Sonova

2 weeks ago

Supplier Quality Engineer - Mechanics (Singapore, Singapore)

✓ 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 improving and harmonizing supplier quality for mechanical components. Own supplier quality assurance and control activities, monitor performance indicators, and act as the central contact for nonconformities, escalations, containment, and root-cause investigations. Develop supplier performance controls, evaluate capability, coordinate 8D/SCAR and CAPA actions, and support audits plus part/process qualification while driving global process harmonization.

Location: Singapore

Workplace: Hybrid

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Support supplier quality assurance and control activities by monitoring performance indicators to ensure compliance with quality requirements and international regulations.
•Process nonconformities and lead resolution of supplier quality issues and escalations, including containment actions and root cause investigations.
•Implement Supplier Quality Management (SQM) requirements and drive preventative measures to improve supplier performance transparency.
•Evaluate supplier performance and capability, and coordinate 8D/SCAR reports and CAPA actions in collaboration with specialist departments.
•Support supplier audits and new supplier activities, including part and process qualification and validation, and drive global process harmonization.

Travel: Medium travel

Pay and Benefits

Perks:Hybrid Work

Key Requirements

•6+ years of experience in a medical device manufacturing environment in a quality-related role, including supplier quality management and contract manufacturing.
•In-depth knowledge of ISO 13485 and ISO 9001; knowledge of QSR 820, MDSAP, and MDR is a plus.
•Proven expertise in plastic injection molding, polymers, resins, lacquering, coating, and related technologies for mechanical components.
•Essential experience with 8D/SCAR methodologies, quality reports, improvement programs, and supplier audits.
•Fluent English (written and spoken) and advanced MS Office skills; comfort managing projects.

Experience:6+ yearsMedical devicesSupplier quality managementContract manufacturing

Education:Master's

Skills:CommunicationProject managementAttention to detailOrganizationReliability

Languages:EnglishVietnameseGerman

Tech Stack:ISO 13485ISO 9001QSR 820MDSAPMDR8D/SCARCAPAMS 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 - Mechanics (Singapore, Singapore)

✓ 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 assurance and control activities by monitoring performance indicators to ensure compliance with quality requirements and international regulations.
•Process nonconformities and lead resolution of supplier quality issues and escalations, including containment actions and root cause investigations.
•Implement Supplier Quality Management (SQM) requirements and drive preventative measures to improve supplier performance transparency.
•Evaluate supplier performance and capability, and coordinate 8D/SCAR reports and CAPA actions in collaboration with specialist departments.
•Support supplier audits and new supplier activities, including part and process qualification and validation, and drive global process harmonization.

Travel: Medium travel

Pay and Benefits

Perks:Hybrid Work

Key Requirements

•6+ years of experience in a medical device manufacturing environment in a quality-related role, including supplier quality management and contract manufacturing.
•In-depth knowledge of ISO 13485 and ISO 9001; knowledge of QSR 820, MDSAP, and MDR is a plus.
•Proven expertise in plastic injection molding, polymers, resins, lacquering, coating, and related technologies for mechanical components.
•Essential experience with 8D/SCAR methodologies, quality reports, improvement programs, and supplier audits.
•Fluent English (written and spoken) and advanced MS Office skills; comfort managing projects.

Experience:6+ yearsMedical devicesSupplier quality managementContract manufacturing

Education:Master's

Skills:CommunicationProject managementAttention to detailOrganizationReliability

Languages:EnglishVietnameseGerman

Tech Stack:ISO 13485ISO 9001QSR 820MDSAPMDR8D/SCARCAPAMS 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