Jobs at Philips

Serve as the trusted technical lead for major healthcare accounts: act as single point of contact, ensure systems uptime, provide performance updates, monitor case trends, engage support to resolve escalations, and manage large software installations. Requires medical imaging, DICOM and HL7 expertise.

Lead the Advanced Development software workstream for ICE Imaging: define technical strategy, develop and validate ultrasound imaging, computer vision and AI algorithms, mentor engineers, manage cross-functional alignment, and transition research prototypes into regulated commercial medical products.

Design, build, and deploy enterprise AI solutions using LLMs, RAG, and AI agents. Develop AI-powered business apps with Microsoft Power Platform, create scalable data/AI solutions on Databricks using SQL and Python, integrate systems via REST APIs, and collaborate with stakeholders to prototype and operationalize intelligent automation.

The role involves defining and managing product roadmaps for a clinical software platform, collaborating with teams for product launch, and lifecycle management in the medical device sector.

Lead clinical input into robotic-assisted, image-guided therapy product development. Design and support clinical, preclinical, usability and evidence-generation studies, engage key opinion leaders, translate clinical workflows into design requirements, support physician education and conferences, and collaborate with cross-functional teams to validate innovations. Onsite in Cambridge, MA; travel up to 20%.

Lead global regulatory strategy and a Regulatory Affairs team for ambulatory monitoring and diagnostics. Oversee product registrations, 510(k) submissions, CE marking, clinical evaluations, audits, stakeholder engagement, and cross-functional integration to enable timely commercialization and sustained compliance.

The role involves leading software architecture for Clinical Imaging Software, ensuring compliance with regulations, and fostering technical excellence within the team.

Lead software design quality and regulatory compliance for medical device software across the lifecycle. Author and execute test protocols, perform root cause analysis, track anomalies, manage risk and traceability, drive regulatory submissions and approvals, and continuously improve software quality systems and processes to ensure safety and market access.

Define and drive systems engineering activities for distributed patient monitoring solutions. Collaborate with development, test, clinical engineering, and risk teams to model complex systems, derive system-level requirements, perform Software FMEA, and support integration of on-prem and cloud medical device and IT infrastructure.

Lead design quality and post-market complaint investigations for image-guided therapy products. Ensure design inputs/outputs, V&V, design transfer, risk management (ISO 14971), and design history files meet regulatory and quality standards. Perform post-market data analysis, initiate CAPA/field actions, and support continuous improvement across product lifecycle.

The Senior Clinical Scientist will lead clinical performance assessment, develop solutions strategies, collaborate on product roadmaps, and manage product development for ultrasound technologies.

The Senior Regulatory Affairs Specialist leads regulatory submissions for medical devices, provides guidance during product development, and ensures compliance with regulations.

Design and operate compliant, audit-ready data-quality and active-learning pipelines for medical imaging and metadata on cloud infrastructure. Build dataset versioning, de-identification, validation gates, lineage, and active-learning loops to prioritize labeling and measure label quality. Collaborate with AI engineers, clinicians, data stewards, and external annotation teams to deliver datasets fit for regulated medical-device software development.

Lead and manage a team of Design Quality Engineers to apply design controls, regulatory standards, and advanced statistical tools across product development. Support engineering teams on verification/validation, perform post-market risk assessments, facilitate FMEAs, and present risk findings to leadership to ensure product reliability and compliance with medical device regulations.

Verify and validate patient monitoring software through functional and automated testing. Report and document defects in a regulation-compliant manner, improve HW/SW test frameworks, develop automation and new protocols, and collaborate with clinical partners and cross-functional teams to refine healthcare solutions.

Manage commercial operations for complex hospital monitoring solutions, driving process documentation, handoffs (quoting → booking → delivery), phased license activations, pricing/invoicing accuracy, installation base records, escalation handling, and operational readiness. Lead process improvement and adoption of AI-enabled tools to scale Enterprise Monitoring and Connected Care subscription offerings across cross-functional teams.

The Software Design Quality Engineer assesses software designs, ensures compliance with regulatory standards, conducts root cause analyses, and manages software quality documentation throughout the lifecycle.

Lead design, implementation, integration, and support of complex infrastructure solutions across cloud and on-prem environments. Troubleshoot advanced issues, perform root-cause analysis, optimize performance, maintain configuration/version control, document procedures, and advise stakeholders. Drive interoperability, deployment strategies, and continuous improvement in a health‑tech context.

The Senior Clinical Development Scientist develops clinical/economic evidence for Philips Ultrasound products, collaborates with stakeholders, and leads clinical initiatives, ensuring compliance and innovation in clinical evidence.

The Integration Consultant leads technical implementation and support for the IECG system, managing interfaces with RIS/HIS, and troubleshooting complex issues.