Job Title

Senior Hardware System Architect

Job Description

CT HW System Architect Engineer

An experienced CT Hardware Subsystem Architect Engineer to define, develop, and govern the architecture of critical hardware subsystems for next-generation CT HW platforms. The architect will be responsible for establishing subsystem architecture, defining technical roadmaps, driving key technology decisions, managing subsystem interfaces, and ensuring that subsystem performance, reliability, safety, manufacturability, serviceability, and cost targets are achieved.

Your role:

• Own the end-to-end architecture of the assigned CT HW subsystem.

• Lead architecture reviews and critical design reviews, Serve as primary technical authority for the subsystem.

• Define subsystem architecture strategy aligned with platform roadmap.

• Develop subsystem technical requirements and architecture specifications.

• Ensure architecture supports future scalability and platform reuse.

• Drive architectural trade-offs for balancing performance, reliability, complexity, cost, and schedule.

• Ensure architecture supports future platform scalability and technology evolution.

• Analyze system requirements, clinical needs, product requirements, and regulatory requirements, flow down to subsystem and critical components.

• Allocate subsystem performance budgets and margins, establish and maintain complete end-to-end traceability throughout the development lifecycle.

• Establish and maintain complete end-to-end traceability throughout the development of lifecycle.

• Define subsystem interfaces, lead interface reviews, and integration planning.

• Ensure subsystem architecture supports lifetime reliability and field performance requirements.

You're the right fit if:

• Master or Bachelor's degree in Engineering (Electrical, Electronics, Systems Engineering, or related discipline).

• 10+ years of system engineering experience.

• 6+ years of architecture ownership or technical leadership and demonstrated experience for complex medical devices (CT, MR, X-ray, Radiation Therapy), imaging systems, industrial automation, aerospace, automotive, or other highly regulated systems.

• Solid working knowledge of ISO13485, EU MDR, FDA 21 CFR, ISO14971.

• Ability to translate regulatory and safety requirements into subsystem architecture, requirements, risk controls, and verification plans.

• Strong and practical knowledge on DFMEA, problem solving, prefer Design For Six Sigma (GB/BB) certified candidates.

How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 4 days per week.
Onsite roles require full-time presence in the company’s facilities.
Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
Indicate if this role is an office/field/onsite role.

About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here.