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ICC CAPA Owner/Scrum Master - Job Opportunity at Philips

Best, Netherlands
Full-time
Senior
Posted: May 22, 2025
Hybrid
EUR 52,000 per year

Benefits

25 days annual leave with option to purchase 20 additional days
Performance-based variable bonus
Comprehensive personal development budget
International work environment
Competitive pension scheme
Collective health insurance
Employee stock purchase program with discounts
Product purchase discounts

Key Responsibilities

Lead CAPA process implementation and quality assurance initiatives
Drive cross-functional investigations and root cause analyses
Implement data analytics for quality trend identification
Manage stakeholder communications and alignment
Ensure regulatory compliance and documentation
Support team prioritization and backlog management
Facilitate scrum processes and team efficiency

Requirements

Education

Bachelor's degree in Physics, Electrical Engineering, Biomedical Engineering, Computer Science or related field

Experience

5+ years in Research and Development within medical device industry

Required Skills

Project management Root cause analysis Quality management principles Stakeholder management Medical device regulatory compliance Data analytics Scrum methodology Cross-functional team leadership Documentation practices

Certifications

ASQ Certified Quality Engineer (preferred) Six Sigma Green or Black Belt (preferred)
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Sauge AI Market Intelligence

Industry Trends

Increasing focus on quality management integration with agile methodologies in medical device development Growing importance of data-driven quality assurance in healthcare technology Rising regulatory scrutiny in medical device manufacturing Shift towards hybrid quality management roles combining technical and process expertise

Salary Evaluation

EUR 65,000 - 85,000 based on role complexity and market conditions in Netherlands medical device sector

Role Significance

Typically leads cross-functional teams of 8-12 members across R&D, quality, and regulatory functions
Senior technical leadership position combining quality management and agile methodologies

Key Projects

Medical device compliance initiatives Quality system improvements Product development process optimization Regulatory audit preparation

Success Factors

Deep understanding of medical device regulations and quality systems Strong technical background in imaging systems Excellent stakeholder management skills Ability to balance quality requirements with development efficiency

Market Demand

High demand due to increasing regulatory requirements and quality focus in medical device industry

Important Skills

Critical Skills

Medical device quality management expertise Root cause analysis proficiency Regulatory compliance knowledge Agile methodology implementation

Beneficial Skills

X-ray physics understanding Medical imaging technology knowledge Six Sigma certification International team experience

Unique Aspects

Combination of quality management and agile methodologies
Focus on advanced medical imaging technology
Strong emphasis on regulatory compliance
Global impact on healthcare delivery

Career Growth

2-4 years in role before advancement, depending on project success and organizational growth

Potential Next Roles

Quality Management Director R&D Program Manager Technical Operations Leader Regulatory Affairs Manager

Company Overview

Philips

Global leader in health technology, focusing on diagnostic imaging and minimal invasive therapy solutions

Strong market position in medical imaging technology with significant R&D investment
Major technical hub in Best, Netherlands, with global impact on healthcare technology
Innovation-driven environment with strong focus on quality and regulatory compliance
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