R&D Engineer

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R&D Engineer - X-ray Detector Verification

Location Best, Noord-Brabant, Netherlands Job Type Full time Job Id 565724 Posted Date: 12/18/2025

JOB DESCRIPTION

Job Title

R&D Engineer - X-ray Detector Verification

Job Description

Join Philips as an X-ray Detector Verification Engineer in the Imaging Chain Cluster, where you'll ensure the quality and reliability of X-ray detectors used in advanced imaging systems. This role focuses on verifying detectors according to the V-model, meeting user and business requirements while complying with stringent regulatory standards.

Your role:

• Your work directly supports the delivery of safe, high-performing imaging solutions that enable healthcare professionals to provide superior patient care.
• You'll be part of the X-ray components team (~20 engineers) within the Imaging Chain Cluster (ICC) in the Image Guided Therapy Systems (IGT-S) organization at Philips in Best, NL. You'll collaborate with multidisciplinary teams in R&D, Lifecycle Management, and external suppliers, as well as Philips businesses (IGT-S, DXR, MoS).
• Exposure to cutting-edge medical imaging technology, opportunities to contribute to New Product Introduction (NPI) and Life Cycle Management (LCM) projects, and growth in regulatory compliance expertise.
• Other Responsibilities:
  • Verification of flat panel detectors in collaboration with internal businesses and suppliers.
  • Documentation of verification and validation evidence per regulatory standards.
  • Support factory and service organizations in resolving quality issues.
  • Apply analytical and problem-solving skills to tackle technical challenges and drive continuous improvement.

You're the right fit if:

• 3+ years in verification, validation, or R&D within a high-tech or medical device environment.
• Strong analytical mindset, problem-solving ability, attention to detail in testing and documentation; experience with X-ray imaging systems or flat panel detectors.
• Bachelor's degree in Electrical Engineering, Applied Physics, Medical Engineering, or related technical field.
• Familiarity with ISO 13485, ISO 14971, IEC 60601, FDA 820 standards.
• Excellent collaboration and communication skills in multidisciplinary, international teams.
• Proactive, quality-focused, and eager to contribute to innovation in healthcare technology.