Principal Systems Engineer, R&D - BD Advanced Patient Monitoring

Principal Systems Engineer, R&D - BD Advanced Patient Monitoring

BD (Tissuemed Ltd)
• Work on advanced hemodynamic monitoring solutions.

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

• Write and execute Design Verification Protocols while effectively organizing, capturing, and analyzing test results.
• Plan, collect, and translate detailed information about user interactions with critical care medical devices and connectivity solutions through interviews, field observation, task analysis, simulation labs.
• Support system requirements development and management related to device connectivity, usability, user experience, and testing.
• Provide technical support to Regional Marketing and Sales teams for pre‑sale efforts.
• Support communication with hospital IT departments for initial deployment questions, setup, and testing strategy.
• Work with sales, marketing, and quality/complaint handling teams for post‑market surveillance.
• Drive technical root cause investigations, engaging appropriate R&D, quality, and vendor resources.
• Identify and create new product features and collaborate with Software development team through clear communication, wireframes, and storyboards.
• Navigate tasks through multi‑functional teams during product development.

• Bachelor's or Master's degree in Systems Engineering, Biomedical Engineering, Electrical Engineering, or Mechanical Engineering.
• 5+ years of demonstrated ability in systems engineering (Med Tech industry preferred).
• Consistent track record of leading complex medical device development from concept to market.
• Strong knowledge of regulatory requirements and quality standards in the medical device industry (FDA, ISO 13485, ISO 60601).
• Excellent problem‑solving skills and ability to work effectively in a fast‑paced, collaborative environment.
• Strong communication and interpersonal skills, with ability to convey technical information to non‑technical stakeholders.
• Experience with requirement management tools (PTC, JAMA, or DOORS).
• Self‑motivated with ability to achieve results with minimal direction.
• Availability for up to 25% domestic and international travel.

• Prior clinical experience in critical care monitoring (hemodynamic monitoring, vital signs monitoring), interventional, vascular, or cardiac surgery.
• Good understanding of design controls (IEC 62366, ISO 14971, 21 CFR 820).
• Experience with Device Connectivity and Cloud‑based application solutions.

Location:

Irvine, CA

Salary: $ – $ USD annually

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.

At BD, we prioritize on‑site collaboration, fostering creativity, innovation, and effective problem‑solving. We encourage employees to bring their authentic selves to work and support learning, growth, and a culture of accountability. Join us to help reinvent the future of health and make the world a better place.