You ensure compliance and support design validation in R&D by collaborating with teams to manage risks and enhance quality throughout the development process.
Anforderungen
- •5+ years of experience in regulated industry
- •Bachelor’s or master’s degree in engineering
- •Knowledge of ISO 13485, ISO 14971, and MDR 2017/745
- •Hands-on experience with software development
- •Hands-on experience with design control
- •Excellent communication and stakeholder management skills
- •Proficient in MS Office; experience with tools like Visio
- •Detail-oriented, organised, and confident in influencing
- •Fluent in English; German is a plus
Deine Aufgaben
- •Ensure R&D process compliance with regulations.
- •Support user needs definition and design validation.
- •Assist with design FMEA and identify quality attributes.
- •Support design control for new development projects.
- •Perform risk management for assigned projects.
- •Collaborate with teams to identify quality issues early.
- •Support design changes and post-launch improvements.
- •Contribute to R&D process harmonization and standardization.
- •Assist with audits, non-conformances, and quality documentation.
Original Beschreibung
# Design Quality Assurance Engineer (Senior)
Join Sonova’s global quality team and play a key role in ensuring our innovative medical devices meet the highest standards of safety, performance, and compliance. As a **Design Quality Assurance Engineer (Senior)**, you’ll partner with R&D teams to guide product development from concept to launch, ensuring regulatory excellence every step of the way.
**Key Responsibilities**
* Ensure compliance of R&D processes with internal and external regulations
* Support definition of user needs and design validation activities
* Support with design FMEA activities and to identify critical to quality attributes
* Support design control activities for new development projects (Hardware/Software)
* Perform risk management activities for assigned projects
* Collaborate with development teams to prevent/identify quality issues early
* Support design changes and post-launch improvements
* Contribute to process harmonization and standardization across R&D
* Assist with audits, NCs, CAPAs, and quality documentation as required
**Your Profile**
* 5+ years of experience in a regulated industry, preferably medical devices
* Bachelor’s or master’s degree in engineering, science, quality is a plus
* Knowledge of ISO 13485, ISO 14971, and MDR 2017/745
* Hands-on experience with software development, IEC 62304/1, IEC60601 series is a plus
* Hands-on experience with design control, product risk management and design FMEA
* Excellent communication and stakeholder management skills
* Proficient in MS Office; experience with tools like Visio, Project, or Polarion is a plus
* Detail-oriented, organised, and confident in influencing without authority
* Fluent in English; German is a plus
## Sonova is an equal opportunity employer.
We team up. We grow talent. We collaborate with people of diverse backgrounds to win with the best team in the market place. We guarantee every person equal treatment in regard to employment and opportunity for employment, regardless of a candidate’s ethnic or national origin, religion, sexual orientation or marital status, gender, genetic identity, age, disability or any other legally protected status.
158248