Requirements

Required education level
Bac. / Federal Vocational Bac., Ad. Federal PET / Fed. PET Diploma, Bachelor
Required experience
Between 1 and 3 years
Required language knowledge
English German
Required skills
Compliance production Manufacturing English Medical Devices German Engineering Cardiovascular MEDICAL DEVICES compliance DEVELOPMENT GERMAN Development medical devices engineering german english Medical devices ENGINEERING ISO 13485 manufacturing CARDIOVASCULAR validation cad cardiovascular German Validation ENGLISH CAD development Polymer ISO 9001 solidworks design SolidWorks polymer engineering Design Control MANUFACTURING COMPLIANCE Design Verification stent balloon catheter Solidworks Cagila Abaqus

Details

Location
Other countries
Term of employment
Full time
Sector
Medical technology
Professions
Management / Project Managemen... Laboratory / Analysis Medical-Technical Staff

Description

Development Engineers - Vascular products - design through verification, validation, & transfer to production - Switzerland - German/English speaker

Located in German speaking Switzerland, with excellent transport connections within mainland Europe, our client is a growing startup company already manufacturing it's own product, and actively developing new product on site.

Products are for the treatment of cardiovascular disease, hence experience with Class III vascular products is a huge bonus.

Day to day Tasks

  • Develop new product concepts and products
  • Design, develop and transfer new products into manufacturing
  • Support design control activities such as risk analysis, product specification, test method and process development to successfully bring product through design verification & validation to design transfer stage
  • Ensure that all products and processes are developed in compliance with regulatory requirements and best practise
  • Actively participating on design teams, understand R&D goals and time lines
  • Review and knowledge of literature and intellectual property
  • Create, review and coordinate test protocols and reports

Typically we'd expect to see a Bachelor's degree in engineering or master's degree in applied science together with 3-5 years of product development experience (design / verification / validation / transfer to production), within the medical device industry. A working knowledge of materials used in the cardio-vascular medical device industry is a huge benefit, as is an in depth knowledge on the new MDR, ICH, GMP and relevant international regulations.
Business level German and English are required because of internal documentation and German speaking locality.

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 80 816, and email him at quality@nonstop-devices.com

KEY WORDS: Feasibility, Concept, Design, Development, Validation, Verification, Risk Management, Compliance, Production, Manufacturing, materials science, Medical Devices, German, English, ISO 13485, ISO 9001, Mechanical Engineering, cardiovascular, 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
Not available

Contact info

NonStop Consulting
Andrew Boroky
10w yw y- z7 )y( 07g
Not available