Jobs at Philips

Provides Level 3 technical support for Philips healthcare products, diagnosing complex hardware, software, networking, and configuration issues. Leads global product support strategy, escalation resolution, service processes, reliability monitoring, training, communications, continuous improvement, and end-of-life planning. Partners with field teams, customers, R&D, and functional management to improve product performance, reduce ownership costs, and increase customer satisfaction.

Develop and test full-stack software for a real-time hospital patient monitoring platform. Responsibilities include designing scalable and reliable components, writing technical specifications, implementing software solutions, reviewing code, mentoring engineers, optimizing performance, and applying engineering best practices in an Agile environment. The role uses C#, .NET, React, GraphQL, databases, and cloud-native technologies while collaborating with cross-functional teams.

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%.

Supports market sizing and forecasting models, analyzes market trends and competitive dynamics, and translates data into actionable enterprise insights. Collaborates with global stakeholders across business units, regions, and functions while improving analytical tools, datasets, and methodologies. The role requires expertise in competitor analysis, data analytics, forecasting, market modeling, KPI reporting, and business case analysis.

Owns and governs corrections and removals processes for medical devices, ensuring regulatory compliance, risk-based controls, documentation, consistency, and continuous improvement. The role develops process frameworks, manages change requests, identifies operational gaps and risks, supports knowledge sharing, and evaluates AI and digital tools for efficiency and decision support. It requires substantial experience in corrections and removals, field actions, post-market surveillance, and global medical device regulations.

Owns the sustaining lifecycle strategy and prioritized backlog for regulated MCT and Holter hardware. The role coordinates product changes, supplier and obsolescence actions, manufacturing and service improvements, labeling updates, issue resolution, quality and regulatory activities, and supply continuity planning. The manager monitors product health, drives corrective actions, supports transition and end-of-life plans, and aligns Sales, Marketing, Service, Operations, Quality, Regulatory, and regional stakeholders.

Lead global commercialization and marketing execution for an advanced imaging portfolio. Develop value propositions, pricing, go-to-market plans, launch campaigns, and annual marketing strategies. Partner with regional marketing, sales, clinical, regulatory, medical affairs, and market access teams to drive adoption and business growth. Provide messaging, training, and commercial tools while using market, competitive, financial, and customer insights to optimize performance. Build KOL relationships and lead cross-functional initiatives in a global matrixed environment.

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.

Leads KOL strategy and engagement by identifying and cultivating clinical, technical, operational, and executive advocates. Develops customer activation plans, manages outreach and reference-site programs, coordinates advisory councils and speaking engagements, and creates customer success stories, case studies, testimonials, and marketing materials. Measures program performance and supports customer advocacy, peer-to-peer engagement, and strategic business objectives.

Leads quality operations for advanced imaging medical devices, managing CAPA, nonconformances, process validation, risk management, supplier quality, audits, and continuous improvement. Oversees manufacturing process development, design transfer, NPI, quality systems, and regulatory compliance. Manages quality personnel, including workforce planning, performance management, coaching, budgeting, and succession planning. Collaborates with R&D, manufacturing, regulatory teams, suppliers, and internal stakeholders to ensure product quality and operational excellence.

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 sales operations strategy and contract management, overseeing drafting, negotiation, execution, compliance, risk mitigation, process improvement, technology optimization, and talent development to align sales activities with business goals.

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

As Global Product Manager, you'll define product strategies for mobile applications, oversee product lifecycle, and lead go-to-market efforts. You'll collaborate with cross-functional teams to address customer needs and improve product performance.

Lead and oversee the QMS and design assurance for Image Guided Therapy products, drive regulatory compliance (FDA, MDR, ISO), manage quality teams, lead audits and inspections, direct CAPA and root-cause investigations, apply risk management and continuous improvement (Lean/Six Sigma), and partner cross-functionally to ensure product safety and performance.

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 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.

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 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.

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.