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Philips

Makes medical devices and personal health products

Product Quality Engineer

Quality EngineeringConfirmed live in the last 24 hours
Full-timeHaifa, Israel₪20k - ₪25k

About the Job

Requirements

  • A bachelor's degree in Industrial Engineering, Quality Engineering, or equivalent is required.
  • At least 2 years of experience in Quality Engineering, Process Engineering, or a related field is required.
  • Experience working in a manufacturing environment is required.
  • Experience with root-cause analysis, quality improvement, and manufacturing processes is required.

Responsibilities

  • Own and drive quality performance of manufacturing processes to ensure they consistently meet defined quality, regulatory, and product requirements.
  • Monitor process quality performance using KPIs such as First Time Right (FTR), DPU/DPMO, yield, defects, rework, scrap, and process capability.
  • Identify process quality risks and lead initiatives to reduce process variation, defects, and quality escapes.
  • Perform structured root-cause analysis of manufacturing defects and process failures using 5-Why, Fishbone, 8D, DMAIC, and other problem-solving methodologies.
  • Lead and facilitate investigations of Non-Conformances (NCs), Quality Notifications (QNs), and manufacturing-related quality issues.
  • Define and implement effective containment, corrective, and preventive actions to eliminate process-related defects and prevent recurrence.
  • Provide quality input to PFMEA, Control Plans, process flows, work instructions, and manufacturing documentation.
  • Support and lead process validation and re-validation activities, including protocol development, execution, data analysis, and validation reports.
  • Support NPI, design transfer, and production ramp-up, ensuring appropriate quality controls are established before production release.
  • Work closely with Manufacturing, Process Engineering, R&D, PQE, SQE, Supplier Quality, and Operations to resolve complex process-quality issues.
  • Establish and monitor process quality control plans and ensure effective implementation on the production floor.
  • Analyze quality trends regularly and identify emerging process risks before they result in significant quality events or customer impact.
  • Participate in internal and external audits and provide technical support related to manufacturing process controls and quality.

Desired Qualifications

  • Experience in medical devices or another regulated industry.
  • Experience with PFMEA, Control Plans, and process validation.
  • Experience with NC, QN, CAPA, and change management processes.

About the Company

Philips

Makes medical devices and personal health products

Philips makes medical equipment and software for hospitals and care providers, along with personal health products for consumers. Its hospital portfolio spans MRI and CT scanners, ultrasound, image-guided treatment systems and patient monitors, while Sonicare and Avent cover oral health and baby care. Clinical software connects medical images and patient data across care teams, and the company earns revenue from equipment, software, maintenance and consumer product sales. It works with health systems through long-term technology and service partnerships, including solutions for care at home. Founded in 1891, Philips is headquartered in Amsterdam, the Netherlands.

Company size
10,001+
Company stage
Acquired
Total funding
$164.7M
Headquarters
Andover, MN
Founded
1891

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