In this role, you have the opportunity to

System Verification Manager role is to lead system-level verification strategy, execution, and team development for our ultrasound platforms. This role ensures that all product design outputs are fully verified against design inputs, regulatory, and quality requirements, supporting fast and compliant product delivery.

The role will drive end-to-end System Verification capabilities, including verification planning, execution, automation, compliance, and team excellence across Local-for-Local (L4L) and global projects.

You are responsible for

• Own overall System Verification function, deliverables, and quality of outputs,
• Build and lead a high-performing System Verification team (System integration, automation, verification, clinical validation), Define and secure verification resources allocation across projects
• Define competency framework, hiring, coaching, and career development for system verification team
• Drive team engineering excellence, automation capability, and productivity improvement
• Define verification strategy, scope, and approach aligned with PDLM, IEC 62304, and ISO 14971
• Establish and govern entry, suspension, and exit criteria for System Verification
• Responsible for the planning, coordination and tracking of the System Verification activities, including but not limited to the verification plan, specifications, test cases, testing result and report, defects record and tracking.
• Ensure high-quality System Verification Reports supporting regulatory submissions.
• Ensure System verification activities are executed in compliance with Philips QMS and global procedures
• Drive continuous improvement in verification methodologies, automation, and tools
• Ensure audit readiness for NMPA, IEC, and internal quality audits
• Partner with RA, Quality, and System Engineering to ensure full compliance
• Interface with System Engineering, Software, Hardware, Clinical, RA, Manufacturing, and global teams
• Collaborate with Project Management to align verification plans with schedule, scope, and cost
• Support NMPA submission, deficiency response, and regulatory engagements
• Drive strong collaboration between China R&D and global verification teams

You are a part of

A progressive and energetic team that contributes directly to the growth of the business. You have a direct reporting line to the GRC System and Software Manager

To succeed in this role, you should have the following skills and experience

• Bachelor’s or above Degree in Engineering, the better major in biomedical engineering, electronic engineering or computer science.
• At least 10 years’ experience in design verification, validation, system engineering related position.
• At least 3+ years in technical leadership or team management role
• Medical products’ experience, V-model product development lifecycle process.
• Strong interpersonal and communication skills with the ability to communicate with different functions, e.g. System, Physics, SW, etc.
• Good knowledge of the English language (both written and verbal)