Design QA & Risk Manager — Hybrid, Impactful Quality

Sonova Group; Schweiz; Hybrid; EUR 127.000 - 158.000; Vollzeit

Zusammenfassung

Sonova Communications, a leading provider of hearing-related solutions, seeks an experienced Quality Assurance Manager to join the Quality Assurance and Regulatory Affairs team in Murten. You will ensure non-medical products meet top quality standards throughout their lifecycle.

Your role includes owning QA processes, acting as DQA partner for R&D, and supporting audits to maintain ISO 9001 and ISO 13485 compliance, with a focus on continuous improvement and training.

Qualifikationen

• Engineering or scientific background in electronics, mechanics, physics, or related field.
• At least 5 years in Design Quality Assurance and risk management.
• Strong ISO 9001 knowledge; ISO 13485 is a plus.
• Background in consumer electronics or a comparable product-driven industry.
• Good English communication; German and/or French would be an advantage.

Aufgaben

• Own and continuously improve key quality processes, particularly risk management and CAPA.
• Act as Design Quality Assurance partner for R&D product development projects.
• Review and approve design and project documentation, ensuring compliance with internal processes, SOPs, and quality requirements.
• Ensure that verification and validation activities meet applicable quality requirements.
• Review and approve proposed changes to products already on the market.
• Support internal and external audits and contribute to maintaining compliance with ISO 9001 and ISO 13485.
• Promote a quality mindset through training, clear processes, KPIs, and continuous improvement activities.

Kenntnisse

Quality Assurance

Risk Management

English

German/French

Ausbildung

Engineering or science degree

Tools

QMS experience

Jobbeschreibung

Sonova Communications, a leading provider of hearing-related solutions, seeks an experienced Quality Assurance Manager to join the Quality Assurance and Regulatory Affairs team in Murten. You will ensure non-medical products meet top quality standards throughout their lifecycle.

Your role includes owning QA processes, acting as DQA partner for R&D, and supporting audits to maintain ISO 9001 and ISO 13485 compliance, with a focus on continuous improvement and training.