering efforts to build pilot lines and establish capable, efficient manufacturing processes that achieve performance, quality, and OEE targets. • Support internal and external manufacturing transfer activities, including industrialization planning and factory readiness.
Job • The Senior Engineer, New Product Introduction (NPI) will lead and drive the successful transition of new medical device products from design and development into commercial manufacturing.
Job • The Senior Engineer, New Product Introduction (NPI) will lead and drive the successful transition of new medical device products from design and development into commercial manufacturing.
Job Responsibilities • include but are not limited to • Lead in the identification and ensure implementation of opportunities to optimize/improve manufacturing processes including using engineering methods (e.g., SIX Sigma and LEAN methods) employing technical design skills to re-design/design of and ensure equipment, tools, fixtures, etc. are up to standards • Drive the development and manage the execution of complex experiments and tests (including writing and executing protocols) on a simple product line to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports • Collaborate with first & second-tier suppliers on process development and process validation including IQ/OQ/PQ/TMVs.
Job Responsibilities • include but are not limited to • Lead in the identification and ensure implementation of opportunities to optimize/improve manufacturing processes including using engineering methods (e.g., SIX Sigma and LEAN methods) employing technical design skills to re-design/design of and ensure equipment, tools, fixtures, etc. are up to standards • Drive the development and manage the execution of complex experiments and tests (including writing and executing protocols) on a simple product line to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports • Collaborate with first & second-tier suppliers on process development and process validation including IQ/OQ/PQ/TMVs.
Job Responsibilities • include but are not limited to • Lead in the identification and ensure implementation of opportunities to optimize/improve manufacturing processes including using engineering methods (e.g., SIX Sigma and LEAN methods) employing technical design skills to re-design/design of and ensure equipment, tools, fixtures, etc. are up to standards • Drive the development and execution of experiments and tests (including writing and executing protocols) on a simple product line to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports • Collaborate with first & second-tier suppliers on process development and process validation including IQ/OQ/PQ/TMVs.
Job Responsibilities • include but are not limited to • Lead in the identification and ensure implementation of opportunities to optimize/improve manufacturing processes including using engineering methods (e.g., SIX Sigma and LEAN methods) employing technical design skills to re-design/design of and ensure equipment, tools, fixtures, etc. are up to standards • Drive the development and execution of experiments and tests (including writing and executing protocols) on a simple product line to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports • Collaborate with first & second-tier suppliers on process development and process validation including IQ/OQ/PQ/TMVs.
Job POSITON SUMMARY The Automation Servicer Engineer (ASE) is responsible for attending to service needs of BD Advanced Diagnostics customers within their assigned geographic territory, as well as nationally, on an as-needed basis, utilizing appropriate tools and test equipment and schematic diagrams.
Job POSITON SUMMARY The Automation Servicer Engineer (ASE) is responsible for attending to service needs of BD Advanced Diagnostics customers within their assigned geographic territory, as well as nationally, on an as-needed basis, utilizing appropriate tools and test equipment and schematic diagrams.
Job POSITON SUMMARY The Automation Servicer Engineer (ASE) is responsible for attending to service needs of BD Advanced Diagnostics customers within their assigned geographic territory, as well as nationally, on an as-needed basis, utilizing appropriate tools and test equipment and schematic diagrams.
Job POSITON SUMMARY The Automation Servicer Engineer (ASE) is responsible for attending to service needs of BD Advanced Diagnostics customers within their assigned geographic territory, as well as nationally, on an as-needed basis, utilizing appropriate tools and test equipment and schematic diagrams.
Job • Summary As an Associate Principal Engineer, the chosen candidate will serve as the Platform Technology • Architect for the Pump & Fluid Platform across the UCC urine evacuation product portfolio.
Job • Summary As an Associate Principal Engineer, the chosen candidate will serve as the Platform Technology • Architect for the Pump & Fluid Platform across the UCC urine evacuation product portfolio.
Job • We are seeking a highly experienced Senior Staff AI/ML Algorithm Engineer to help advance next-generation medical technologies for continuous physiological monitoring, disease detection, and predictive clinical decision support.
Job • We are seeking a highly experienced Senior Staff AI/ML Algorithm Engineer to help advance next-generation medical technologies for continuous physiological monitoring, disease detection, and predictive clinical decision support.
The successful candidate will bring hands-on experience as a Quality Engineer supporting product development, along with a demonstrated ability to improve and scale quality processes.
The successful candidate will bring hands-on experience as a Quality Engineer supporting product development, along with a demonstrated ability to improve and scale quality processes.
Job • The Team The Applied ML/AI Algorithms team leads the development of advanced algorithms that power BD Advanced Patient Monitoring’s next generation of clinically impactful products.
Job • The Team The Applied ML/AI Algorithms team leads the development of advanced algorithms that power BD Advanced Patient Monitoring’s next generation of clinically impactful products.
Job • Manufacturing Engineer We are looking for a motivated Manufacturing Engineer to support high-speed automated filling operations for medical diagnostic reagents.
Job • Manufacturing Engineer We are looking for a motivated Manufacturing Engineer to support high-speed automated filling operations for medical diagnostic reagents.
Job Summary As part of the Systems Engineering group, the Systems Engineer II will play a key role in supporting the BD portfolio of products that involve electromechanical hemodynamic monitoring equipment.
Job Summary As part of the Systems Engineering group, the Systems Engineer II will play a key role in supporting the BD portfolio of products that involve electromechanical hemodynamic monitoring equipment.
Milpitas, Santa Clara County, CATodayFull-timeOn-site
The Senior Staff Engineer is responsible for the definition and management of requirements, definition of product architecture, guiding characterization of prototype systems, and successful Verification and Validation.
The Senior Staff Engineer is responsible for the definition and management of requirements, definition of product architecture, guiding characterization of prototype systems, and successful Verification and Validation.
Job • The Packaging Engineer is responsible for the design, development, validation, implementation, and continuous improvement of packaging systems for medical devices manufactured at the site.
On-site
on packaging-related projects and change controls.
Education & Experience
Bachelor’s degree in Packaging Engineering, Mechanical Engineering, Industrial Engineering, Manufacturing Engineering, Biomedical Engineering, or related technical field.
Job • The Packaging Engineer is responsible for the design, development, validation, implementation, and continuous improvement of packaging systems for medical devices manufactured at the site.
On-site
on packaging-related projects and change controls.
Education & Experience
Bachelor’s degree in Packaging Engineering, Mechanical Engineering, Industrial Engineering, Manufacturing Engineering, Biomedical Engineering, or related technical field.
Engineering • Support - Resolve minor manufacturing assembly and test issues to support instrument and sub-assembly production; also perform testing, validations, and designs of experiments under the guidance of the department staff.
Engineering • Support - Resolve minor manufacturing assembly and test issues to support instrument and sub-assembly production; also perform testing, validations, and designs of experiments under the guidance of the department staff.