Job DescriptionThe R&D team is seeking an exceptionally talented and passionate individual to help us 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 in this position 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 a strong capability to interpret and ensure
compliance with all local, state, federal and BD safety regulations, quality policies, best practices, and
procedures through appropriate communication.
This position is responsible for technical leadership and domain expertise in the area of pediatric and neonatal catheter development. This position is of a technical rather than managerial nature. Individuals in this position will typically lead a technical group and may manage major projects in more than one technical area. In addition, this position may provide technical expertise to other groups or projects.
Job Responsibilities: (Primary Duties, Roles, and/or Authorities)- Leads effort to determine new product development efforts and priorities.
- Consultant/Division expert; Division Technical expert.
- Provides technical leadership and domain expertise to cross-functional project teams aimed at the development of medical devices.
- Works closely with other functions (i.e., Marketing, Operations, Quality, Engineering R&D) to troubleshoot, characterize and resolve needs in existing and adjacent devices.
- Develops Innovative ideas for the organization.
- Participates and leads cross-functional teams.
- Provides technical support on components, material methods, systems, and equipment.
- Critical Decision Maker in areas of engineering and business needs.
- Prepares procedures, author technical reports, publishes research papers, and makes recommendations based on their research findings.
- Engages in collaborative efforts with academics, hospitals, and other external organizations.
- May have responsibility for managing third-party relationships.
- Develops and/or directs experimentation.
- Effective communication skills to be able to translate technology and science into the business and position this to drive strategic decisions for the future (including strong presentation skills before large audiences).
- Has experience and successful track record of understanding clinical needs and translating that information into successful products.
- Responsible for concept generation, design, development and evaluation of new products, materials, and technologies.
- Mentors and trains less experienced colleagues in best practices for product development, technology development, clinical assessment, manufacturing, and process development.
- Manages project planning, budgeting, scheduling, and tracking.
- Plans and coordinates engineering test builds.
Education and Experience:Minimum Qualifications:- A bachelor's degree in STEM (Science, Technology, Engineering, Math), and ten (10) years of engineering experience within a regulated industry, including at least two (2) years of experience in the medical device industry, Or:
- Or a master's degree in STEM and eight (8) years of engineering experience within a regulated industry, including at least two (2) years of experience in the medical device industry.
Preferred Qualifications:- Experience in the medical device industry strongly preferred.
Knowledge and Skills:Essential Knowledge and Qualification Skills:- Excellent analytical skills & discipline; able to conduct thorough analysis of concepts that have high uncertainty.
- Excellent critical thinking skills; able to constructively challenge ideas and invite critical feedback.
- Demonstrated familiarity with FDA, ISO, and Good Manufacturing Practice guidelines and regulatory compliance.
- Strong knowledge of scientific, engineering, and technical principles.
- Advanced engineering skills/specialized technical expertise:
o Molding/Extrusion.
o Design/mechanics/FEA.
o Statistics/Design of Experiments.
o Biocompatibility/coatings/materials.
o Clinical trials and animal testing.
Preferred Accomplishments related to technical expertise:
o National Committee/Association Leadership.
- Able to draw upon technical breadth to evaluate concepts outside area(s) of personal expertise.
- Proven ability to foster a collaborative team environment.
- Excellent written and oral communications skills
- Ability to concurrently handle various projects and coordinate cross-functional teams' efforts.
- Ability to work with in-house and outside support groups.
- Ability to independently work with outside medical and technical professionals.
- Strong skills in communicating with all levels of technical and operating management.
- Strong ability to analyze and use technical data and resources.
- Oral and written comprehension; Inductive and deductive reasoning.
- Broad business and technical knowledge.
- Influences others across organization.
Desired Knowledge and Qualification Skills:- Strong interpersonal and influencing skills.
- Excellent technical judgment.
- Effective communication skills.
- Demonstrated accountability for successful completion of designated tasks.
- Team-oriented.
- Understanding of disciplined product development processes and quality requirements.
- Understanding and ability to design for high volume manufacturing and/or durable electro/mechanical medical devices.
- Strong fit with BD values.
- Experience with specific tools and methods, such as: statistical tools and Design of Experiments (DOE), computer analysis and engineering fundamentals to support sound engineering judgment.
- Solidworks, Minitab, and FEA (Abaqus / Fluent) experience is preferred.
- Knowledge of regulatory and quality requirements (21CFR820.30).
- Understanding of failure theory and modes for plastics, elastomers, and metals due to static and time-variable loading conditions.
- 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, particularly those of plastic injection molding, metal stamping and automated assembly techniques, including solvent bonding, adhesive bonding, ultrasonic welding, and interference-fitting.
- Experience with manufacturing process validation including strategy development, First Article Inspection, and Factory Acceptance Testing.
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.
For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Required Skills
Optional Skills
Primary Work LocationUSA UT - Sandy
Additional LocationsWork Shift 
