Sonova

2 weeks ago

Supplier Quality Engineer - Electronics

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 6 hours agoStatus: Live

Job Summary

Support the SQM team in supplier quality improvement and harmonization by applying quality tools and problem-solving methodologies to resolve supplier quality issues and escalations. Develop and monitor supplier performance control requirements to improve transparency of cost to poor quality and ensure compliance with quality regulations. Act as a point of contact for supplier quality concerns, process nonconformities (8D/SCAR), and coordinate corrective/preventive actions, audits, and new supplier activities.

Location: Singapore

Workplace: Hybrid

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Support supplier quality improvement and harmonization activities using quality tools and problem-solving methodologies.
•Develop, maintain, monitor, and ensure supplier performance control requirements to improve transparency of cost to poor quality and ensure regulatory compliance.
•Support supplier quality assurance and control by monitoring performance indicators against quality requirements and international regulations.
•Process supplier nonconformities, ensuring containment actions, root cause investigations, and preventative measures are implemented.
•Process 8D/SCAR reports and coordinate corrective/preventive actions, supplier audits, and new supplier activities including part and process qualification and validation.

Travel: High travel

Key Requirements

•Graduate degree in engineering, science, quality, or a technical field, or 8+ years of supplier quality management experience.
•Minimum 6 years in a medical device manufacturing quality-related role, with supplier quality management and contract manufacturing experience.
•In-depth knowledge of ISO 13485 and ISO 9001, with knowledge of QSR 820, MDSAP, and MDR as a plus.
•Strong technical knowledge of electronic commodities (batteries, PCBs, chargers, electro-mechanics) and production technologies for electronic components.
•Essential experience with 8D/SCAR methodologies, quality reports, improvement programs, and supplier audits; fluent English required; advanced MS Office required.

Experience:6+ yearsMedical devicesMedical device manufacturingSupplier quality managementContract manufacturing

Education:Master's

Skills:Self-confidentWell-organizedReliableAttention to detailTeam collaboration

Languages:EnglishVietnameseGerman

Tech Stack:ISO 13485ISO 9001QSR 820MDSAPMDR8DSCARMS Office

Company Brief

Sonova

Designs, manufactures, and distributes hearing care solutions including hearing aids, cochlear implant accessories, and wireless communication devices, serving audiologists and consumers worldwide through clinics, retail networks, and distribution partners.

Industry: Medical Devices

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Stäfa, Switzerland

Founded: 1947

Website

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Sonova

2 weeks ago

Supplier Quality Engineer - Electronics

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 6 hours agoStatus: Live

Job Summary

Location: Singapore

Workplace: Hybrid

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Support supplier quality improvement and harmonization activities using quality tools and problem-solving methodologies.
•Develop, maintain, monitor, and ensure supplier performance control requirements to improve transparency of cost to poor quality and ensure regulatory compliance.
•Support supplier quality assurance and control by monitoring performance indicators against quality requirements and international regulations.
•Process supplier nonconformities, ensuring containment actions, root cause investigations, and preventative measures are implemented.
•Process 8D/SCAR reports and coordinate corrective/preventive actions, supplier audits, and new supplier activities including part and process qualification and validation.

Travel: High travel

Key Requirements

•Graduate degree in engineering, science, quality, or a technical field, or 8+ years of supplier quality management experience.
•Minimum 6 years in a medical device manufacturing quality-related role, with supplier quality management and contract manufacturing experience.
•In-depth knowledge of ISO 13485 and ISO 9001, with knowledge of QSR 820, MDSAP, and MDR as a plus.
•Strong technical knowledge of electronic commodities (batteries, PCBs, chargers, electro-mechanics) and production technologies for electronic components.
•Essential experience with 8D/SCAR methodologies, quality reports, improvement programs, and supplier audits; fluent English required; advanced MS Office required.

Experience:6+ yearsMedical devicesMedical device manufacturingSupplier quality managementContract manufacturing

Education:Master's

Skills:Self-confidentWell-organizedReliableAttention to detailTeam collaboration

Languages:EnglishVietnameseGerman

Tech Stack:ISO 13485ISO 9001QSR 820MDSAPMDR8DSCARMS Office

Company Brief

Sonova

Industry: Medical Devices

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Stäfa, Switzerland

Founded: 1947

Website