Job Description:
Resolve the company products technical issues and continuously support and improve the products quality.
Managing technical ECOs to improve production processes.
Conduct technical investigations and experiments, drive for root cause identification as a part of the NCMR process.
Perform verification and validation activities for the production line.
Requirements
Education: 2nd year BSc student in mechanical engineering from a well-known establishment.
Understanding of assembling and manufacturing processes (injection molding, machining, PCB manufacturing etc.) – an advantage
Experience in the medical device industry and with FDA and ISO 13485 medical device regulations – an advantage.
Great problem-solving and debugging capabilities.
Availability for 24 hours a week.
Computer Skills:
Full control of all Microsoft Office applications.
SolidWorks.
Language skills: Fluent English (written and verbal)
Personality: Strong technical and analytical skills; excellent interpersonal relationships; self-motivated; independent; able to work under pressure; team player; 'out of the box' thinker.
