BD
Overview
The R&D team is seeking an exceptionally talented and passionate individual to help identify and implement innovative solutions to address current and future health care needs in the Vascular Access markets. Within BD Medication Delivery Solutions (MDS) Research & Development, the associate will be part of the Salt Lake City R&D team. Our R&D Engineers are responsible for developing and implementing new product designs, product improvements, and critical component changes for disposable and durable medical devices. The preferred candidate will have strong technical design skills, excellent written and oral skills, and leadership abilities. This candidate should possess the ability to interpret and ensure compliance with local, state, federal and BD safety regulations, quality policies, best practices, and procedures through appropriate communication. This position assists the R&D Engineering Teams in designing, developing, and implementing new products, processes, test methods and equipment. 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. 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 believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a
maker of possible
with us. Responsibilities
Lead cross-functional design control activities Consultant/Department expert with technical expertise and business knowledge Organizational credibility and knowledge Guide and direct others within the Department while being results oriented and a project Leader Initiate new or revised documentation and track through appropriate approval cycles and implementation Participate and/or lead cross-functional teams Provide technical support on components, material methods, systems, and equipment Develop physical and functional test requirements to assure specifications and regulations are met Write and approve protocols, reports, and data Oversee testing outlined in protocols and test methods Coordinate/develop validation studies on equipment and processes Execute design controls and analyze design inputs Conduct complaint investigations Understand and follow company procedures and regulatory requirements Prepare and submit approval requests for project funding; participate in project planning, budgeting, scheduling, and tracking Plan and coordinate engineering test builds Analyze problems in design, process, and test development; recommend solutions Prepare and present oral and written project updates and technical discussions Mentor and provide technical guidance to junior engineers and team members The duties and responsibilities are representative and not all-inclusive Essential Knowledge And Qualification Skills
Ability to make and present engineering decisions Ability to manage multiple projects from initiation through closing phases Determine and communicate project deliverables Develop a work breakdown structure, estimates, and viable schedule Execute and control projects through closure Specialized engineering skills: cost analysis, basic tooling design and drafting, process optimization, manufacturing and quality systems, prototyping Ability to train and critique training; strong interpersonal skills Apply comparative statistics Software application skills Problem solving ability Create, review and coordinate test protocols and reports Generate engineering proposals Oral and written presentation skills Lead cross-functional teams Create and execute project plans Budget creation and control Desired Knowledge And Qualification Skills
Strong interpersonal and influencing skills Excellent technical judgment Effective communication skills Material science Bioengineering principles Accountability for completing designated tasks Team-oriented Understanding of disciplined product development processes and quality requirements Strong alignment with BD values Applying statistical tools, computer analysis and engineering fundamentals; Solidworks, Minitab, and FEA experience preferred Design of Experiments (DOE) Knowledge of regulatory and quality requirements (21CFR820.30) Understanding of failure theory and modes for plastics, elastomers, and metals under static and time-variable loading Experience with clinical studies, human physiology, and simulated product use studies Experience with contact and non-contact metrology Knowledge of high-volume manufacturing and assembly processes (plastic injection molding, metal stamping, automated assembly, solvent/adhesive bonding, ultrasonic welding, interference-fitting) Experience with manufacturing process validation (FAI, FAT) Required Qualifications
A bachelor’s degree in STEM (preferably mechanical or Biomed) and four 4–6 years of engineering experience in medical devices or a regulated industry Or a master’s degree in STEM and two 2 years of engineering experience in medical devices or a regulated industry 4–6 years of experience with design, development, production, and validation of devices creating mechanical systems and models Experience in medical device or equivalent regulated industry Travel: 10% Schedule: 4 days onsite (Mon–Thu), 1 day remote (Friday) Location: Salt Lake City, Utah Preferred Qualifications
Master’s degree in STEM Physical Demands
This position is in an office and laboratory environment and may require sitting, standing, lifting up to 25 pounds occasionally, and occasional bending, stooping, and reaching Work Environment and Vaccination
BD prioritizes on-site collaboration to foster creativity and problem-solving. A minimum of 4 days in-office per week is typical for many roles. Remote or field-based roles will have different arrangements stated in the job posting. Some roles require proof of full vaccination against COVID-19; testing may be available or required in some locations, with accommodations considered per BD policy. Why Join Us?
A career at BD means being part of a team that values your opinions, helps you grow, holds each other accountable, and learns and improves daily. We seek people who can see the bigger picture and help reinvent the future of health. You’ll find a culture where you can learn, grow, and thrive. To learn more about BD, visit https://bd.com/careers 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.
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The R&D team is seeking an exceptionally talented and passionate individual to help identify and implement innovative solutions to address current and future health care needs in the Vascular Access markets. Within BD Medication Delivery Solutions (MDS) Research & Development, the associate will be part of the Salt Lake City R&D team. Our R&D Engineers are responsible for developing and implementing new product designs, product improvements, and critical component changes for disposable and durable medical devices. The preferred candidate will have strong technical design skills, excellent written and oral skills, and leadership abilities. This candidate should possess the ability to interpret and ensure compliance with local, state, federal and BD safety regulations, quality policies, best practices, and procedures through appropriate communication. This position assists the R&D Engineering Teams in designing, developing, and implementing new products, processes, test methods and equipment. 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. 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 believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a
maker of possible
with us. Responsibilities
Lead cross-functional design control activities Consultant/Department expert with technical expertise and business knowledge Organizational credibility and knowledge Guide and direct others within the Department while being results oriented and a project Leader Initiate new or revised documentation and track through appropriate approval cycles and implementation Participate and/or lead cross-functional teams Provide technical support on components, material methods, systems, and equipment Develop physical and functional test requirements to assure specifications and regulations are met Write and approve protocols, reports, and data Oversee testing outlined in protocols and test methods Coordinate/develop validation studies on equipment and processes Execute design controls and analyze design inputs Conduct complaint investigations Understand and follow company procedures and regulatory requirements Prepare and submit approval requests for project funding; participate in project planning, budgeting, scheduling, and tracking Plan and coordinate engineering test builds Analyze problems in design, process, and test development; recommend solutions Prepare and present oral and written project updates and technical discussions Mentor and provide technical guidance to junior engineers and team members The duties and responsibilities are representative and not all-inclusive Essential Knowledge And Qualification Skills
Ability to make and present engineering decisions Ability to manage multiple projects from initiation through closing phases Determine and communicate project deliverables Develop a work breakdown structure, estimates, and viable schedule Execute and control projects through closure Specialized engineering skills: cost analysis, basic tooling design and drafting, process optimization, manufacturing and quality systems, prototyping Ability to train and critique training; strong interpersonal skills Apply comparative statistics Software application skills Problem solving ability Create, review and coordinate test protocols and reports Generate engineering proposals Oral and written presentation skills Lead cross-functional teams Create and execute project plans Budget creation and control Desired Knowledge And Qualification Skills
Strong interpersonal and influencing skills Excellent technical judgment Effective communication skills Material science Bioengineering principles Accountability for completing designated tasks Team-oriented Understanding of disciplined product development processes and quality requirements Strong alignment with BD values Applying statistical tools, computer analysis and engineering fundamentals; Solidworks, Minitab, and FEA experience preferred Design of Experiments (DOE) Knowledge of regulatory and quality requirements (21CFR820.30) Understanding of failure theory and modes for plastics, elastomers, and metals under static and time-variable loading Experience with clinical studies, human physiology, and simulated product use studies Experience with contact and non-contact metrology Knowledge of high-volume manufacturing and assembly processes (plastic injection molding, metal stamping, automated assembly, solvent/adhesive bonding, ultrasonic welding, interference-fitting) Experience with manufacturing process validation (FAI, FAT) Required Qualifications
A bachelor’s degree in STEM (preferably mechanical or Biomed) and four 4–6 years of engineering experience in medical devices or a regulated industry Or a master’s degree in STEM and two 2 years of engineering experience in medical devices or a regulated industry 4–6 years of experience with design, development, production, and validation of devices creating mechanical systems and models Experience in medical device or equivalent regulated industry Travel: 10% Schedule: 4 days onsite (Mon–Thu), 1 day remote (Friday) Location: Salt Lake City, Utah Preferred Qualifications
Master’s degree in STEM Physical Demands
This position is in an office and laboratory environment and may require sitting, standing, lifting up to 25 pounds occasionally, and occasional bending, stooping, and reaching Work Environment and Vaccination
BD prioritizes on-site collaboration to foster creativity and problem-solving. A minimum of 4 days in-office per week is typical for many roles. Remote or field-based roles will have different arrangements stated in the job posting. Some roles require proof of full vaccination against COVID-19; testing may be available or required in some locations, with accommodations considered per BD policy. Why Join Us?
A career at BD means being part of a team that values your opinions, helps you grow, holds each other accountable, and learns and improves daily. We seek people who can see the bigger picture and help reinvent the future of health. You’ll find a culture where you can learn, grow, and thrive. To learn more about BD, visit https://bd.com/careers 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.
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