Senior Regulatory Design Quality Engineer; Medical Devices
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Engineering
Medical Device Industry, Quality Engineering, Biomedical Engineer
Job Description & How to Apply Below
Symbios is seeking a Regulatory Affairs Design Quality Engineer to reinforce its regulatory and quality assurance team in the USA. The role focuses on handling regulatory interactions, design support, and ensuring compliance with EU and US requirements, including MDR and QMSR.
Ideal candidates have 7+ years in medical devices, experience with authorities and Notified Bodies, and strong risk management knowledge. Fluency in English and French is preferred, with Swiss-French ties noted.
For the Senior Regulatory Design Quality Engineer (Medical Devices) position at Symbios, we are reviewing applications now.
Consider building your career as a Senior Regulatory Design Quality Engineer (Medical Devices) at Symbios.
The Senior Regulatory Design Quality Engineer (Medical Devices) position in the Legal, Management & Operations field is open for applications.
We have an opening for a Senior Regulatory Design Quality Engineer (Medical Devices) in United States within Legal, Management & Operations.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).