Töösisu kirjeldus
Creation of system requirements and system architecture for single use medical devices
Responsible for ensuring the traceability according to ISO 13485
Taking the technical lead within a project team
Participation and Cooperation with other specialist teams throughout the development process
Analyzing synergies between related products and enhancing effectiveness in the development process
Consideration of the balance between costs, development time and technical solutions for single-use products
Ootused kandidaadile
Successfully completed studies in medical engineering, electrical engineering, mechatronics, physical engineering or a similar degree program
Experience/know-how in the field of medical device development and the relevant standards (IEC60601-1, ISO14971) desirable
Initial experience with either topic such as Design Control, Sterile Single Use products, HW development, Signal processing (FPGAs) desirable
Initial experience of requirements management and its tools such as PTC, DOORS, Polarion or similar desirable
Teamwork is a central element of your work and your actions
Very good analytical and problem-solving skills
Business fluent in written and spoken English. Estonian language would be beneficial
Please submit your CV in English
Kandideerimine
Kandideerimine kestab kandideerimisperioodi lõpuni.