Engineer II - Research and Development
Listed on 2026-05-18
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Engineering
Product Engineer, Quality Engineering, Mechanical Engineer
Job Description
Summary: The R&DSustaining Engineering team is seeking a talented and passionate individual to help us be the guardian of product performance, quality, and compliance throughout our products lifecycle. This position will collaborate closely with cross‑functional teams
-R&D, Quality, Regulatory, Marketing, MA and Manufacturing- to troubleshoot issues, implement design changes, and support continuous improvement initiatives. 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.
- Participates in the documentation of sustainability and product development risk activities and design controls
- Applies engineering principles to solve basic engineering problems
- Authors a requirements document for a subsystem or simple component or a section of a requirements document for a larger system
- Reports to manager on progress on tasks that were assigned to them; completes management updates as requested by manager
- Correctly selects and applies analytical methods to interpret small, well‑characterized data sets;
Able to extract key information and its relative importance from data sets;
Able to define conclusions from the data set and present the conclusions logically and in an understandable way for technical individuals - Actively participates in team meetings, makes recommendations, accepts commitments, and delivers commitments
- Interacts with product managers and more experienced engineers to understand the business aspects of product development
- Is a participant and contributes on project teams where technical issues and product development challenges had driven unique solutions
- Bachelor's Degree in S.T.E.M or related field
- 2 to 5+ years of professional experience in product engineering
- Basic understanding of applicable standards and regulations (e.g., FDA 21 CFR 820, ISO 13485, IEC 60601), including design controls, risk management, and documentation.
- Experience developing protocols, test methods, statistical analysis, and test report generation
- Experience gained in a classroom and/or internship or Co‑op setting
- Master’s degree in S.T.E.M
- Experience designing, analyzing, and troubleshooting systems that combine mechanical components, electronics, sensors, and software
- Experience in medical devices or another highly regulated manufacturing environment.
Primary
Work Location:
USA UT - Salt Lake City BAS
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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