Milpitas, Santa Clara County, CATodayFull-timeOn-site
Job • The Associate Director of Engineering is the senior engineering leader at the site level, responsible for engineering execution, technical governance, and performance.
Job • The Associate Director of Engineering is the senior engineering leader at the site level, responsible for engineering execution, technical governance, and performance.
Key Accountabilities This position is accountable for working across all ISC Engineering functions to horizontally align appropriate levels of technical talent to projects while interfacing with Business Units and other functional leaders to ensure project delivery excellence.
Key Accountabilities This position is accountable for working across all ISC Engineering functions to horizontally align appropriate levels of technical talent to projects while interfacing with Business Units and other functional leaders to ensure project delivery excellence.
Minimum Education Bachelor's degree required in Engineering, Mechanical Engineering preferred. Minimum Experience Two years medical manufacturing experience preferred.
Minimum Education Bachelor's degree required in Engineering, Mechanical Engineering preferred. Minimum Experience Two years medical manufacturing experience preferred.
You'll have the opportunity to grow our Safety and Sustainability Culture, influencing the mindset of associates, peers, and even leadership in meaningful, uplifting ways Required Qualifications Bachelor of Science degree in Environmental Engineering, Environment Health and Safety, Occupational Health and Safety, Mechanical Engineering, Electrical Engineering, Process Engineering, or equivalent, preferred.
On-site
in critical areas like Machine Guarding, Lock Out Tag Out (LOTO), and other essential safety programs
Drive Sustainability: Stay connected to site Sustainability targets and projects, ensuring we achieve our environmental goals and make a positive impact
Champion Certification: Be a core contributor to our ISO 14001 certification efforts
You'll have the opportunity to grow our Safety and Sustainability Culture, influencing the mindset of associates, peers, and even leadership in meaningful, uplifting ways Required Qualifications Bachelor of Science degree in Environmental Engineering, Environment Health and Safety, Occupational Health and Safety, Mechanical Engineering, Electrical Engineering, Process Engineering, or equivalent, preferred.
On-site
in critical areas like Machine Guarding, Lock Out Tag Out (LOTO), and other essential safety programs
Drive Sustainability: Stay connected to site Sustainability targets and projects, ensuring we achieve our environmental goals and make a positive impact
Champion Certification: Be a core contributor to our ISO 14001 certification efforts
Job • ESSENTIAL FUNCTIONS The essential functions of this position include but are not limited to Acts as a resource to work groups and project teams, within the plant and outside the plant relative to quality and regulatory issues. • Leads or participates on Kaizen teams to improve quality and reduce waste.
Job • ESSENTIAL FUNCTIONS The essential functions of this position include but are not limited to Acts as a resource to work groups and project teams, within the plant and outside the plant relative to quality and regulatory issues. • Leads or participates on Kaizen teams to improve quality and reduce waste.
Job Job Responsibilities Responsibilities include but are not limited to • Process Optimization & Manufacturing • Provide day-to-day engineering support to pharmaceutical manufacturing operations.
Job Job Responsibilities Responsibilities include but are not limited to • Process Optimization & Manufacturing • Provide day-to-day engineering support to pharmaceutical manufacturing operations.
Job Job Responsibilities Responsibilities include but are not limited to • Process Optimization & Manufacturing • Provide day-to-day engineering support to pharmaceutical manufacturing operations.
Job Job Responsibilities Responsibilities include but are not limited to • Process Optimization & Manufacturing • Provide day-to-day engineering support to pharmaceutical manufacturing operations.
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.
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 • 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 • 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.
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.