About the position
BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. The Urology and Critical Care (UCC) division focuses on developing innovative solutions that improve patient outcomes and enhance the quality of care. As an Engineer in the R&D department, you will be an integral part of a cross-functional team focused on the design, development, and testing of medical devices. This role is ideal for recent graduates or early-career professionals eager to grow their engineering skills in a collaborative and mission-driven environment. You will work under the guidance of senior engineers and project leaders, contributing to product development from concept through commercialization. In addition to new product development, this role also supports Sustaining Engineering initiatives to ensure the continued performance, compliance, and improvement of existing medical devices.
Responsibilities
- Support the design and development of medical devices in accordance with BD’s product development process and regulatory requirements.
- Assist in creating and executing test protocols, analyzing data, and documenting results.
- Participate in design reviews, brainstorming sessions, and risk assessments.
- Collaborate with cross-functional teams including Quality, Regulatory, Manufacturing, and Marketing.
- Develop CAD models, engineering drawings, and prototypes using tools such as SolidWorks.
- Maintain accurate and organized documentation in compliance with design control procedures.
- Contribute to continuous improvement initiatives and support root cause investigations.
- Collaborate on Sustaining Engineering activities, including product updates, compliance reviews, and support for manufacturing and field issues.
Requirements
- Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related field.
- 0–2 years of relevant engineering experience (internships/co-ops included).
- Familiarity with engineering design principles, materials, and manufacturing processes.
- Basic understanding of FDA regulations and ISO standards for medical devices is a plus.
- Proficiency in CAD software (e.g., SolidWorks) and Microsoft Office Suite.
- Strong analytical, problem-solving, and communication skills.
- Eagerness to learn, grow, and contribute in a team-oriented environment.
Nice-to-haves
- Internship or co-op experience in a regulated industry (medical device, pharma, etc.).
- Exposure to design controls, risk management, and verification/validation activities.
- Experience with lab equipment and testing methodologies.
Benefits
- On-site collaboration to foster creativity and innovation.
- Flexibility and work-life balance.
- Opportunities for learning and growth.
