Philips

1 week ago

Site Quality Leader

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 12 hours agoStatus: Live

Job Summary

Lead site quality management as the Site Quality Management Representative, owning product quality and compliance to applicable standards. Set operational objectives, delegate execution, and drive a culture of quality. Monitor KPIs, guide audits and assessments, support regulatory compliance gap closure, and oversee supplier quality metrics. Manage and develop talent across the quality assurance team while implementing QMS and quality strategies aligned with organizational goals.

Location: China

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Seniority: Manager level

Key Responsibilities

•Serve as Site Quality Management Representative with overall responsibility for product quality, compliance, and a culture of quality at the site.
•Establish operational objectives and work plans; delegate assignments and collaborate across the organization to execute quality initiatives.
•Review and monitor operational KPIs, and participate in development/modification/execution of policies affecting operations.
•Lead product review and approvals, manage inspections, and coordinate with relevant groups to ensure compliance with standards, regulations, and manufacturing process specifications.
•Own audit and assessment processes, support internal/external audits, help close regulatory compliance gaps, and monitor supplier quality metrics while supporting supplier quality communications.

Key Requirements

•Bachelor’s or Master’s degree in Quality Management, Supply Chain Management, Engineering discipline, Science, or equivalent.
•Minimum 5 years of experience (Bachelor’s) or 3 years of experience (Master’s) in medical device, quality assurance/control, quality audit, compliance coordination, or warehouse operations.
•Working knowledge of international standards such as ISO 13485, ISO 9001, and ISO 14971.
•Experience with quality assurance (QA) and quality management systems (QMS), including continuous improvement approaches like CAPA.
•People management experience, with familiarity in supplier quality management, risk management, and regulatory compliance.

Experience:3+ yearsMedical deviceQuality assuranceQuality controlQuality auditCompliance coordinationWarehouse operations

Education:

Skills:Continuous improvementRisk managementStrategic planningBusiness acumenPeople management

Tech Stack:ISO13485ISO9001ISO14971Quality Management Systems (QMS)CAPAKPI management

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

1 week ago

Site Quality Leader

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 12 hours agoStatus: Live

Job Summary

Location: China

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Seniority: Manager level

Key Responsibilities

•Serve as Site Quality Management Representative with overall responsibility for product quality, compliance, and a culture of quality at the site.
•Establish operational objectives and work plans; delegate assignments and collaborate across the organization to execute quality initiatives.
•Review and monitor operational KPIs, and participate in development/modification/execution of policies affecting operations.
•Lead product review and approvals, manage inspections, and coordinate with relevant groups to ensure compliance with standards, regulations, and manufacturing process specifications.
•Own audit and assessment processes, support internal/external audits, help close regulatory compliance gaps, and monitor supplier quality metrics while supporting supplier quality communications.

Key Requirements

•Bachelor’s or Master’s degree in Quality Management, Supply Chain Management, Engineering discipline, Science, or equivalent.
•Minimum 5 years of experience (Bachelor’s) or 3 years of experience (Master’s) in medical device, quality assurance/control, quality audit, compliance coordination, or warehouse operations.
•Working knowledge of international standards such as ISO 13485, ISO 9001, and ISO 14971.
•Experience with quality assurance (QA) and quality management systems (QMS), including continuous improvement approaches like CAPA.
•People management experience, with familiarity in supplier quality management, risk management, and regulatory compliance.

Experience:3+ yearsMedical deviceQuality assuranceQuality controlQuality auditCompliance coordinationWarehouse operations

Education:

Skills:Continuous improvementRisk managementStrategic planningBusiness acumenPeople management

Tech Stack:ISO13485ISO9001ISO14971Quality Management Systems (QMS)CAPAKPI management

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