Sr. Staff Systems Engineer

Becton Dickinson; Tempe (AZ); On-site; USD 130,000 - 190,000; Full time

Job summary

Becton, Dickinson and Company seeks a Sr. Staff Systems Engineer to lead development of complex electro‑mechanical medical technologies from concept to post‑market support.

You will shape architecture, define system requirements, and drive integration and verification while ensuring design control compliance. You will collaborate with cross‑functional teams, mentor engineers, and guide technical execution, addressing user needs, regulatory requirements, and performance expectations across the

Qualifications

• Validated experience in R&D for complex electro‑mechanical systems, medical devices, diagnostics, lab automation, or similar.
• Experience writing system level requirements and decomposing into hardware, software, usability and mechanical requirements.
• Experience with verification and validation protocols.
• Strong understanding of IEC 6060-1 and relevant medical device standards.

Responsibilities

• Lead systems level design and development activities for new and existing products.
• Define, maintain, and evolve system and product architectures, ensuring alignment with user needs, regulatory requirements, and business goals.
• Translate user and stakeholder needs into clear, actionable system requirements and interface definitions.
• Ensure complete traceability from requirements through design, implementation, verification, and validation.
• Lead and review product development plans, design reviews, technical documents, and formal reports.
• Review and approve verification and validation protocols and reports per BD design control procedures.
• Develop and implement design control‑related procedures/policies to ensure compliance with FDA/QSR, ISO 13485, and internal standards.

Skills

Systems engineering leadership

Mentoring engineers

Cross-functional collaboration

Requirements decomposition

Education

Bachelor’s degree in Engineering or Scientific field

Master’s degree or equivalent with 7+ years

Ph.D. or equivalent with 4+ years

Tools

Requirement management tools

Job description

We are the people who give possibilities purpose 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 MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

About the Role

We’re looking for a Sr. Staff Systems Engineer with a strong systems mindset to lead the development and evolution of complex medical technologies. In this role, you will shape system architecture, define system‑level requirements, drive integration and verification, and ensure full design control compliance throughout the product lifecycle; from concept through commercialization and post‑market support. You will collaborate with and lead cross‑functional teams while mentoring engineers as you guide the technical execution of highly complex electro‑mechanical medical devices. Your work ensures that our solutions meet user needs, regulatory requirements, and performance expectations. Whether you're passionate about systems thinking, product architecture, or hands‑on experimentation, this role offers the opportunity to make a meaningful impact on innovative healthcare solutions.

Key Responsibilities

• Lead systems level design and development activities for new and existing products.
• Define, maintain, and evolve system and product architectures, ensuring alignment with user needs, regulatory requirements, and business goals.
• Translate user and stakeholder needs into clear, actionable system requirements and interface definitions.
• Ensure complete traceability from requirements through design, implementation, verification, and validation.
• Lead and review product development plans, design reviews, technical documents, and formal reports.
• Review and approve verification and validation protocols and reports per BD design control procedures.
• Develop and implement design control‑related procedures/policies to ensure compliance with FDA/QSR, ISO 13485, and internal standards.
• Lead system integration activities, including defect tracking, configuration management, and risk assessment.
• Plan, execute, and analyze system‑level testing, then effectively communicate insights.
• Critique and guide engineering test method development and simulated‑use methods; oversee validation of these methods.
• Support test equipment development and IQ/OQ/PQ validation where applicable.
• Lead cross‑functional technical reviews and risk management activities (dFMEA, hazard analysis).
• Work with marketing, sales, and clinicians to define high‑level system requirements and workflows.
• Provide system‑level guidance on DFM/DFSS, manufacturability, and subsystem integration.
• Ensure clear documentation of subsystem level design requirements.
• Ensure accurate communication of relevant requirements for all cross functional stakeholders.
• Apply creative problem‑solving and critical thinking to resolve complex technical challenges.
• Lead idea generation and IP development activities; support patent submissions for system innovations.
• Develop project plans to assess complex technologies and drive execution.
• Create, lead, and control project technical budget and perform cost analyses.
• Identify and implement system‑level cost improvements.
• Support Manufacturing, Quality, Regulatory, and Sustaining Engineering to ensure compliance.
• Lead or support root cause investigations, non‑conformances, and complaint analyses.
• Mentor and coach engineers and technicians.
• May supervise engineers/technicians and participate in performance feedback and hiring processes.

Required Education

• Bachelor’s degree in Engineering (Mechanical, Electrical, Biomedical, Software) or Scientific field & 8 + years of experience.
• – OR – Master’s Degree or equivalent in Engineering or Scientific field & 7+ years of experience with test method development and writing test plans is required.
• – OR – Ph.D. or equivalent in Engineering or Scientific field & 4+ years of experience with test method development and writing test plans is required.

Required Experience & Qualifications

• Validated experience in R&D for complex electro‑mechanical systems, medical devices, diagnostics, lab automation, or similar.
• Previous experience working with requirement management tools such as Modern Requirements, PTC, Polarion, JAMA or DOORS.
• Experience writing system level requirements and working with different functional groups to decompose into hardware, software, usability and mechanical requirements.
• Experience with writing and execution system verification and validation protocols.
• Strong understanding of IEC 6060-1 and relevant medical device standards.
• Solid base in systems engineering principles, including requirements management, architecture development, integration, and verification.

Preferred Qualifications

• Comfortable navigating ambiguity and driving clarity in fast‑paced, agile environments.
• Effective communicator and collaborator with the ability to influence across functions and lead without formal authority.
• Demonstrated ability to lead technical complexity and deliver results in cross‑functional project teams.
• Self‑motivated, curious, and eager to learn new technologies and approaches.

Travel Requirements

This position requires 15‑25% travel to support system‑level development activities. Travel may include visits to BD design centers, manufacturing sites, supplier facilities, and preclinical or clinical environments. A large portion, especially during onboarding, will involve regular collaboration with our engineering teams in Ireland, including onsite work to support system integration builds, design reviews, verification and validation activities, and cross‑functional alignment.

Physical Demands

Regular standing, walking, sitting, verbal communication; occasional reaching, kneeling, crouching.

Work Environment

Will work in office, lab, preclinical, or clinical case environments.

BD is an equal opportunity employer. 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.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face‑to‑face collaboration supports your learning, your progress, and your success. To learn more about BD visit https://bd.com/careers.

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.

Primary Work Location USA AZ - Tempe Headquarters Additional Locations Work Shift

We are the #MakersofPossible Working together, we make products that patients, families and their healthcare professionals rely on. We do this because we are committed to advancing the world of health™. But it takes the imagination and passion of all of us at BD, from manufacturing to marketing, to look at the impossible and find solutions that turn dreams into possibilities with real‑life health benefits for people today, tomorrow and beyond. We make this happen, together. We are the makers of possible.

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.