Philips

3 weeks ago

Verification 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

Lead product verification activities to ensure built-in quality throughout the development lifecycle. Drive functional, performance, load, and reliability testing (automated or manual) across feature, sub-system, and system levels, define test strategies, and establish design verification entry/exit criteria. Review requirement and design specifications for testability and sufficiency, plan and track design verification work, document plans/records/reports, manage defects, and develop automation scripts, while supporting design changes for quality impact.

Location: China

Workplace: Onsite

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Lead and support product verification activities to ensure compliance with QMS and deliver high-quality products to customers.
•Perform product testing (automated or manual) across the full development cycle within systems/agile/scrum teams to ensure built-in quality.
•Provide test expertise to define and drive product test strategies and initiatives at feature, sub-system, and system level.
•Review system and product design/requirement specifications and risk/safety/regulatory documentation; estimate testability and sufficiency.
•Plan, coordinate, and track design verification activities; establish entry/exit criteria; document plans/specs/records/reports; report defects and track issue resolution; support design changes for quality impact.

Key Requirements

•Bachelor’s degree or above in Engineering (biomedical engineering, electronic engineering, computer science, or software engineering).
•At least 10 years of experience in product verification.
•At least 5 years working experience with medical products.
•Knowledge of the V-model development cycle.
•Knowledge of IEC 60601 and ISO 13485 and 21 CFR 820 is preferred.

Experience:10+ yearsMedical devicesMedical productProduct verification

Education:Bachelor's in Engineering (biomedical engineering, electronic engineering, computer science, or software engineering)

Skills:Interpersonal skillsCommunication skills

Certifications:ISTQB

Languages:English

Tech Stack:QMSV-modelIEC60601ISO1348521CFR820HardwareEmbedded softwareAuto-test softwareAgileScrumAutomation scripts

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

3 weeks ago

Verification 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: China

Workplace: Onsite

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Lead and support product verification activities to ensure compliance with QMS and deliver high-quality products to customers.
•Perform product testing (automated or manual) across the full development cycle within systems/agile/scrum teams to ensure built-in quality.
•Provide test expertise to define and drive product test strategies and initiatives at feature, sub-system, and system level.
•Review system and product design/requirement specifications and risk/safety/regulatory documentation; estimate testability and sufficiency.
•Plan, coordinate, and track design verification activities; establish entry/exit criteria; document plans/specs/records/reports; report defects and track issue resolution; support design changes for quality impact.

Key Requirements

•Bachelor’s degree or above in Engineering (biomedical engineering, electronic engineering, computer science, or software engineering).
•At least 10 years of experience in product verification.
•At least 5 years working experience with medical products.
•Knowledge of the V-model development cycle.
•Knowledge of IEC 60601 and ISO 13485 and 21 CFR 820 is preferred.

Experience:10+ yearsMedical devicesMedical productProduct verification

Education:Bachelor's in Engineering (biomedical engineering, electronic engineering, computer science, or software engineering)

Skills:Interpersonal skillsCommunication skills

Certifications:ISTQB

Languages:English

Tech Stack:QMSV-modelIEC60601ISO1348521CFR820HardwareEmbedded softwareAuto-test softwareAgileScrumAutomation scripts

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