Jobs at Philips

Lead and govern enterprise-wide software and device firmware releases for ECG solutions, plan deployments aligned to Agile increments, track KPIs, manage risks/dependencies, improve release processes, ensure regulatory compliance (FDA/ISO/NIST/HIPAA), and coordinate cross-functional teams to deliver high-quality releases.

Coordinate day-to-day quality activities including managing daily boards, quality notifications, delivery holds, and tracking metrics. Lead investigations, CAPA, root cause analysis, and supplier quality interactions. Maintain QMS/eQMS, document control, training records, and support audits to ensure regulatory compliance and timely resolution of quality issues.

Lead oversight of hardware and system quality, safety risk management, and design verification/validation across the product lifecycle for medical devices. Provide independent technical assessments, ensure design transfer and compliance to regulatory standards, and act as single quality contact for project milestones.

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.

Provide transactional HR and payroll administration including master data changes, onboarding, time & attendance, leave and termination processing. Ensure data integrity and compliance, support payroll reporting, use AI and digital tools for process improvements, coordinate vendors, and participate in LEAN initiatives to optimize HR operations.

Manage and coach a small production team, optimize manufacturing KPIs, implement Lean and NPI processes, ensure safety and quality compliance, develop financial forecasts and operating plans, and drive continuous improvement.

Design, develop, and deliver advanced clinical Neuro MR software features from concept through validation and release. Lead architecture, prototyping, IQ optimization, and cross-functional collaboration with clinical teams while ensuring regulatory-compliant, high-quality implementations and mentoring peers.

This role involves executing sales plans for ultrasound products, ensuring strategic alignment, maintaining CRM records, supporting stakeholders, and analyzing market data to drive sales and operational efficiency.

Support and execute quality control activities for medical-device manufacturing, troubleshoot process abnormalities, drive validation and documentation, uphold GLP/GMP, perform statistical analysis using SPC and Minitab, manage CAPA and problem‑solving methodologies, and ensure safety and regulatory compliance while working with limited supervision.

Lead architecture and design for product/platform DevOps within release trains, ensuring nonfunctional requirements, regulatory compliance (e.g., FDA), and alignment with stakeholders. Mentor scrum teams, drive reuse of platforms and technologies, engage in technical negotiations, and contribute to code development and integration planning over a 6–12 month horizon.

Manage and grow strategic retail accounts through end-to-end account management: business planning, commercial negotiations, promotional execution, sales tracking, and customer development. Develop account plans, lead joint business planning and reviews, manage budgets and trade spend, ensure excellent in-store execution, provide data-driven recommendations, and collaborate cross-functionally to achieve sales, market share, and profitability targets.

Lead a cross-functional Scrum team to design, build and run cloud-native full-stack applications on a Kubernetes platform. Provide technical stewardship, mentor engineers, implement TDD and automated tests, design backend APIs and front-end React apps, optimize data models (SQL/NoSQL), integrate CI/CD, observability, and collaborate with platform/security teams to ensure reliable production deployments.

Lead quality engineering for sleep and respiratory care products, ensuring design and post-market compliance with medical device regulations. Support quality plans, risk management, reliability and PMS, perform technical assessments, root cause analysis, audits, and initiate field actions as needed.

Support reliability activities across product development: write test protocols/reports, execute ALT/HALT/HASS and durability testing, perform life analysis, contribute to FMEAs/FTAs, collaborate cross-functionally, and assist in root cause analysis and corrective action verification.

Develop, test, review, and deploy Java Spring Boot microservices and Angular front-ends. Design APIs, resolve defects, support DevOps/CI-CD, create documentation, and collaborate in Agile teams to meet performance and quality metrics.

Lead design quality assurance for medical device development and sustaining projects. Manage design controls, design history files, risk management, post-market surveillance integration, CAPA, audits, regulatory submission support, data analysis, and transfer of quality deliverables to manufacturing and supplier quality teams.

Develop, optimize and validate CT reconstruction algorithms (correction, analytic/iterative reconstruction, deep learning). Work on preprocessing, denoising, artifact correction, low-dose methods, dose optimization, detector/X-ray physics analysis, algorithm prototyping in Matlab, simulation, engineering handoff, clinical validation and documentation.

Lead electrical design, verification and validation for interventional X-ray systems. Define electrical requirements, perform electronics design and EMC/safety testing (IEC60601), create test strategies and plans, coordinate with cross-functional teams and suppliers, and support lab compliance, prototype acceptance and new product introduction/lifecycle activities.

Develop and maintain a controlled AI R&D Harness for medical-device QMS: build production-grade AI services (RAG, prompts, agents), integrate read-only with enterprise systems, implement audit/logging/access controls, support validation (OQ/PQ) with test harnesses and datasets, partner with SMEs and quality/regulatory teams, and document/configure controlled deployments.

Develop, optimize, and validate core CT reconstruction algorithms (correction, basic and iterative reconstruction, deep learning). Work on CT preprocessing, denoising, artifact correction, low-dose optimization, detector response and X-ray attenuation modeling. Prototype algorithms (mainly MATLAB), perform simulation and testing, support engineering productization, document results, and lead cross-functional clinical validation and regulatory-aligned verification.