Philips

4 weeks ago

Product Quality Engineer

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 14 hours agoStatus: Live

Job Summary

Drive factory quality engineering and assurance by monitoring and improving operations performance, supporting Supplier Quality Engineering/Assurance, and partnering with Purchasing. Assess the impact of design changes on PFMEA controls, analyze non-conformances and defects, and coordinate NC/QN and CAPA actions. Lead process validation and NPI/product transfer quality activities, using advanced statistical analysis to report metrics, improve quality standards, and ensure regulatory compliance.

Location: Israel

Workplace: Onsite

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Monitor and report operations performance, support improvement programs in the factory, and provide analytical testing support for SQE/SQA and Purchasing.
•Assess the impact of design changes on PFMEA and associated controls, and support manufacturing process development and design transfer activities.
•Lead defect and non-conformance analysis, drive NC/QN management, and facilitate effective CAPA implementation.
•Handle non-conformance events and investigations, and guide material review board activities for disposition management.
•Facilitate quality engineering/assurance tasks including process validation, NPI, and product transfers; analyze quality metrics and provide insights for continuous enhancement and regulatory compliance.

Key Requirements

•Bachelor’s / Master’s Degree in Mechanical Engineering, Electronics Engineering, Science, or equivalent.
•Minimum 2 years of experience (with a Bachelor’s) in Quality Engineering, Safety Engineering, or Process Engineering; or no prior experience required with a Master’s degree.
•Previous experience from medical device companies.
•Working knowledge of Quality Engineering and Continuous Improvement techniques, and ability to follow processes and operational policies.
•Ability to utilize statistical analysis methods to interpret quality data trends and support improvement initiatives.

Experience:2+ yearsMedical device

Education:Bachelor's in Mechanical Engineering, Electronics Engineering, Science

Skills:Stakeholder managementTraining deliveryAnalytical problem-solving

Tech Stack:Supplier Quality Engineering (SQE)Supplier Quality Assurance (SQA)PFMEACAPANon-Conformances (NC)Quality Notifications (QN)New Product Introduction (NPI)Process validationMaterial review boardStatistical analysis

Company Brief

Philips

Global health technology company focusing on diagnostic imaging, patient monitoring, and consumer health products. Philips develops medical devices, healthcare informatics, and solutions to improve patient care and personal well-being.

Industry: HealthTech

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Amsterdam, Netherlands

Founded: 1891

Glassdoor: 3.8

Website LinkedIn

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Philips

4 weeks ago

Product Quality Engineer

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 14 hours agoStatus: Live

Job Summary

Location: Israel

Workplace: Onsite

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Monitor and report operations performance, support improvement programs in the factory, and provide analytical testing support for SQE/SQA and Purchasing.
•Assess the impact of design changes on PFMEA and associated controls, and support manufacturing process development and design transfer activities.
•Lead defect and non-conformance analysis, drive NC/QN management, and facilitate effective CAPA implementation.
•Handle non-conformance events and investigations, and guide material review board activities for disposition management.
•Facilitate quality engineering/assurance tasks including process validation, NPI, and product transfers; analyze quality metrics and provide insights for continuous enhancement and regulatory compliance.

Key Requirements

•Bachelor’s / Master’s Degree in Mechanical Engineering, Electronics Engineering, Science, or equivalent.
•Minimum 2 years of experience (with a Bachelor’s) in Quality Engineering, Safety Engineering, or Process Engineering; or no prior experience required with a Master’s degree.
•Previous experience from medical device companies.
•Working knowledge of Quality Engineering and Continuous Improvement techniques, and ability to follow processes and operational policies.
•Ability to utilize statistical analysis methods to interpret quality data trends and support improvement initiatives.

Experience:2+ yearsMedical device

Education:Bachelor's in Mechanical Engineering, Electronics Engineering, Science

Skills:Stakeholder managementTraining deliveryAnalytical problem-solving

Company Brief

Philips

Industry: HealthTech

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Amsterdam, Netherlands

Founded: 1891

Glassdoor: 3.8

Website LinkedIn