Required education level
Bac. / Federal Vocational Bac., Ad. Federal PET / Fed. PET Diploma, Bachelor
Required experience
Between 3 and 5 years
Required language knowledge
English German
Required skills
Compliance Design Manufacturing English German Engineering compliance DEVELOPMENT GERMAN Development engineering german english ENGINEERING ISO 13485 manufacturing production validation cad German Validation ENGLISH CAD design TECHNICAL development Production ISO 9001 solidworks PRODUCTION Technical design technical SolidWorks engineering Design Control medical devices MANUFACTURING documentation COMPLIANCE Verification Solidworks electromechanical product support Medical Devices design control


Other countries
Term of employment
Full time
Medical technology
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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

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.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

NonStop Consulting
Mar 29, 2021

Contact info

NonStop Consulting
Andrew Boroky
p0w yw y- z7 )y( 07g
Not available