Philips

5 days ago

Sr. Supplier Quality Engineer

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 11 hours agoStatus: Live

Job Summary

Own supplier quality engineering for the Costa Rica facility, aligning site Quality, Manufacturing, R&D, Procurement, and supplier partners to ensure compliant, high-performing supplier processes. Lead and manage APQP/PPAP activities and supplier validation readiness using quality planning and controls (MSA, PFMEA, Control Plan, SPC, PV&V, IQ/OQ/PQ, FAI). Drive supplier audits, qualifications, non-conformance investigations, SCAR/CAPA execution, and systemic supplier improvement in a regulated medical-device environment.

Location: Costa Rica

Workplace: Hybrid

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Serve as the primary Supplier Quality Engineering point of contact for the Costa Rica facility, providing remote site support and aligning stakeholders across Quality, Manufacturing, R&D, Sustaining Engineering, and Procurement.
•Lead and own supplier quality documents and activities including MSA, PFMEA, Control Plan, SPC, PV&V, FAI, IQ/OQ/PQ, and APQP/PPAP to ensure process capability and compliance.
•Lead APQP/PPAP execution for supplier transfers, supplier changes, SICRs, and sustaining projects supporting the Costa Rica manufacturing facility.
•Facilitate Design for Excellence collaboration to improve design quality, manufacturability, supplier process robustness, and long-term product performance.
•Lead supplier audits and supplier qualification/approvals, and manage supplier non-conformance investigations and Supplier Corrective Action Requests (root cause, CAPA, verification, and closure).

Key Requirements

•7 years of experience in Quality, Manufacturing, or Supplier Quality Engineering, preferably in regulated industries such as medical devices.
•Strong expertise in supplier quality management, audits, root cause analysis, CAPA methodologies, process validation, and continuous improvement.
•Bachelor’s degree in Engineering, Supply Chain Management, Electrical/Electronic Engineering, or related field.
•Working knowledge of global medical device regulations and standards, with familiarity with statistical tools and quality methods.
•Strong cross-functional collaboration skills and a proactive, risk-based mindset.

Experience:7+ yearsMedical devicesRegulated industries

Education:Bachelor's in Engineering, Supply Chain Management, Electrical/Electronic Engineering, or a related field

Skills:Cross-functional collaborationRisk-based mindsetContinuous improvementRoot cause analysisProblem-solving

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

5 days ago

Sr. Supplier Quality Engineer

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 11 hours agoStatus: Live

Job Summary

Location: Costa Rica

Workplace: Hybrid

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Serve as the primary Supplier Quality Engineering point of contact for the Costa Rica facility, providing remote site support and aligning stakeholders across Quality, Manufacturing, R&D, Sustaining Engineering, and Procurement.
•Lead and own supplier quality documents and activities including MSA, PFMEA, Control Plan, SPC, PV&V, FAI, IQ/OQ/PQ, and APQP/PPAP to ensure process capability and compliance.
•Lead APQP/PPAP execution for supplier transfers, supplier changes, SICRs, and sustaining projects supporting the Costa Rica manufacturing facility.
•Facilitate Design for Excellence collaboration to improve design quality, manufacturability, supplier process robustness, and long-term product performance.
•Lead supplier audits and supplier qualification/approvals, and manage supplier non-conformance investigations and Supplier Corrective Action Requests (root cause, CAPA, verification, and closure).

Key Requirements

•7 years of experience in Quality, Manufacturing, or Supplier Quality Engineering, preferably in regulated industries such as medical devices.
•Strong expertise in supplier quality management, audits, root cause analysis, CAPA methodologies, process validation, and continuous improvement.
•Bachelor’s degree in Engineering, Supply Chain Management, Electrical/Electronic Engineering, or related field.
•Working knowledge of global medical device regulations and standards, with familiarity with statistical tools and quality methods.
•Strong cross-functional collaboration skills and a proactive, risk-based mindset.

Experience:7+ yearsMedical devicesRegulated industries

Education:Bachelor's in Engineering, Supply Chain Management, Electrical/Electronic Engineering, or a related field

Skills:Cross-functional collaborationRisk-based mindsetContinuous improvementRoot cause analysisProblem-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