You are responsible for ensuring appropriate quality plans are made and executed throughout the product lifecycle to improve people’s health
Job Summary
You are responsible for ensuring appropriate quality plans are made and executed throughout the product lifecycle to improve people’s health.
You will provide leadership and oversight to ensure compliance with Quality Management Systems and apply best practices in design quality and reliability.
Philips embraces a hybrid work model promoting flexibility, collaboration, and a culture of inclusion and diversity to foster patient safety and quality.
Matching Summary
You are responsible for ensuring appropriate quality plans are made and executed throughout the product lifecycle to improve people’s health.
Skills & Requirements
Must-have
Quality Plan design and execution
Risk Management activities
Post-market product quality analysis
Quality Management System Compliance
Design for Quality & Reliability practices
Software quality management in Medtech
Nice-to-have
Data analysis and performance dashboards
Root cause analysis and problem solving
Understanding of software development methodologies
Passion for patient safety and quality
Hybrid work flexibility
Collaboration and inclusion culture
Key Requirements
Engineering Graduate in computer science or related field
12 years technology industry experience
Minimum 8 years in software quality management within Medtech
Expertise in ISO 13485, ISO 14971, IEC 82304, IEC 62366, EUMDR, 21CFR820
Experience with design controls, CAPA, complaint handling
Proficient in software tool validation and correction/removals