Systems Engineering/Electronics Development/Lifecycle management - Zurich MedTech - English essential
Based in Zurich, our client is a small, developer and manufacturer of a Class III medical device doing well in Europe and ramping up production for imminent release into the USA. The person would be part of a growing team tasked with ensuring supply of product leading up to release and beyond. That growing team consists of mechanical engineers, software engineers, lifecycle engineers, biomedical Engineers and development engineers. On their wanted list now is someone bringing strong electronics engineering experience (5 yrs+) for activities ranging from hands on coordination of projects, troubleshooting, verification and validation, change management and documentation, supporting manufacturing to ensure continued availability of the product, and acting as the technical Subject matter expert for Quality, Regulatory, and Development areas within the Business.
Medical Device development experience is essential and ideally with Class III electromechanical products (Class II acceptable also). The position is new and permanent and comes during an exciting period of growth over the last year.
A good working knowledge of Quality standards ISO 13485, ISO 62304, FDA equivalents is desirable, but this is not a Quality role. Fluent English is essential both as the local spoken language but also for documentation purposes, which are an important part of this role.
This is a terrific opportunity to join a company at the ground level and during a strong growth cycle and help deliver products to market that significantly improve a patient's quality of life.
If this sounds like you, please contact the Senior Consultant Andrew Boroky for more information on 0041 43 50 80 817, and email him at email@example.com
KEY WORDS: Development, Validation, Verification, Risk Management, Compliance, electromechanical, hardware, software, firmware, product support, documentation, technical, Design Control, Manufacturing, Change control, Medical Devices, German, English, ISO 13485, IEC 62304, code development, code review, Integrated Development Environments, software release management, bu software test platforms, Engineering, Production, Medical Device jobs, Nonstop recruitment.
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