*Temporary position for 1 year + with an option for permanent work*
Characterizing and analyzing system requirements and providing systemic solutions for their implementation; Responsibility for secondary specifications and system requirements according to product requirements.
Leading technical discussions in multidisciplinary teams to find efficient solutions required in the life of the project
Responsibility for the integration of the system components throughout the product life cycle, including implementation at the customer, risk management, error budget analysis and troubleshooting.
Technical responsibility for system and engineering design and its execution; Responsibility for the systemic validation and verification program and performing proof of design (POD) tests.
Requirements:
Bachelor's degree in engineering – electronics/physics/biomedicine/machinery/aeronautics/software/ Computer Science
Master's degree in systems engineering – an advantage
Proven experience as a system Engineer, preferably in the medical device industry for at least 5 years.
Experience in developing systems under medical device regulation and standards.
Ability to communicate in English (written and verbal) mandatory
Develop and implement automation scripts to enhance efficiency in the deployment and maintenance of medical device systems (MATLAB, Python, etc.).
Experience with medical device software development lifecycle and regulatory requirements (e.g., ISO 13485, FDA regulations).
Familiarity with medical device communication protocols (e.g., DICOM, HL7).
Ability to work collaboratively in a team-oriented environment.
Excellent problem-solving and communication skills.
Bachelor's degree in engineering – electronics/physics/biomedicine/machinery/aeronautics/software/ Computer Science
Master's degree in systems engineering – an advantage
Proven experience as a system Engineer, preferably in the medical device industry for at least 5 years.
Experience in developing systems under medical device regulation and standards.
Ability to communicate in English (written and verbal) mandatory
Develop and implement automation scripts to enhance efficiency in the deployment and maintenance of medical device systems (MATLAB, Python, etc.).
Experience with medical device software development lifecycle and regulatory requirements (e.g., ISO 13485, FDA regulations).
Familiarity with medical device communication protocols (e.g., DICOM, HL7).
Ability to work collaboratively in a team-oriented environment.
Excellent problem-solving and communication skills.
This position is open to all candidates.
