Process Quality Engineer — Medical Devices & CAPA

Philips; Best; On-site; EUR 48,000 - 81,000; Full time

Job summary

Philips in Best, Netherlands seeks a Process Quality Engineer to drive high-quality performance and compliance across factories while pursuing continuous improvement. You will analyze defects, manage non-conformances and CAPA, support PFMEA assessments and design changes, and coordinate quality activities across manufacturing and supply chains.

You will also contribute to risk assessment, analytics reporting, and supplier quality collaboration, while supporting process validation and product

Qualifications

• Bachelor’s degree in Quality, Engineering or similar discipline is required and relevant experience is valued.
• 2+ years in FDA regulated medical device quality/manufacturing environments with CAPA, non-conformance and change management experience.
• Strong data analytics skills and ability to interpret quality metrics and trends.
• Experience with PFMEA and design transfer is preferred.

Responsibilities

• Analyzes defects for dispositions of non-conformances and drives NC and QN management, implementing CAPA actions.
• Assesses PFMEA impact related to design changes and supports manufacturing process development and design transfer.
• Supports operations performance monitoring, risk assessment, reporting, and supplier quality engineering activities.
• Coordinates quality engineering tasks and maintains manufacturing quality systems across the factory.
• Develops cross-functional improvements and applies basic quality engineering principles to drive process improvements.

Skills

Quality engineering

CAPA

PFMEA

Data analytics

Education

Bachelor’s Degree in Quality or Engineering

Tools

Quality Management Systems

Job description

Philips in Best, Netherlands seeks a Process Quality Engineer to drive high-quality performance and compliance across factories while pursuing continuous improvement. You will analyze defects, manage non-conformances and CAPA, support PFMEA assessments and design changes, and coordinate quality activities across manufacturing and supply chains.

You will also contribute to risk assessment, analytics reporting, and supplier quality collaboration, while supporting process validation and product