Bern | Permanent employment with our customer
Reference number
My duties
  • Lead the design verification and validation activities including test planning and execution, and creation of protocols and reports
  • Be responsible for validation and statistical techniques in order to comply with associated regulatory requirements and internal standards
  • Serve as core team member on new Product Introduction projects to ensure compliance with design controls per ISO 13485 and FDA QSR
  • Be responsible of managing the company’s products Bill Of Material
  • Support reprocessing studies in areas such as cleaning, disinfection and sterilization according to relevant standards or regulations
My qualifications
  • A Bachelor or a higher degree in Mechanical Engineering, Biomedical Engineering or similar background
  • Well-founded experience in Design Assurance in medical device industry
  • Solid Works and PDM experience including technical drawings 
  • Good English level with strong technical writing skills
  • A person who thinks and works very organized and structured
My benefits
  • Take part in the development of the next generation of surgical robots!
  • A highly motivated team and an open way of communication
  • Permanent employment
About Hays
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
My contact at Hays

My contact person
Shirin Kim Weiss

Reference number

E-Mail: shirin.weiss@hays.ch